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1. Mahajan S, Srikant N, Boaz K, George T: Osteoblastoma of maxilla with cartilaginous matrix: review of literature and report of a case. Singapore Dent J; 2007 Dec;29(1):12-8
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  • [Title] Osteoblastoma of maxilla with cartilaginous matrix: review of literature and report of a case.
  • Osteoblastoma is a rare benign neoplasm of jaws.
  • We report a case of a recurrent osteoblastoma in the maxilla of a 34-year-old male who presented with aggressive clinical and histologic features: namely root resorption, tooth mobility, involvement of maxillary sinus, chondroid formation, host bone trapping, and lack of osteoblastic rimming.
  • A systematic review of other reported cases of osteoblastoma of jaws with a note on the recurrent cases has been put forth.
  • [MeSH-major] Cartilage / pathology. Maxillary Neoplasms / pathology. Osteoblastoma / pathology
  • [MeSH-minor] Adult. Connective Tissue / pathology. Diagnosis, Differential. Humans. Male. Maxillary Sinus / pathology. Neoplasm Invasiveness. Neoplasm Recurrence, Local / pathology. Osteoblasts / pathology

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  • (PMID = 18472525.001).
  • [ISSN] 0377-5291
  • [Journal-full-title] Singapore dental journal
  • [ISO-abbreviation] Singapore Dent J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Singapore
  • [Number-of-references] 18
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2. Cleton-Jansen AM, Anninga JK, Briaire-de Bruijn IH, Romeo S, Oosting J, Egeler RM, Gelderblom H, Taminiau AH, Hogendoorn PC: Profiling of high-grade central osteosarcoma and its putative progenitor cells identifies tumourigenic pathways. Br J Cancer; 2009 Dec 1;101(11):1909-18
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  • BACKGROUND: Osteosarcoma is the most prevalent primary malignant bone tumour in children and young adults, with poor survival in 40% of patients.
  • Comparing benign osteoblastomas with osteosarcomas identified cell cycle regulation as the most prominently changed pathway.
  • Gene expression differences between highly malignant osteosarcoma and benign osteoblastoma involve cell cycle regulation.
  • [MeSH-major] Bone Neoplasms / pathology. Mesenchymal Stromal Cells / pathology. Neoplastic Stem Cells / pathology. Osteosarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Cell Cycle / physiology. Cell Differentiation. Cell Line, Tumor. Child. Child, Preschool. Down-Regulation. Female. Gene Expression Profiling. Humans. Male. Osteoblastoma / genetics. Osteoblastoma / metabolism. Osteoblastoma / pathology. Signal Transduction. Up-Regulation. Wnt Proteins / genetics. Wnt Proteins / metabolism. Young Adult

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  • [Cites] Trends Genet. 2000 Jul;16(7):279-83 [10858654.001]
  • [Cites] J Natl Cancer Inst. 2007 Jan 17;99(2):98-9 [17227987.001]
  • [Cites] J Clin Pathol. 2001 Oct;54(10):778-82 [11577126.001]
  • [Cites] J Clin Oncol. 2002 Feb 1;20(3):776-90 [11821461.001]
  • [Cites] Clin Orthop Relat Res. 2002 Apr;(397):40-52 [11953594.001]
  • [Cites] Nat Genet. 2002 May;31(1):19-20 [11984561.001]
  • [Cites] Biostatistics. 2003 Apr;4(2):249-64 [12925520.001]
  • [Cites] Int J Oncol. 2004 Mar;24(3):647-55 [14767549.001]
  • [Cites] Bioinformatics. 2004 Feb 12;20(3):307-15 [14960456.001]
  • [Cites] Pathol Res Pract. 1998;194(10):679-84 [9820863.001]
  • [Cites] J Cell Biochem. 2004 Dec 15;93(6):1210-30 [15486964.001]
  • [Cites] Bioinformatics. 2004 Dec 12;20(18):3705-6 [15297296.001]
  • [Cites] Bioinformatics. 2005 Jan 15;21(2):171-8 [15308542.001]
  • [Cites] J Pathol. 2005 Mar;205(4):476-82 [15685701.001]
  • [Cites] J Clin Oncol. 2005 Mar 1;23(7):1483-90 [15735124.001]
  • [Cites] J Natl Cancer Inst. 2007 Jan 17;99(2):112-28 [17227995.001]
  • [Cites] Stem Cells. 2007 Feb;25(2):371-9 [17038675.001]
  • [Cites] Connect Tissue Res. 2007;48(3):132-40 [17522996.001]
  • [Cites] Dev Biol. 2007 Jun 1;306(1):121-33 [17433286.001]
  • [Cites] J Cell Biochem. 2007 Aug 1;101(5):1109-24 [17546602.001]
  • [Cites] Cancer Res. 2007 Oct 1;67(19):9142-9 [17909019.001]
  • [Cites] Nat Rev Cancer. 2008 May;8(5):387-98 [18432252.001]
  • [Cites] J Pathol. 2010 Jan;220(1):24-33 [19882675.001]
  • [Cites] Cancer Res. 2005 Mar 1;65(5):1748-54 [15753370.001]
  • [Cites] Cancer Res. 2005 Sep 15;65(18):8142-50 [16166288.001]
  • [Cites] J Clin Oncol. 2005 Oct 10;23(29):7257-64 [16087957.001]
  • [Cites] Trends Cell Biol. 2006 Mar;16(3):151-8 [16466918.001]
  • [Cites] Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5923-8 [16585533.001]
  • [ErratumIn] Br J Cancer. 2009 Dec 15;101(12):2064
  • (PMID = 19888226.001).
  • [ISSN] 1532-1827
  • [Journal-full-title] British journal of cancer
  • [ISO-abbreviation] Br. J. Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Wnt Proteins
  • [Other-IDs] NLM/ PMC2788255
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3. Chadha M, Agarwal A, Wadhwa N: Chondroid chordoma of the L5 spinous process and lamina: a case report. Eur Spine J; 2005 Oct;14(8):803-6
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  • Chordoma is a rare bone tumor that originates from the remnants of the notochord.
  • A differential diagnosis of a benign tumor (giant cell tumor, aneurysmal bone cyst or osteoblastoma) was made initially.
  • [MeSH-major] Chordoma / pathology. Diagnosis, Differential. Lumbar Vertebrae / pathology

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  • [Cites] Spine (Phila Pa 1976). 2000 Oct 1;25(19):2537-40 [11013508.001]
  • [Cites] Spine (Phila Pa 1976). 2001 Jan 1;26(1):27-35 [11148642.001]
  • [Cites] J Neurosurg. 2001 Apr;94(2 Suppl):284-91 [11302633.001]
  • [Cites] Am J Surg Pathol. 2004 Jun;28(6):756-61 [15166667.001]
  • [Cites] Eur Spine J. 1994;3(2):115-7 [7874548.001]
  • [Cites] Spine (Phila Pa 1976). 1996 Jul 1;21(13):1569-77 [8817786.001]
  • [Cites] Am J Clin Pathol. 1995 Mar;103(3):271-9 [7532910.001]
  • [Cites] Cancer. 1973 Aug;32(2):410-20 [4722921.001]
  • [Cites] Clin Oncol. 1984 Jun;10(2):167-72 [6734008.001]
  • [Cites] Skeletal Radiol. 1986;15(3):242-6 [3790204.001]
  • [Cites] Histopathology. 1987 Aug;11(8):775-87 [3305286.001]
  • [Cites] J Spinal Disord. 1989 Jun;2(2):69-74 [2520065.001]
  • [Cites] Cancer. 1993 Nov 15;72(10):2943-9 [7693324.001]
  • [Cites] Spine (Phila Pa 1976). 1997 May 1;22(9):1036-44 [9152458.001]
  • (PMID = 15895260.001).
  • [ISSN] 0940-6719
  • [Journal-full-title] European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
  • [ISO-abbreviation] Eur Spine J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Other-IDs] NLM/ PMC3489257
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4. Harrop JS, Schmidt MH, Boriani S, Shaffrey CI: Aggressive "benign" primary spine neoplasms: osteoblastoma, aneurysmal bone cyst, and giant cell tumor. Spine (Phila Pa 1976); 2009 Oct 15;34(22 Suppl):S39-47
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  • [Title] Aggressive "benign" primary spine neoplasms: osteoblastoma, aneurysmal bone cyst, and giant cell tumor.
  • OBJECTIVE: To define optimal clinical care for primary spinal aggressive "benign" osseous neoplasms using a systematic review with expert opinion.
  • METHODS: Predefined focused questions on treatment of osteoblastomas, aneurysmal bone cysts and giant cell tumors were refined by a panel of spine oncology surgeons, medical and radiation oncologist.
  • The osteoblastoma initial search identified 211 articles of which 17 were pertinent to the spinal questions.
  • The aneurysmal bone cysts initial search revealed 482 articles initially of which 6 were pertinent; and the search on giant cell tumors identified 178 articles of which only 8 were focused on the predefined treatment questions.
  • CONCLUSION: Spinal aggressive benign osseous neoplasms have varying histology.
  • [MeSH-major] Bone Cysts, Aneurysmal / therapy. Giant Cell Tumor of Bone / therapy. Osteoblastoma / therapy. Spinal Diseases / therapy. Spinal Neoplasms / therapy

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  • (PMID = 19829276.001).
  • [ISSN] 1528-1159
  • [Journal-full-title] Spine
  • [ISO-abbreviation] Spine
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 82
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5. Mortazavi SM, Wenger D, Asadollahi S, Shariat Torbaghan S, Unni KK, Saberi S: Periosteal osteoblastoma: report of a case with a rare histopathologic presentation and review of the literature. Skeletal Radiol; 2007 Mar;36(3):259-64
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  • [Title] Periosteal osteoblastoma: report of a case with a rare histopathologic presentation and review of the literature.
  • Osteoblastoma is an uncommon benign bone tumor most commonly located in the vertebral column or metaphysis of a long bone.
  • We report a periosteal-based osteoblastoma, arising from the proximal tibia, in a 20-year-old woman who presented with knee swelling and pain of 2-year duration.
  • Histopathologic evaluation disclosed immature bone and osteoid deposition in a vascularized stroma, associated with numerous osteoblasts and osteoclasts rimming the bony trabeculae.
  • Although extremely unusual, the presence of cartilage does not necessarily exclude the diagnosis of osteoblastoma.
  • [MeSH-major] Bone Neoplasms / diagnosis. Knee Joint / pathology. Osteoblastoma / diagnosis. Periosteum / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Tomography, Emission-Computed. Tomography, X-Ray Computed

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  • [Cites] Am J Surg Pathol. 1996 Jul;20(7):841-50 [8669532.001]
  • [Cites] Skeletal Radiol. 1989;18(7):551-5 [2588037.001]
  • [Cites] Clin Orthop Relat Res. 1989 Mar;(240):281-310 [2537165.001]
  • [Cites] J Bone Joint Surg Am. 1994 Mar;76(3):366-78 [8126042.001]
  • [Cites] Am J Surg Pathol. 1993 Jan;17 (1):69-74 [8447510.001]
  • [Cites] Radiology. 1990 Jun;175(3):783-90 [2343130.001]
  • [Cites] AJR Am J Roentgenol. 1976 Feb;126(2):321-5 [175701.001]
  • [Cites] Arch Pathol Lab Med. 2005 Jun;129(6):787-9 [15913430.001]
  • [Cites] Acta Orthop Scand. 1970;41(3):272-91 [5486182.001]
  • [Cites] Skeletal Radiol. 2004 Feb;33(2):107-11 [14714148.001]
  • [Cites] Pathol Int. 2000 Aug;50(8):667-71 [10972867.001]
  • [Cites] J Bone Joint Surg Am. 1964 Jun;46:755-65 [14161088.001]
  • [Cites] J Orthop Sci. 1998;3(6):341-5 [9811987.001]
  • [Cites] Semin Diagn Pathol. 1984 Aug;1(3):215-34 [6600112.001]
  • [Cites] Orthopedics. 1999 Feb;22(2):244-7; quiz 248-9 [10037340.001]
  • [Cites] J Laryngol Otol. 1978 Apr;92(4):337-45 [641417.001]
  • [Cites] J Bone Joint Surg Am. 1983 Feb;65(2):205-12 [6822582.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Br J Oral Surg. 1976 Jul;14(1):12-22 [1066151.001]
  • [Cites] AJR Am J Roentgenol. 2004 May;182(5):1343-4 [15868703.001]
  • [Cites] Clin Orthop Relat Res. 1982 Jul;(167):222-35 [7094467.001]
  • [Cites] Am J Clin Pathol. 1971 Jul;56(1):73-8 [5283284.001]
  • [Cites] Am J Surg Pathol. 1985 Sep;9(9):666-77 [4051099.001]
  • (PMID = 16868789.001).
  • [ISSN] 0364-2348
  • [Journal-full-title] Skeletal radiology
  • [ISO-abbreviation] Skeletal Radiol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 29
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6. Capodiferro S, Maiorano E, Giardina C, Lacaita MG, Lo Muzio L, Favia G: Osteoblastoma of the mandible: clinicopathologic study of four cases and literature review. Head Neck; 2005 Jul;27(7):616-21
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  • [Title] Osteoblastoma of the mandible: clinicopathologic study of four cases and literature review.
  • BACKGROUND: Osteoblastoma is a benign bone tumor accounting for 1% of all bone tumors; it commonly involves the spine and the sacrum of young individuals, with less than 5% being localized to the posterior mandible.
  • In view of its rarity in the maxilla and mandible, osteoblastoma is rarely diagnosed as such in the absence of interdisciplinary cooperation.
  • METHODS: A retrospective study of four benign osteoblastomas was performed based on a review of the clinical, radiographic, and histopathologic features of all cases.
  • RESULTS: The tumors involved the posterior mandible of young patients (age range, 10-21 years; two male and two female patients) and appeared as painful bone expansions.
  • Histologically, they were composed of osteoid and woven bone surrounded by plump osteoblast-like cells with interposed fibroblasts, inflammatory cells, and red blood cells.
  • CONCLUSIONS: Osteoblastomas may be distinguished from other bone tumors, fibro-osseous lesions, and odontogenic neoplasms on the basis of integrated clinical, radiologic, and histologic features and usually manifest an indolent clinical course.
  • [MeSH-major] Mandibular Neoplasms / pathology. Osteoblastoma / pathology
  • [MeSH-minor] Adolescent. Adult. Child. Diagnosis, Differential. Female. Humans. Male. Retrospective Studies. Tomography, X-Ray Computed

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  • (PMID = 15880408.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 20
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7. Sidani CA, Karam AR, Bruce JH, Sklar E: Osteoblastoma of the frontal sinuses presenting with headache and blurred vision: case report and review of the literature. J Radiol Case Rep; 2010;4(6):1-7
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  • [Title] Osteoblastoma of the frontal sinuses presenting with headache and blurred vision: case report and review of the literature.
  • Osteoblastoma is a rare benign bone tumor that usually arises in the vertebral column and long bones of young adults.
  • To date, osteoblastoma of the frontal sinus has not been reported in the English literature.
  • We report an osteoblastoma of both frontal sinuses in a 23-year-old male who presented with headache and blurry vision in the left eye.
  • Surgical resection was performed and histology was consistent with osteoblastoma.

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  • (PMID = 22470734.001).
  • [ISSN] 1943-0922
  • [Journal-full-title] Journal of radiology case reports
  • [ISO-abbreviation] J Radiol Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC3303412
  • [Keywords] NOTNLM ; Frontal sinus / exophthalmos / osteoblastoma
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8. Manjunatha BS, Nagarajappa D: Osteoid osteoma. Indian J Dent Res; 2009 Oct-Dec;20(4):514-5
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  • Osteoid osteoma is a benign tumor of the bone which arises from osteoblasts and is extremely rare in jaws.
  • [MeSH-major] Mandibular Neoplasms / diagnosis. Osteoma, Osteoid / diagnosis
  • [MeSH-minor] Adolescent. Diagnosis, Differential. Female. Fibroma, Ossifying / diagnosis. Humans. Mandibular Diseases / diagnosis. Osteitis / diagnosis. Osteoblastoma / diagnosis

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  • (PMID = 20139585.001).
  • [ISSN] 1998-3603
  • [Journal-full-title] Indian journal of dental research : official publication of Indian Society for Dental Research
  • [ISO-abbreviation] Indian J Dent Res
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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9. Avadhanam PK, Vuyyur S, Panigrahi MK: A rare occurrence of osteoblastoma in a child. J Pediatr Neurosci; 2010 Jul;5(2):153-6
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  • [Title] A rare occurrence of osteoblastoma in a child.
  • To report a rare occurrence of osteoblastoma involving the L4 vertebra in an 8-year-old female child with histological features suggestive of osteoblastoma with secondary aneurysmal changes.
  • The mean age incidence of osteoblastoma is 20.4 years.
  • In our case, a rare presentation of osteoblastoma was seen in the first decade.
  • Osteoblastoma is a rare tumor with an incidence of 1% of all tumors and 30-40% of cases involving the spine.
  • Osteoblastoma occurs most commonly in males (M:F, 2.5:1).

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  • [Cites] Neurol India. 1999 Dec;47(4):330-1 [10625912.001]
  • [Cites] J Pediatr Orthop. 1994 Nov-Dec;14(6):788-92 [7814596.001]
  • [Cites] Cancer. 1956 Sep-Oct;9(5):1044-52 [13364889.001]
  • [Cites] Clin Orthop Relat Res. 1992 May;(278):37-45 [1563167.001]
  • [Cites] Neurol Med Chir (Tokyo). 2005 Jul;45(7):379-83 [16041187.001]
  • [Cites] Surg Neurol. 1992 Jul;38(1):12-8 [1615369.001]
  • [Cites] J Bone Joint Surg Am. 1986 Mar;68(3):354-61 [3949831.001]
  • [Cites] Orthop Clin North Am. 1996 Jul;27(3):559-74 [8649737.001]
  • [Cites] Med Pediatr Oncol. 1997 Apr;28(4):305-9 [9078333.001]
  • [Cites] J Spinal Disord. 1992 Jun;5(2):204-11 [1606380.001]
  • [Cites] AJR Am J Roentgenol. 1976 Feb;126(2):321-5 [175701.001]
  • [Cites] Cancer. 1991 Sep 1;68(5):999-1003 [1913494.001]
  • [Cites] J Spinal Disord. 1990 Jun;3(2):179-82 [2134427.001]
  • [Cites] Spine (Phila Pa 1976). 1990 Dec;15(12):1272-80 [2149206.001]
  • [Cites] J Neurosurg. 1988 Jun;68(6):884-8 [2453621.001]
  • [Cites] Surg Neurol. 1987 Apr;27(4):381-5 [3824145.001]
  • [Cites] Clin Orthop Relat Res. 1986 Mar;(204):76-85 [3956019.001]
  • [Cites] J Bone Joint Surg Br. 1973 Nov;55(4):841-7 [4766190.001]
  • [Cites] Clin Orthop Relat Res. 1974 Jan-Feb;(98):225-30 [4817234.001]
  • [Cites] J Neurosurg. 1969 Oct;31(4):468-73 [5349094.001]
  • [Cites] Neurosurgery. 1981 Jan;8(1):31-8 [7207770.001]
  • [Cites] J Bone Joint Surg Am. 1975 Jan;57(1):1-9 [1123354.001]
  • (PMID = 21559167.001).
  • [ISSN] 1998-3948
  • [Journal-full-title] Journal of pediatric neurosciences
  • [ISO-abbreviation] J Pediatr Neurosci
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3087998
  • [Keywords] NOTNLM ; Benign tumors of spine / osteoblastoma / osteoblastoma in childhood
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10. Muzumdar D, Balasubramaniam S, Jhawar S, Goel A: Massive benign osteoblastoma of the suboccipital bone and foramen magnum region. Pediatr Neurosurg; 2010;46(3):232-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Massive benign osteoblastoma of the suboccipital bone and foramen magnum region.
  • Benign osteoblastoma is an uncommon primary bone tumor frequently found in the vertebral column and long tubular bones, and rarely occurring in the calvarium.
  • A case of a massive benign osteoblastoma of the suboccipital bone and foramen magnum region in a 9-year-old boy is reported.
  • The occurrence of benign osteoblastoma in the suboccipital bone and foramen magnum region has not been reported earlier in the pediatric population.
  • [MeSH-major] Foramen Magnum / surgery. Occipital Bone / surgery. Osteoblastoma / surgery. Skull Neoplasms / surgery

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  • [Copyright] Copyright © 2010 S. Karger AG, Basel.
  • (PMID = 21051923.001).
  • [ISSN] 1423-0305
  • [Journal-full-title] Pediatric neurosurgery
  • [ISO-abbreviation] Pediatr Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
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11. von Chamier G, Holl-Wieden A, Stenzel M, Raab P, Darge K, Girschick HJ, Beer M: Pitfalls in diagnostics of hip pain: osteoid osteoma and osteoblastoma. Rheumatol Int; 2010 Jan;30(3):395-400
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pitfalls in diagnostics of hip pain: osteoid osteoma and osteoblastoma.
  • Osteoid osteoma and osteoblastoma are benign bone tumors that occur most often in adolescents and predominantly in males.
  • Typical clinical symptoms, such as reduced range of motion of adjacent joints, nocturnal bone pain and relief of pain using non-steroidal anti-inflammatory drug therapy especially in osteoid osteoma may lead to the correct diagnosis.
  • In radiographic examinations, the initial changes are often uncharacteristic causing further delay in diagnosis.
  • Magnetic resonance imaging is increasingly used for screening, but early findings in the course of disease might not lead to the definite diagnosis.
  • To demonstrate pitfalls in the diagnostic pathway of hip pain caused by benign bone tumors, we present two cases with osteoid osteoma and one with osteoblastoma.
  • [MeSH-major] Arthralgia / etiology. Bone Neoplasms / pathology. Diagnostic Errors / prevention & control. Hip Joint / pathology. Osteoblastoma / pathology. Osteoma, Osteoid / pathology
  • [MeSH-minor] Adolescent. Anti-Inflammatory Agents, Non-Steroidal / therapeutic use. Arthrography. Child. Diagnosis, Differential. Female. Femur Neck / diagnostic imaging. Femur Neck / pathology. Humans. Magnetic Resonance Imaging / methods. Male. Predictive Value of Tests. Sensitivity and Specificity. Synovial Membrane / diagnostic imaging. Synovial Membrane / pathology. Ultrasonography

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  • [Cites] Ann Rheum Dis. 2005 Feb;64(2):279-85 [15647436.001]
  • [Cites] N Engl J Med. 2007 Nov 29;357(22):2277-84 [18046031.001]
  • [Cites] Acta Radiol. 2001 Jan;42(1):6-9 [11167323.001]
  • [Cites] Top Magn Reson Imaging. 2002 Aug;13(4):219-29 [12409690.001]
  • [Cites] Clin Orthop Relat Res. 2005 Apr;(433):171-7 [15805954.001]
  • [Cites] Clin Imaging. 2000 Jan-Feb;24(1):19-27 [11120413.001]
  • [Cites] Radiology. 1990 Jun;175(3):783-90 [2343130.001]
  • [Cites] Radiology. 1993 Jan;186(1):227-32 [8416569.001]
  • [Cites] Arch Orthop Trauma Surg. 2006 Dec;126(10):660-7 [16927097.001]
  • [Cites] Radiology. 2003 Jun;227(3):691-700 [12773675.001]
  • [Cites] Radiology. 2003 Oct;229(1):171-5 [12944597.001]
  • [Cites] Radiographics. 1992 Nov;12(6):1119-34; discussion 1135-6 [1439015.001]
  • [Cites] J Bone Joint Surg Br. 1999 Sep;81(5):814-20 [10530842.001]
  • [Cites] Clin Radiol. 2003 Nov;58(11):845-52 [14581007.001]
  • [Cites] Am J Surg Pathol. 1991 Apr;15(4):381-7 [2006718.001]
  • [Cites] Magn Reson Imaging Clin N Am. 2005 Nov;13(4):757-74 [16275582.001]
  • [Cites] Skeletal Radiol. 1993 Oct;22(7):485-500 [8272884.001]
  • [Cites] Radiology. 1994 Apr;191(1):217-23 [8134575.001]
  • [Cites] Skeletal Radiol. 2002 Oct;31(10):559-69 [12324824.001]
  • [Cites] J Child Neurol. 2007 Feb;22(2):170-5 [17621478.001]
  • (PMID = 19444452.001).
  • [ISSN] 1437-160X
  • [Journal-full-title] Rheumatology international
  • [ISO-abbreviation] Rheumatol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents, Non-Steroidal
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12. Shears E, Dehne K, Murata H, Abudu A, Grimer RJ, Tillman RM, Carter SR: Healing of ungrafted bone defects of the talus after benign tumour removal. Foot Ankle Surg; 2008;14(3):161-5
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  • [Title] Healing of ungrafted bone defects of the talus after benign tumour removal.
  • BACKGROUND: Curettage of benign tumours commonly results in significant bone defects that are reconstructed with autologous grafts, allografts, bone cement or bone substitute.
  • We have treated such defects in the talus without reconstruction with bone or any other material.
  • We now report the healing of these ungrafted defects in eight patients treated with curettage for benign talar tumours.
  • CONCLUSIONS: We conclude that bone grafting is not a necessary adjunct to the curettage of talar lesions.
  • [MeSH-major] Bone Neoplasms / surgery. Talus / surgery. Wound Healing
  • [MeSH-minor] Adolescent. Adult. Child. Chondroblastoma / surgery. Curettage. Female. Follow-Up Studies. Ganglion Cysts / surgery. Humans. Male. Osteoarthritis / etiology. Osteoblastoma / surgery. Postoperative Complications. Retrospective Studies. Young Adult

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  • (PMID = 19083636.001).
  • [ISSN] 1460-9584
  • [Journal-full-title] Foot and ankle surgery : official journal of the European Society of Foot and Ankle Surgeons
  • [ISO-abbreviation] Foot Ankle Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] France
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13. Svoboda M, Hamilton G, Thalhammer T: Steroid hormone metabolizing enzymes in benign and malignant human bone tumors. Expert Opin Drug Metab Toxicol; 2010 Apr;6(4):427-37
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  • [Title] Steroid hormone metabolizing enzymes in benign and malignant human bone tumors.
  • IMPORTANCE IN THE FIELD: Primary bone tumors are considered as (sex steroid) hormone-dependent tumors.
  • Osteosarcoma, osteoblastoma and bone cysts are preferentially found in males, while giant cell tumors are more common in females.
  • Indeed, bone tumor development and progression are influenced by sex steroid hormones derived from in situ synthesis in bone cells.
  • An overview is given and the expression and function of these enzymes in bone tumors are discussed.
  • TAKE HOME MESSAGE: Knowledge on pathways for the in situ formation of E2 in bone cells may allow the identification of potential targets for i) novel endocrine therapeutic options in primary bone tumors and ii) future preventive interventions.
  • [MeSH-major] Bone Neoplasms / enzymology. Bone Neoplasms / pathology. Bone and Bones / cytology. Bone and Bones / enzymology. Gonadal Steroid Hormones / metabolism

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  • (PMID = 20102288.001).
  • [ISSN] 1744-7607
  • [Journal-full-title] Expert opinion on drug metabolism & toxicology
  • [ISO-abbreviation] Expert Opin Drug Metab Toxicol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Gonadal Steroid Hormones; 4TI98Z838E / Estradiol
  • [Number-of-references] 89
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14. Lypka MA, Goos RR, Yamashita DD, Melrose R: Aggressive osteoblastoma of the mandible. Int J Oral Maxillofac Surg; 2008 Jul;37(7):675-8
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  • [Title] Aggressive osteoblastoma of the mandible.
  • We report a case of aggressive osteoblastoma of the mandible, an extremely rare primary bone tumor of the maxillofacial skeleton.
  • Although osteoblastomas are benign tumors requiring only curettage for cure, there is a small subset of tumors that exhibit locally aggressive behavior and have atypical histopathologic features.
  • The correct diagnosis must be based on clinical, radiographic and pathologic features.
  • [MeSH-major] Mandibular Neoplasms / diagnosis. Osteoblastoma / diagnosis
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Follow-Up Studies. Humans. Male. Radiography, Panoramic. Reconstructive Surgical Procedures. Tomography, X-Ray Computed

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  • (PMID = 18337062.001).
  • [ISSN] 0901-5027
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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15. Arkader A, Dormans JP: Osteoblastoma in the skeletally immature. J Pediatr Orthop; 2008 Jul-Aug;28(5):555-60
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  • [Title] Osteoblastoma in the skeletally immature.
  • BACKGROUND: Osteoblastoma is a rare benign and sometimes locally aggressive tumor with peak incidence in the second decade.
  • METHODS: The medical records and radiographs of all children diagnosed with osteoblastoma during a 17-year period were reviewed.
  • We recorded demographic information, time until diagnosis, location, clinical and radiographic characteristics, treatment, complications, and outcome at a minimum 2-year follow-up (range, 2-5 years).
  • There were 10 boys and 7 girls, with an average age at diagnosis of 11 years (range, 20 months-15 years).
  • The average time delay between onset of symptoms and diagnosis was 6.5 months (range, 2 months-2 years).
  • [MeSH-major] Bone Neoplasms / therapy. Osteoblastoma / therapy

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  • (PMID = 18580372.001).
  • [ISSN] 0271-6798
  • [Journal-full-title] Journal of pediatric orthopedics
  • [ISO-abbreviation] J Pediatr Orthop
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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16. Kaplan I, Nicolaou Z, Hatuel D, Calderon S: Solitary central osteoma of the jaws: a diagnostic dilemma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Sep;106(3):e22-9
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  • Osteomas are relatively rare benign osteogenic neoplasms, characterized by the proliferation of compact and/or cancellous bone.
  • Osteomas can develop as peripheral (periosteal) masses attached to the cortical plates or as central lesions arising from endosteal bone surfaces.
  • Whereas peripheral osteomas are fairly easy to diagnose, central osteomas pose a more challenging diagnostic problem and need to be differentiated from other similar lesions of the jaws, such as central ossifying fibroma, condensing osteitis, idiopathic osteosclerosis, osteoblastoma, cementoblastoma, and complex odontoma.
  • [MeSH-minor] Aged. Diagnosis, Differential. Female. Humans. Male. Middle Aged

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  • (PMID = 18602294.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 30
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17. Meli GA, Meli L, Chiaramonte R, Riva G, Pero G: Osteoblastoma of the orbit. A case report and review of the literature. Neuroradiol J; 2008 Feb 18;21(1):71-6
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  • [Title] Osteoblastoma of the orbit. A case report and review of the literature.
  • We describe a case of benign orbital tumour involving the frontal sinus and ethmoidal cells.
  • CT findings were typical of "bone tumour of the orbit", histological analysis yielded a diagnosis of benign osteoblastoma.
  • On MRI osteoblastoma shows an iso- low signal both in T1 and in T2 sequences.
  • The orbit is rarely involved by bone tumours, but all bone tumours may theoretically involve the orbit, often making it difficult to establish the right differential diagnosis by imaging.
  • For this reason we also examined the radiological signs of bone tumours involving other portions of the body.
  • Even though many literature reports suggest CT is the landmark in bone tumour diagnosis, we think it should always be accompanied by MRI.
  • MRI is known to overestimate local staging, but its contribution to differential diagnosis among various tumours may be decisive.

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  • (PMID = 24256752.001).
  • [ISSN] 1971-4009
  • [Journal-full-title] The neuroradiology journal
  • [ISO-abbreviation] Neuroradiol J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Liberman B, Gerniak A, Eshed I, Chechick A, Weiss I, Shabshin N: [Percutaneous CT guided radio-frequency ablation of osteoid osteoma and osteoblastoma]. Harefuah; 2010 Aug;149(8):494-7, 552
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  • [Title] [Percutaneous CT guided radio-frequency ablation of osteoid osteoma and osteoblastoma].
  • BACKGROUND: Osteoid osteoma (OO) is a benign osteoblastic bone lesion that causes severe local pain mainly at night, and usually responds to oral administration of NSAID.
  • Osteoblastoma is similar to OO in their histopathology features, but emerges frequently in the spine, and has a larger diameter than OO.
  • Percutaneous CT-guided radiofrequency ablation (RFA) is becoming the treatment of choice for osteoid osteoma and non-aggressive osteoblastoma in the last decade.
  • METHODS: During the period 2005-2009, 38 patients were diagnosed with osteoid osteoma (n = 34), and osteoblastoma (n = 4).
  • CONCLUSIONS: Percutaneous CT-guided radiofrequency ablation of osteoid osteoma and non-aggressive osteoblastoma is simple, safe, and reliable.
  • [MeSH-major] Bone Neoplasms / surgery. Catheter Ablation / methods. Osteoblastoma / surgery. Osteoma, Osteoid / surgery

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  • (PMID = 21341426.001).
  • [ISSN] 0017-7768
  • [Journal-full-title] Harefuah
  • [ISO-abbreviation] Harefuah
  • [Language] heb
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Israel
  • [Chemical-registry-number] 059QF0KO0R / Water
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19. Shintaku WH, Venturin JS, Langlais RP, Clark GT: Imaging modalities to access bony tumors and hyperplasic reactions of the temporomandibular joint. J Oral Maxillofac Surg; 2010 Aug;68(8):1911-21
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  • Benign and malignant tumors in the temporomandibular joint (TMJ) are rare.
  • The differential diagnosis for benign hyperplastic bony lesions in the TMJ should include condylar hyperplasia, osteochondroma, osteoma, chondroma, and osteoblastoma.
  • For the differential diagnosis, imaging is the most noninvasive method to evaluate the integrity of the TMJ.
  • To differentiate benign and malignant bony tumors, magnetic resonance imaging has a sensitivity and specificity of 44% and 95%, respectively.
  • [MeSH-major] Bone Neoplasms / diagnosis. Diagnostic Imaging / methods. Head and Neck Neoplasms / diagnosis. Temporomandibular Joint Disorders / diagnosis
  • [MeSH-minor] Cone-Beam Computed Tomography. Humans. Hyperplasia / diagnosis. Magnetic Resonance Imaging. Positron-Emission Tomography. Radiography, Panoramic. Sensitivity and Specificity. Temporomandibular Joint / pathology. Temporomandibular Joint / radiography. Temporomandibular Joint / radionuclide imaging. Tomography, Emission-Computed, Single-Photon. Tomography, X-Ray Computed


20. Santiago FR, Del Mar Castellano García M, Montes JL, García MR, Fernández JM: Treatment of bone tumours by radiofrequency thermal ablation. Curr Rev Musculoskelet Med; 2009 Mar;2(1):43-50
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  • [Title] Treatment of bone tumours by radiofrequency thermal ablation.
  • Other benign conditions (chondroblastoma, osteoblastoma, giant cell tumour, etc.) can also be treated by this technique, which is less invasive than traditional surgical procedures.
  • In other cases, it is combined with conventional therapies or other percutaneous treatments, e.g., cementoplasty, offering faster pain relief and bone strengthening.

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  • [Cites] AJNR Am J Neuroradiol. 2007 Apr;28(4):700-5 [17416824.001]
  • [Cites] J Vasc Interv Radiol. 2002 Oct;13(10):1047-50 [12397128.001]
  • [Cites] Skeletal Radiol. 2006 Jan;35(1):1-15 [16205922.001]
  • [Cites] Instr Course Lect. 2005;54:497-503 [15948474.001]
  • [Cites] J Vasc Interv Radiol. 2005 Jun;16(6):765-78 [15947040.001]
  • [Cites] Radiology. 2005 Jun;235(3):728-39 [15845798.001]
  • [Cites] J Clin Oncol. 1998 Mar;16(3):1218-25 [9508210.001]
  • [Cites] Cancer. 1997 Oct 15;80(8 Suppl):1628-45 [9362430.001]
  • [Cites] Orthop Clin North Am. 1996 Jul;27(3):559-74 [8649737.001]
  • [Cites] Skeletal Radiol. 1993 Oct;22(7):485-500 [8272884.001]
  • [Cites] Radiology. 1992 Apr;183(1):29-33 [1549690.001]
  • [Cites] J Clin Oncol. 1991 Mar;9(3):509-24 [1705581.001]
  • [Cites] Skeletal Radiol. 2002 Oct;31(10):597-602 [12324830.001]
  • [Cites] Pediatr Radiol. 2002 Aug;32(8):615-8 [12200642.001]
  • [Cites] Spine (Phila Pa 1976). 2002 Aug 1;27(15):E361-5 [12163737.001]
  • [Cites] Radiology. 2002 Jul;224(1):87-97 [12091666.001]
  • [Cites] Radiology. 2001 Nov;221(2):463-8 [11687691.001]
  • [Cites] J Vasc Interv Radiol. 2001 Sep;12(9):1021-32 [11535764.001]
  • [Cites] Skeletal Radiol. 2001 Apr;30(4):219-22 [11392296.001]
  • [Cites] J Bone Joint Surg Br. 2001 Apr;83(3):391-6 [11341426.001]
  • [Cites] Radiology. 2000 Dec;217(3):657-64 [11110925.001]
  • [Cites] J Bone Joint Surg Br. 2000 Nov;82(8):1125-8 [11132271.001]
  • [Cites] AJR Am J Roentgenol. 2000 Nov;175(5):1263-6 [11044019.001]
  • [Cites] AJR Am J Roentgenol. 2008 Jun;190(6):1492-4 [18492897.001]
  • [Cites] Eur Radiol. 2007 Nov;17(11):3012-3 [17622538.001]
  • [Cites] AJR Am J Roentgenol. 2007 Sep;189(3):W146-9 [17715082.001]
  • [Cites] Eur J Radiol. 2007 Jul;63(1):63-7 [17482405.001]
  • [Cites] CMAJ. 1986 Oct 15;135(8):895-9 [3756721.001]
  • [Cites] J Vasc Interv Radiol. 2004 Jul;15(7):707-12 [15231884.001]
  • [Cites] J Clin Oncol. 2004 Jan 15;22(2):300-6 [14722039.001]
  • [Cites] Radiology. 2003 Oct;229(1):171-5 [12944597.001]
  • [Cites] J Vasc Interv Radiol. 2003 Jun;14(6):773-7 [12817045.001]
  • [Cites] Arch Orthop Trauma Surg. 2003 Apr;123(2-3):86-90 [12721686.001]
  • [Cites] AJR Am J Roentgenol. 2003 Apr;180(4):1075-7 [12646458.001]
  • [Cites] AJR Am J Roentgenol. 2002 Dec;179(6):1633-42 [12438068.001]
  • [Cites] Eur Radiol. 2006 Apr;16(4):804-10 [16267666.001]
  • (PMID = 19468917.001).
  • [ISSN] 1935-973X
  • [Journal-full-title] Current reviews in musculoskeletal medicine
  • [ISO-abbreviation] Curr Rev Musculoskelet Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2684952
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21. Tamiolakis D, Thomaidis V, Tsamis I, Alexiadis G, Seretis K: Clinical, radiological and histological correlation in the diagnostic work-up of cemento-ossifying fibroma of the maxilla: case report. Chirurgia (Bucur); 2007 May-Jun;102(3):359-62
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  • This lesion appears within the bone although in some occasions it involves the gingivae soft tissues.
  • It is a slow growing and well-defined tumorous lesion, because of this, it is considered as a benign lesion.
  • The histology was that of a benign fibro-osseous proliferation composed of bony spicules and spherules admixed with a fibrous stroma.
  • Clinical and radiological information was essential for the final diagnosis.
  • The histologic findings alone may be similar to other pathologies such as osteoblastoma, low-grade osteosarcoma and particularly to fibrous dysplasia.
  • An accurate diagnosis requires careful clinical, radiological and histological correlation in order to make an optimal treatment and an excellent outcome.
  • [MeSH-major] Fibroma, Ossifying / diagnosis. Maxillary Neoplasms / diagnosis

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  • (PMID = 17687869.001).
  • [ISSN] 1221-9118
  • [Journal-full-title] Chirurgia (Bucharest, Romania : 1990)
  • [ISO-abbreviation] Chirurgia (Bucur)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Romania
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22. Li GD, Cai ZD, Zhang YQ, Gong HY, Tang H, Zhang QL: [Gene profiling of MAPK pathway in human osteosarcoma]. Zhonghua Zhong Liu Za Zhi; 2009 May;31(5):340-5
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  • Immunohistochemical technique was used to detect the expressions of ERK1/2, JNK and p38 proteins among 48 osteosarcoma and benign 24 osteoblastic tumor samples.
  • [MeSH-major] Bone Neoplasms / genetics. Gene Expression Profiling. Mitogen-Activated Protein Kinases / metabolism. Osteosarcoma / genetics. Signal Transduction
  • [MeSH-minor] Adolescent. Adult. Aged. Cell Line, Tumor. Child. Female. Humans. JNK Mitogen-Activated Protein Kinases / metabolism. Male. Middle Aged. Mitogen-Activated Protein Kinase 1 / metabolism. Mitogen-Activated Protein Kinase 3 / metabolism. Oligonucleotide Array Sequence Analysis. Osteoblastoma / genetics. Osteoblastoma / metabolism. Osteoblastoma / pathology. Young Adult. p38 Mitogen-Activated Protein Kinases / metabolism


23. Mir NA, Baba AN, Maajid S, Badoo AR, Mir GR: Osteoblastoma of body of the talus--Report of a rare case with atypical radiological features. Foot Ankle Surg; 2010 Jun;16(2):e24-6
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  • [Title] Osteoblastoma of body of the talus--Report of a rare case with atypical radiological features.
  • Osteoblastoma is a benign bone tumour found commonly in the spine and long tubular bones.
  • Osteoblastoma of the body of talus is a very rare entity.
  • Analysis of clinical, radiological and histological findings confirmed the diagnosis of osteoblastoma.
  • The case is reported for the rarity of the site and atypical radiological features that osteoblastoma can present with.
  • [MeSH-major] Bone Neoplasms / radiography. Osteoblastoma / radiography. Rare Diseases. Talus. Tomography, X-Ray Computed
  • [MeSH-minor] Adolescent. Diagnosis, Differential. Follow-Up Studies. Humans. Male. Osteotomy / methods

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  • [Copyright] Copyright 2009 European Foot and Ankle Society. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20483122.001).
  • [ISSN] 1460-9584
  • [Journal-full-title] Foot and ankle surgery : official journal of the European Society of Foot and Ankle Surgeons
  • [ISO-abbreviation] Foot Ankle Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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24. Martel Villagrán J, Bueno Horcajadas A, Ortiz Cruz EJ: [Percutaneous radiofrequency ablation of benign bone tumors: osteoid osteoma, osteoblastoma, and chondroblastoma]. Radiologia; 2009 Nov-Dec;51(6):549-58
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  • [Title] [Percutaneous radiofrequency ablation of benign bone tumors: osteoid osteoma, osteoblastoma, and chondroblastoma].
  • [Transliterated title] Tratamiento mediante radiofrecuencia percutánea de los tumores óseos benignos: osteoma osteoide, osteoblastoma y condroblastoma.
  • We report our experience in the computed tomography (CT)-guided percutaneous radiofrequency ablation of more than 100 benign bone tumors in the last eight years.
  • We affirm that this should be the technique of choice in the vast majority of osteoid osteomas; it can also be applied as a definitive treatment in many cases of osteoblastomas or chondroblastomas as well as in less common benign bone tumors.
  • [MeSH-major] Bone Neoplasms / surgery. Catheter Ablation. Chondroblastoma / surgery. Osteoblastoma / surgery. Osteoma, Osteoid / surgery

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  • (PMID = 19863982.001).
  • [ISSN] 0033-8338
  • [Journal-full-title] Radiología
  • [ISO-abbreviation] Radiologia
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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25. Blackwell JB, Curnow MN: Benign bone tumours in Western Australia, 1972-1996. Pathology; 2007 Dec;39(6):567-74
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  • [Title] Benign bone tumours in Western Australia, 1972-1996.
  • AIMS: To review the benign bone tumours accessioned by the Bone Tumour Registry (BTR) of Western Australia (WA) during the years 1972-1996 and to determine the incidence of the more common types.
  • RESULTS: During the 25 year period, 849 benign tumours were accessioned and incidence rates have been calculated for 86 chondromas, 68 osteoid osteomas, 47 giant cell tumours, 32 chondroblastomas, 15 periosteal chondromas and 13 chondromyxoid fibromas.
  • CONCLUSION: The BTR provides a valuable resource for the study of primary bone tumours.
  • This review has established reliable incidence rates for the six most common benign tumours.
  • Such information is rarely available for benign tumours.
  • It has also disclosed that osteoblastoma is only four times less frequent than osteosarcoma, which is five times higher than published figures from North America.
  • [MeSH-major] Bone Neoplasms / pathology. Registries

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  • (PMID = 18027260.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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26. Karantanas A, Dailiana Z, Malizos K: The role of MR imaging in scaphoid disorders. Eur Radiol; 2007 Nov;17(11):2860-71
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  • The scaphoid bone of the wrist is one of the most commonly fractured bones in the body.
  • In patients with normal initial plain radiographs, MR imaging can discriminate occult fractures from bone bruises and may also demonstrate ligamentous disruption.
  • The non-traumatic disorders of the scaphoid include post-traumatic osteoarthritis, inflammatory bone marrow edema in patients with rheumatoid arthritis, and osteomyelitis.
  • MR imaging is helpful in all the above disorders to demonstrate early bone marrow edema, cartilage degeneration and associated subchondral marrow changes.
  • The most commonly found tumors in the scaphoid are usually benign and include enchondroma, osteoblastoma and osteoid osteoma.
  • MR imaging is not mandatory for the initial diagnosis, which should be based on plain X-ray findings.
  • [MeSH-major] Magnetic Resonance Imaging / methods. Musculoskeletal Diseases / diagnosis. Musculoskeletal Diseases / diagnostic imaging. Scaphoid Bone / diagnostic imaging. Scaphoid Bone / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Biomechanical Phenomena / methods. Bone and Bones / metabolism. Female. Fracture Healing. Humans. Male. Middle Aged. Osteonecrosis. Radionuclide Imaging / methods. Time Factors. Tomography, X-Ray Computed / methods

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  • [Cites] J Bone Joint Surg Br. 2002 Mar;84(2):273-4 [11922372.001]
  • [Cites] J Hand Surg Br. 1992 Dec;17 (6):697-700 [1484258.001]
  • [Cites] Skeletal Radiol. 2005 Jun;34(6):314-20 [15834565.001]
  • [Cites] Br J Radiol. 2003 May;76(905):296-300 [12763944.001]
  • [Cites] J Hand Surg Am. 1985 Sep;10(5):597-605 [3900189.001]
  • [Cites] Rev Chir Orthop Reparatrice Appar Mot. 1999 Sep;85(5):503-6 [10507113.001]
  • [Cites] J Trauma. 2004 Oct;57(4):851-4 [15514541.001]
  • [Cites] J Trauma. 2005 Jan;58(1):76-82 [15674154.001]
  • [Cites] Acta Orthop Scand. 1998 Jun;69(3):291-4 [9703406.001]
  • [Cites] J Trauma. 1996 Jul;41(1):73-6 [8676426.001]
  • [Cites] Radiology. 2003 Jun;227(3):701-7 [12773676.001]
  • [Cites] J Am Acad Orthop Surg. 2002 Jan-Feb;10(1):32-42 [11809049.001]
  • [Cites] Arch Orthop Trauma Surg. 1996;115(1):1-4 [8775701.001]
  • [Cites] J Bone Joint Surg Br. 2004 Jul;86(5):705-13 [15274268.001]
  • [Cites] Radiology. 2005 Dec;237(3):1008-13 [16304116.001]
  • [Cites] Eur J Radiol. 2004 Jun;50(3):217-24 [15145480.001]
  • [Cites] J Hand Surg Am. 2003 Sep;28(5):767-78 [14507506.001]
  • [Cites] J Hand Surg Br. 2001 Aug;26(4):330-4 [11469835.001]
  • [Cites] Saudi Med J. 2002 Aug;23(8):1005-7 [12235480.001]
  • [Cites] AJR Am J Roentgenol. 2001 Dec;177(6):1257-63 [11717059.001]
  • [Cites] Orthopedics. 1992 Jun;15(6):739-41 [1608867.001]
  • [Cites] Radiology. 1993 Dec;189(3):901-4 [8234723.001]
  • [Cites] J Hand Surg Br. 1995 Dec;20(6):726-35 [8770730.001]
  • [Cites] J Orthop Sci. 2005;10(1):99-102 [15666131.001]
  • [Cites] Radiology. 1997 Apr;203(1):245-50 [9122402.001]
  • [Cites] J Hand Surg Am. 1999 Jul;24(4):761-76 [10447168.001]
  • [Cites] J Hand Surg Br. 2002 Apr;27(2):165-70 [12027494.001]
  • [Cites] J Hand Surg Br. 1998 Dec;23 (6):817-9 [9888693.001]
  • [Cites] J Bone Joint Surg Br. 1988 Mar;70(2):299-301 [3346310.001]
  • [Cites] AJR Am J Roentgenol. 2002 May;178(5):1239-45 [11959740.001]
  • [Cites] Am J Orthop (Belle Mead NJ). 2006 Jul;35(7):329-32 [16927659.001]
  • [Cites] Radiology. 2001 Apr;219(1):11-28 [11274530.001]
  • [Cites] Eur Radiol. 2000;10(12):1926-8 [11305572.001]
  • [Cites] Genet Couns. 2005;16(4):413-5 [16440885.001]
  • [Cites] Clin Orthop Relat Res. 1997 Mar;(336):240-6 [9060510.001]
  • [Cites] J Bone Joint Surg Br. 1999 Jan;81(1):85-90 [10068010.001]
  • [Cites] J Hand Surg Br. 1994 Aug;19(4):498-504 [7964103.001]
  • [Cites] AJR Am J Roentgenol. 2000 Jan;174(1):141-9 [10628470.001]
  • [Cites] J Hand Surg Br. 2004 Oct;29(5):444-8 [15336746.001]
  • [Cites] J Bone Joint Surg Br. 2001 Aug;83(6):809-14 [11521919.001]
  • [Cites] Orthop Clin North Am. 1990 Jul;21(3):515-43 [2367104.001]
  • [Cites] J Hand Surg Am. 1989 Sep;14 (5):781-90 [2794392.001]
  • [Cites] J Comput Assist Tomogr. 1997 Jul-Aug;21(4):511-5 [9216753.001]
  • [Cites] Clin Orthop Relat Res. 1986 Jan;(202):57-67 [3955970.001]
  • [Cites] Clin Radiol. 2005 Oct;60(10 ):1106-10 [16179171.001]
  • [Cites] AJR Am J Roentgenol. 1997 May;168(5):1287-93 [9129428.001]
  • [Cites] J Hand Surg Br. 1996 Aug;21(4):496-500 [8856542.001]
  • [Cites] Clin Radiol. 2005 Jun;60(6):627-36 [16038689.001]
  • [Cites] Hand Clin. 2001 Nov;17(4):525-32 [11775465.001]
  • [Cites] J Hand Surg Br. 1992 Feb;17(1):20-7 [1640140.001]
  • [Cites] Aust N Z J Surg. 1983 Apr;53(2):133-7 [6576759.001]
  • [Cites] J Bone Joint Surg Am. 1985 Mar;67(3):428-32 [3972868.001]
  • [Cites] J Trauma. 1997 Feb;42(2):247-53 [9042876.001]
  • [Cites] Australas Radiol. 1998 Feb;42(1):10-5 [9509596.001]
  • [Cites] AJR Am J Roentgenol. 1997 Mar;168(3):779-86 [9057534.001]
  • [Cites] N Z Med J. 2005 Feb 11;118(1209):U1296 [15711629.001]
  • [Cites] J Hand Surg Br. 1995 Apr;20(2):201-5 [7797970.001]
  • [Cites] Radiology. 1988 Apr;167(1):167-72 [3162326.001]
  • [Cites] J Hand Surg Am. 1991 May;16(3):479-84 [1861031.001]
  • [Cites] Ann Rheum Dis. 1998 Jun;57(6):350-6 [9771209.001]
  • [Cites] J Hand Surg Am. 2005 Nov;30(6):1156-60 [16344171.001]
  • [Cites] J Hand Surg Am. 1998 Mar;23 (2):334-7 [9556278.001]
  • [Cites] AJR Am J Roentgenol. 2005 May;184(5):1470-4 [15855098.001]
  • [Cites] Skeletal Radiol. 1998 Dec;27(12 ):683-7 [9921930.001]
  • [Cites] J Hand Surg Am. 1990 Jul;15(4):557-64 [2380517.001]
  • [Cites] Ann Rheum Dis. 2001 Sep;60(9):859-68 [11502613.001]
  • [Cites] Arch Orthop Trauma Surg. 2002 Jul;122(6):369-70 [12136305.001]
  • [Cites] J Hand Surg Br. 1992 Jun;17(3):289-310 [1624863.001]
  • [Cites] Orthop Clin North Am. 1992 Jan;23(1):7-17 [1729671.001]
  • [Cites] Magn Reson Imaging. 1990;8(4):357-61 [2392023.001]
  • (PMID = 17351778.001).
  • [ISSN] 0938-7994
  • [Journal-full-title] European radiology
  • [ISO-abbreviation] Eur Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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27. Dabholkar JP, Vora K, Vaidya A, Sharma A: Benign jaw tumors. Indian J Otolaryngol Head Neck Surg; 2009 Sep;61(3):240-4
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  • [Title] Benign jaw tumors.
  • They are usually benign in nature and can affect the functions of mastication, swallowing and cause facial deformity.
  • They make about 3% of all bone tumors with a tendency for a local recurrence if a wide excision is not contemplated at the first attempt.

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  • [Cites] Folia Med Cracov. 1998;39(1-2):35-141 [10481376.001]
  • [Cites] Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005 Feb;99(2):191-5 [15660091.001]
  • [Cites] Br J Oral Maxillofac Surg. 2006 Oct;44(5):386-8 [16182417.001]
  • (PMID = 23120644.001).
  • [ISSN] 2231-3796
  • [Journal-full-title] Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
  • [ISO-abbreviation] Indian J Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3449977
  • [Keywords] NOTNLM ; Ameloblastoma / Dentigerous cyst / Jaw tumors / Odontomes / Osteoblastoma
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28. Sang H, Wang Z, Guo Z, Wang L, Li J, Meng G, Li X, Lu J: [Clinical results and the mechanism of bone healing for the repair of bone defects due to tumor resection with novel interporous TCP]. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2008 Apr;22(4):463-7
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  • [Title] [Clinical results and the mechanism of bone healing for the repair of bone defects due to tumor resection with novel interporous TCP].
  • OBJECTIVE: To investigate the clinical results and the mechanism of bone healing for the repair of bone defects following tumor resection with novel interporous TCP bone graft, and to test the hypothesis of "structural transplantation".
  • METHODS: From January 2003 to December 2005, 61 cases of various bone defects following the curettage of the benign bone tumors were treated with interporous TCP, with 33 males and 28 females, including bone fibrous dysplasia in 8 cases, bone cyst in 23 cases, eosinophilic granuloma in 12 cases, enchondroma in 13 cases, non-ossifying fibroma in 2 cases, and osteoblastoma in 3 cases.
  • They all had good wound healing and bone regeneration.
  • The bone defects were repaired gradually from 1 to 6 months after operation (bone healing at average 2.6 months after surgery) with a bone healing rate up to 96.7%.
  • Given revision operation, this case gained bone healing.
  • Radiographically, the interface between the implanted bone and host bone became fuzzy 1 month after implantation, indicating the beginning of new bone formation.
  • Three months later, the absorption of the interporous TCP was noticed from peripheral to the center of the implanted bone evidenced by the vague or fuzzy realm.
  • New bone formation could be seen both in peripheral and central areas.
  • Six months later, implanted bone and host bone merged together and the bone defect was totally repaired, with 78.9% degradation rate of the implanted TCP.
  • Twelve months later, the majority of the implanted bone was absorbed and bone remodeling was established.
  • In the cases that were followed up for 24 months, the function of affected extremity was excellent with good bone remodeling without recurrence.
  • Pathologically, the interporous TCP closely contacted the host bone inside the humerus 1 month after grafting.
  • The interface between the implanted bone and host bone became fuzzy, and vascularized tissue began growing inside the implanted graft as a "lining" structure.
  • CONCLUSION: The interporous TCP proves to be effective for clinical reparation of bone defects following tumor resection.
  • The inside three-dimensional porous structure simulates the natural bionic bone structure which is suitable for recruitment related cells in-growth into the scaffold, colonizing and proliferation companied with the process of vascularize, finally with the new bone formation.
  • The novel interporous TCP may boast both bone conductive and bone inductive activities, as an appealing "structural transplantation" bone graft.
  • [MeSH-major] Bone Diseases / surgery. Bone Neoplasms / surgery. Bone Substitutes. Calcium Phosphates. Prostheses and Implants. Wound Healing
  • [MeSH-minor] Adolescent. Adult. Biocompatible Materials. Bone Regeneration / physiology. Bone Transplantation. Child. Child, Preschool. Female. Follow-Up Studies. Humans. Infant. Male. Middle Aged. Reconstructive Surgical Procedures. Treatment Outcome

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  • (PMID = 18575450.001).
  • [ISSN] 1002-1892
  • [Journal-full-title] Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery
  • [ISO-abbreviation] Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Biocompatible Materials; 0 / Bone Substitutes; 0 / Calcium Phosphates
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29. Oommen AT, Madhuri V, Walter NM: Benign tumors and tumor-like lesions of the calcaneum: a study of 12 cases. Indian J Cancer; 2009 Jul-Sep;46(3):234-6
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  • [Title] Benign tumors and tumor-like lesions of the calcaneum: a study of 12 cases.
  • Benign tumors of the calcaneum are rare.
  • Cystic lesions such as simple bone cysts and aneurysmal bone cysts are commonly seen.
  • MATERIALS AND METHODS: We analyzed noninfectious, noninflammatory, benign lesions of the calcaneum seen in the Orthopedic Out Patient Department from 1991 to 2003.
  • RESULTS: Twelve benign lesions were seen in 12 patients.
  • In our series, cysts predominated, with three aneurysmal bone cysts and five simple bone cysts.
  • The other benign tumors were: one fibrous dysplasia, one vascular hamartoma, one osteoblastoma, and one chondromyxoid fibroma.
  • The bone cysts were treated by curettage, with or without bone grafting, except for one large aneurysmal bone cyst, which was treated by excision of the calcaneum.
  • CONCLUSION: The calcaneum is an uncommon site for most bone tumors, and in our series, bone cysts were the most common benign lesions.
  • Curettage and bone grafting or the use of bone substitutes can be effectively used in the treatment of symptomatic bone cysts of the calcaneum.
  • [MeSH-major] Bone Cysts / pathology. Bone Cysts, Aneurysmal / pathology. Bone Neoplasms / pathology. Calcaneus / pathology. Osteoblastoma / pathology

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  • (PMID = 19574677.001).
  • [ISSN] 0019-509X
  • [Journal-full-title] Indian journal of cancer
  • [ISO-abbreviation] Indian J Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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30. Park YK, Kim EJ, Kim SW: Osteoblastoma of the ethmoid sinus. Skeletal Radiol; 2007 May;36(5):463-7
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  • [Title] Osteoblastoma of the ethmoid sinus.
  • An osteoblastoma is a benign bone tumor that most often occurs in the vertebral column and the long bones of the extremities.
  • We report an osteoblastoma of the ethmoid sinus in a 13-year-old boy who presented with exophthalmos.
  • A mixture of ground glass opacity and dense bone was present.
  • Histologically, the lesion was composed of proliferating osteoblasts along with small trabeculae of woven bone and rich vascular fibrous stroma.
  • The literature concerning occurrence of osteoblastoma in this unusual location is reviewed and discussed.
  • [MeSH-major] Ethmoid Sinus / pathology. Ethmoid Sinus / surgery. Osteoblastoma / diagnosis. Osteoblastoma / surgery. Paranasal Sinus Neoplasms / diagnosis. Paranasal Sinus Neoplasms / surgery

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  • [Cites] Arch Otolaryngol. 1979 Oct;105(10 ):623-5 [485933.001]
  • [Cites] An Esp Pediatr. 1997 Jan;46(1):83-4 [9082899.001]
  • [Cites] J Clin Pathol. 1993 Nov;46(11):1024-9 [8254089.001]
  • [Cites] Ann Laringol Otol Rinol Faringol. 1965;64(6):768-77 [5218396.001]
  • [Cites] J Comput Tomogr. 1985 Oct;9(4):347-50 [4053663.001]
  • [Cites] Laryngorhinootologie. 1991 May;70(5):275-7 [2064707.001]
  • [Cites] Klin Oczna. 1975 Mar;45(3):247-51 [1117656.001]
  • [Cites] Otolaryngol Pol. 2004;58(3):649-52 [15311621.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 1996 Dec 5;38(1):89-95 [9119598.001]
  • [Cites] Am J Clin Pathol. 1975 Mar;63(3):391-6 [1115044.001]
  • [Cites] Rhinology. 1983 Dec;21(4):373-5 [6665425.001]
  • [Cites] Cancer. 1974 May;33(5):1289-305 [4207295.001]
  • [Cites] Otolaryngol Pol. 1974;28(5):575-9 [4419075.001]
  • [Cites] J Neurosurg. 1997 Oct;87(4):625-8 [9322852.001]
  • [Cites] Cancer. 1985 Jan 15;55(2):416-26 [3855268.001]
  • [Cites] Otolaryngol Head Neck Surg. 1980 Jul-Aug;88(4):397-402 [6821422.001]
  • [Cites] J Laryngol Otol. 1993 Aug;107(8):737-9 [8409731.001]
  • [Cites] Skeletal Radiol. 2002 Mar;31(3):179-82 [11935205.001]
  • [Cites] J Laryngol Otol. 1978 Apr;92(4):337-45 [641417.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Ann Otolaryngol Chir Cervicofac. 1976 Oct-Nov;93(10-11):661-8 [1027351.001]
  • [Cites] Virchows Arch A Pathol Anat Histopathol. 1985;408(2-3):297-305 [3936268.001]
  • [Cites] AJR Am J Roentgenol. 2004 May;182(5):1343-4 [15868703.001]
  • [Cites] J Laryngol Otol. 1997 Sep;111(9):865-8 [9373556.001]
  • [Cites] Ann Pathol. 1985;5(2):131-6 [4041187.001]
  • [Cites] Head Neck Surg. 1983 Sep-Oct;6(1):605-9 [6629798.001]
  • [Cites] J Laryngol Otol. 1986 Feb;100(2):229-32 [3950490.001]
  • (PMID = 17265159.001).
  • [ISSN] 0364-2348
  • [Journal-full-title] Skeletal radiology
  • [ISO-abbreviation] Skeletal Radiol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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31. Lucas DR: Osteoblastoma. Arch Pathol Lab Med; 2010 Oct;134(10):1460-6
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  • [Title] Osteoblastoma.
  • Osteoblastoma is a rare benign bone tumor.
  • Although the histologic features in most cases are distinctive, there are various permutations that make the diagnosis challenging.
  • It can mimic a variety of other benign bone tumors, but more importantly, distinguishing it from osteoblastoma-like osteosarcoma can be difficult.
  • In this case report, I describe the clinicopathologic findings for a 13-year-old adolescent boy with T7 spinal osteoblastoma and review salient clinical, radiographic, and pathologic features of osteoblastoma, as well as the differential diagnoses.
  • [MeSH-major] Bone Neoplasms / pathology. Osteoblastoma / pathology. Spinal Neoplasms / pathology
  • [MeSH-minor] Adolescent. Cartilage, Articular / pathology. Cartilage, Articular / radiography. Diagnosis, Differential. Humans. Male. Osteoblasts / pathology. Osteoblasts / radiography. Osteoclasts / pathology. Osteoclasts / radiography. Tomography, X-Ray Computed

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  • (PMID = 20923301.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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32. James SL, Panicek DM, Davies AM: Bone marrow oedema associated with benign and malignant bone tumours. Eur J Radiol; 2008 Jul;67(1):11-21
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  • [Title] Bone marrow oedema associated with benign and malignant bone tumours.
  • Bone marrow oedema is associated with a wide variety of pathological processes including both benign and malignant bone tumours.
  • This imaging finding in relation to intraosseous tumours can aid in providing a more focused differential diagnosis.
  • In this review, we will discuss the MR imaging of bone marrow oedema surrounding intraosseous neoplasms.
  • Benign lesions commonly associated with bone marrow oedema include osteoid osteoma, osteoblastoma, chondroblastoma and Langerhan's cell histiocytosis.
  • Metastases and malignant primary bone tumours such as osteosarcoma, Ewing's sarcoma and chondrosarcoma may also be surrounded by bone marrow oedema.
  • Finally, the importance of bone marrow oedema in assessment of post chemotherapeutic response is addressed.
  • [MeSH-major] Bone Marrow Diseases / complications. Bone Marrow Diseases / diagnosis. Bone Neoplasms / complications. Bone Neoplasms / diagnosis. Diagnostic Imaging / methods. Edema / complications. Edema / diagnosis
  • [MeSH-minor] Diagnosis, Differential. Humans


33. Giannico G, Holt GE, Homlar KC, Johnson J, Pinnt J, Bridge JA: Osteoblastoma characterized by a three-way translocation: report of a case and review of the literature. Cancer Genet Cytogenet; 2009 Dec;195(2):168-71
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  • [Title] Osteoblastoma characterized by a three-way translocation: report of a case and review of the literature.
  • Osteoblastoma, an uncommon primary bone tumor, produces both osteoid and primitive woven bone in a background of fibrovascular connective tissue.
  • Although most osteoblastomas are considered benign, a controversial aggressive variant has been described, which may cause diagnostic confusion with malignant tumors such as osteosarcoma.
  • To date, no specific diagnostic cytogenetic or molecular marker has been identified for osteoblastoma to aid in its distinction.
  • Conventional cytogenetic analysis of an osteoblastoma arising in the femur of a 23-year-old woman revealed a novel three-way translocation involving chromosomes 1, 2 and 14 [t(1;2;14) (q42;q13;q24)].
  • [MeSH-major] Bone Neoplasms / genetics. Osteoblastoma / genetics. Translocation, Genetic

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  • (PMID = 19963118.001).
  • [ISSN] 1873-4456
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 20
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34. Lee YG, Cho CW: Benign osteoblastoma located in the parietal bone. J Korean Neurosurg Soc; 2010 Aug;48(2):170-2
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  • [Title] Benign osteoblastoma located in the parietal bone.
  • Benign osteoblastoma is an uncommon primary bone tumor, extremely rare in calvarium.
  • We present a case of a 25-year-old female with an osteoblastoma of parietal bone which was totally resected.
  • The authors discussed the clinical presentation, radiographic finding, differential diagnosis and management of the benign calvarial osteoblastoma with a review of the literature.

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  • (PMID = 20856669.001).
  • [ISSN] 1598-7876
  • [Journal-full-title] Journal of Korean Neurosurgical Society
  • [ISO-abbreviation] J Korean Neurosurg Soc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2941863
  • [Keywords] NOTNLM ; Osteoblastoma / Parietal bone
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35. Yang JZ, Zhang XH, Liu JR, Ding Y, Gao F, Wang Y: [Expression and significance of N-cadherin and β-catenin protein in osteosarcoma]. Zhonghua Zhong Liu Za Zhi; 2010 Aug;32(8):586-9
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  • METHODS: The expressions of N-cadherin and β-catenin at protein level were detected by immunohistochemical staining in 54 cases of osteosarcoma, 11 cases of osteoid osteoma, 7 cases of osteoblastoma and 8 cases of newly formed bone in nonmalignant bone diseases.
  • RESULTS: In newly formed bone, osteoblastoma, osteoid osteoma and osteosarcoma, the positive expression rate of N-cadherin protein was 75.0%, 71.4%, 63.6% and 35.2%, respectively.
  • The positive expression rate of N-cadherin protein in osteosarcoma was significantly lower than that in osteoid osteoma, osteoblastoma and newly formed bone in nonmalignant bone diseases (P = 0.035).
  • In newly formed bone, osteoblastoma, osteoid osteoma and osteosarcoma, the aberrant expression rate of β-catenin protein was 12.5%, 28.6%, 27.3% and 66.7%, respectively.
  • The aberrant expression rate of β-catenin protein in osteosarcoma was significantly higher than that in osteoid osteoma, osteoblastoma and newly formed bone (P = 0.002).
  • [MeSH-major] Bone Neoplasms / metabolism. Cadherins / metabolism. Lung Neoplasms / metabolism. Osteosarcoma / metabolism. beta Catenin / metabolism
  • [MeSH-minor] Adolescent. Adult. Child. Female. Follow-Up Studies. Humans. Male. Middle Aged. Osteoblastoma / metabolism. Osteoma, Osteoid / metabolism. Survival Rate. Young Adult


36. Wootton-Gorges SL: MR imaging of primary bone tumors and tumor-like conditions in children. Magn Reson Imaging Clin N Am; 2009 Aug;17(3):469-87, vi
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  • [Title] MR imaging of primary bone tumors and tumor-like conditions in children.
  • This article provides a review of the MR imaging features of the major primary malignant and benign bone tumors and tumorlike conditions encountered in the pediatric population.
  • Benign lesions discussed include simple bone cysts, aneurysmal bone cysts, giant cell tumor, osteochondroma, enchondroma, chondroblastoma, osteoid osteoma, osteoblastoma, nonossifying fibroma, fibrous dysplasia, osteofibrous dysplasia, hemangioma, and histiocytosis.
  • The use of MR imaging in the diagnosis of these lesions is discussed, and the text is enhanced with imaging examples of the lesions.
  • [MeSH-major] Bone Neoplasms / diagnosis. Magnetic Resonance Imaging / methods
  • [MeSH-minor] Adolescent. Bone Cysts / diagnosis. Bone Cysts / pathology. Cartilage Diseases / diagnosis. Cartilage Diseases / pathology. Child. Contrast Media. Humans

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  • (PMID = 19524197.001).
  • [ISSN] 1557-9786
  • [Journal-full-title] Magnetic resonance imaging clinics of North America
  • [ISO-abbreviation] Magn Reson Imaging Clin N Am
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media
  • [Number-of-references] 44
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37. Roessner A: [Bone tumors]. Verh Dtsch Ges Pathol; 2007;91:83-6
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  • [Title] [Bone tumors].
  • The primary round cell tumors of the skeletal system focus on the differential diagnosis of Ewing sarcoma.
  • Therefore, in most cases, the differential diagnosis to other "round cell" tumors of the skeletal system no longer causes great problems.
  • Besides the differential diagnosis of chondrogenic tumors, the diagnosis of osteoid-forming tumors is very problematic histologically.
  • Focus of attention is the diagnosis of highly malignant osteosarcoma.
  • This must be differentiated from the low malignant, intramedullary osteosarcomas, as well as from benign, osteoid-forming tumors and -like tumors.
  • Especially the tumors located at the border between highly malignant osteosarcoma and benign osteoblastoma are difficult as far as the differential diagnosis is concerned.
  • [MeSH-major] Bone Neoplasms / pathology
  • [MeSH-minor] Diagnosis, Differential. Fibrous Dysplasia of Bone / pathology. Humans. Translocation, Genetic

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  • (PMID = 18314599.001).
  • [ISSN] 0070-4113
  • [Journal-full-title] Verhandlungen der Deutschen Gesellschaft für Pathologie
  • [ISO-abbreviation] Verh Dtsch Ges Pathol
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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38. Arantes M, Resende M, Honavar M, Pires MM, Pereira JR, Vaz AR: Benign osteoblastoma of the sphenoid bone. Skull Base; 2009 Nov;19(6):437-41
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  • [Title] Benign osteoblastoma of the sphenoid bone.
  • Osteoblastoma is an uncommon benign bone tumor that accounts for 1% of all primary bone tumors.
  • Well documented in the spine and long bones, it is rarely found in the skull, namely in the sphenoid bone, with only five cases reported in the literature.
  • We report a case of an 11-year-old girl with a histologically confirmed benign osteoblastoma in an unusual location and an atypical aspect on the imaging studies.

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  • [Cites] Cancer. 1956 Sep-Oct;9(5):1044-52 [13364889.001]
  • (PMID = 20436846.001).
  • [ISSN] 1532-0065
  • [Journal-full-title] Skull base : official journal of North American Skull Base Society ... [et al.]
  • [ISO-abbreviation] Skull Base
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2793891
  • [Keywords] NOTNLM ; Benign osteoblastoma / child / radical resection / sphenoid bone
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39. Villalobos CE, Rybak LD, Steiner GC, Wittig JC: Osteoblastoma of the sternum--case report and review of the literature. Bull NYU Hosp Jt Dis; 2010;68(1):55-9
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  • [Title] Osteoblastoma of the sternum--case report and review of the literature.
  • Osteoblastoma is an extremely rare entity that represents less than 1% of all bone tumors, and affects twice as many males as females with peak incidence between 15 and 20 years.
  • Osteoblastoma does not have a classic presentation, but can vary with the location and size of the tumor.
  • Osteoblastoma is a benign tumor with an aggressive behavior.
  • The treatment is wide surgical resection, otherwise it continues to enlarge and destroy the bone and surrounding structures.
  • We report a 32-year-old male with an osteoblastoma of this sternum who was treated with an en-bloc resection and reconstruction with Marlex((R)) and a methylmethacrylate plate.
  • [MeSH-major] Bone Neoplasms / surgery. Orthopedic Procedures. Osteoblastoma / surgery. Sternum / surgery
  • [MeSH-minor] Adult. Biopsy. Bone Plates. Humans. Magnetic Resonance Imaging. Male. Methylmethacrylate. Polypropylenes. Prosthesis Design. Surgical Mesh. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 20345366.001).
  • [ISSN] 1936-9727
  • [Journal-full-title] Bulletin of the NYU hospital for joint diseases
  • [ISO-abbreviation] Bull NYU Hosp Jt Dis
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Polypropylenes; 196OC77688 / Methylmethacrylate
  • [Number-of-references] 22
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40. Bhagat S, Sharma H, Bansal M, Reid R: Presentation and outcome of primary tumors of the patella. J Knee Surg; 2008 Jul;21(3):212-6
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  • One patient with chondroblastoma underwent curettage only; the second patient underwent curettage and bone grafting.
  • Patients with osteoblastoma and osteitis fibrosa cystica underwent excision of the lesion.
  • A satisfactory outcome can be expected in the majority because of the predominantly benign nature of the lesions and straightforward operative intervention after diagnosis.
  • [MeSH-major] Bone Neoplasms / diagnosis. Bone Neoplasms / surgery. Patella

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  • (PMID = 18686483.001).
  • [ISSN] 1538-8506
  • [Journal-full-title] The journal of knee surgery
  • [ISO-abbreviation] J Knee Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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41. Jones AC, Prihoda TJ, Kacher JE, Odingo NA, Freedman PD: Osteoblastoma of the maxilla and mandible: a report of 24 cases, review of the literature, and discussion of its relationship to osteoid osteoma of the jaws. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Nov;102(5):639-50
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Osteoblastoma of the maxilla and mandible: a report of 24 cases, review of the literature, and discussion of its relationship to osteoid osteoma of the jaws.
  • Osteoblastoma is a benign neoplasm of bone characterized by a proliferation of osteoblasts forming bone trabeculae set in a vascularized fibrous connective tissue stroma.
  • We report 24 examples of this neoplasm arising in the maxilla and mandible and compare the clinical and radiographic characteristics of this neoplasm to 53 previously reported examples of osteoblastoma and osteoid osteoma in the jaws.
  • Our results reveal more females reported in the new examples of osteoblastoma than in the previously reported examples of osteoblastoma and osteoid osteoma.
  • When all cases are combined, a predominant trend is observed whereby osteoblastoma occurs predominantly on the left side of the posterior mandible and is associated with pain, tenderness, and discomfort.
  • We also provide a rationale for use of the term "osteoblastoma" for any benign osteoblastic neoplasm arising in the jaws.
  • [MeSH-major] Jaw Neoplasms / pathology. Osteoblastoma / pathology. Osteoma, Osteoid / pathology

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  • (PMID = 17052641.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 60
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42. Mirbagheri N, Galloway S, Iseli TA, Lyons BM: Extraosseous osteoblastoma of larynx presenting with acute airway obstruction. J Laryngol Otol; 2008 Nov;122(11):1265-8
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  • [Title] Extraosseous osteoblastoma of larynx presenting with acute airway obstruction.
  • OBJECTIVE: We report the case of an osteoblastoma of the larynx arising from the vocal fold, which presented with acute airway obstruction and cardiopulmonary arrest.
  • METHOD: The histopathological findings, differential diagnoses and a novel method of treating laryngeal osteoblastoma, using transoral laser therapy, are discussed.
  • RESULTS: Benign osteoblastoma is a rare primary bone tumour usually presenting in young patients in the spine and sacrum.
  • Once the diagnosis is confirmed, successful treatment is achieved with surgical excision.
  • CONCLUSION: Osteoblastoma of the larynx is rare, and the clinical features can vary with the anatomical site of the lesion.
  • [MeSH-major] Airway Obstruction / etiology. Laryngeal Neoplasms / complications. Osteoblastoma / complications
  • [MeSH-minor] Aged. Diagnosis, Differential. Humans. Laser Therapy / methods. Male. Treatment Outcome

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  • (PMID = 18289457.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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43. Angiero F, Mellone P, Baldi A, Stefani M: Osteoblastoma of the jaw: report of two cases and review of the literature. In Vivo; 2006 Sep-Oct;20(5):665-70
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  • [Title] Osteoblastoma of the jaw: report of two cases and review of the literature.
  • Osteoblastoma is a benign bone tumor of osteoblastic origin.
  • Differential diagnosis and immunohistochemical features potentially useful for refining diagnosis of osteoblastoma are also discussed.
  • [MeSH-major] Biomarkers, Tumor / analysis. Jaw Neoplasms / pathology. Osteoblastoma / pathology

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  • (PMID = 17091775.001).
  • [ISSN] 0258-851X
  • [Journal-full-title] In vivo (Athens, Greece)
  • [ISO-abbreviation] In Vivo
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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44. Han X, Dong Y, Sun K, Lu Y: A huge occipital osteoblastoma accompanied with aneurysmal bone cyst in the posterior cranial fossa. Clin Neurol Neurosurg; 2008 Mar;110(3):282-5
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  • [Title] A huge occipital osteoblastoma accompanied with aneurysmal bone cyst in the posterior cranial fossa.
  • Osteoblastoma is an infrequent benign tumor and skull involvement is extremely rare.
  • The occipital bone is much less frequently involved.
  • We report an unusual case of a huge occipital osteoblastoma with aneurysmal bone cyst in the posterior cranial fossa of a 20-year-old young man.
  • Pathological examination revealed that the lesion was a benign osteoblastoma with secondary aneurysmal bone cyst (ABC).
  • Despite the benign nature of osteoblastoma, local recurrence after incomplete resection is not rare and malignant transformation during recurrence may occur even after adequate surgery.
  • Our case confirms the findings of previous investigators that if osteoblastoma is removed completely, no recurrence is expected even without adjuvant irradiation and chemotherapy.
  • [MeSH-major] Bone Cysts, Aneurysmal / pathology. Brain Neoplasms / pathology. Occipital Lobe. Osteoblastoma / pathology

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  • (PMID = 18055104.001).
  • [ISSN] 0303-8467
  • [Journal-full-title] Clinical neurology and neurosurgery
  • [ISO-abbreviation] Clin Neurol Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
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45. Papadaki ME, Troulis MJ, Kaban LB: Advances in diagnosis and management of fibro-osseous lesions. Oral Maxillofac Surg Clin North Am; 2005 Nov;17(4):415-34
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Advances in diagnosis and management of fibro-osseous lesions.
  • Fibro-osseous lesions are benign mesenchymal skeletal tumors in which mineralized tissue, blood vessels, and giant cells in varying proportions replace normal bone.
  • Included in this group are fibrous dysplasia, cherubism, ossifying fibromas, and osteoblastoma, with fibrous dysplasia being the most common entity.
  • The purpose of this article is to describe advances in diagnosis and management of fibro-osseous lesions.

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  • (PMID = 18088796.001).
  • [ISSN] 1042-3699
  • [Journal-full-title] Oral and maxillofacial surgery clinics of North America
  • [ISO-abbreviation] Oral Maxillofac Surg Clin North Am
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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46. Herrera Tenorio JG, Núnuez Fernández AI, Mendoza Quiroga JJ, Sesma Villalpando RA: [Benign osteoblastoma in the proximal phalanx. A case report]. Acta Ortop Mex; 2009 Sep-Oct;23(5):298-301
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  • [Title] [Benign osteoblastoma in the proximal phalanx. A case report].
  • [Transliterated title] Osteoblastoma benigno en falange proximal. Reporte de un caso.
  • The purpose of this article is to present a case of phalanx osteoblastoma.
  • We will start by saying that osteoblastoma is rare, it accounts for 1% of primary bone tumors; it is most frequent in the posterior spine, and is very unusual in the phalanges.
  • Early diagnosis is desirable due to its similarity, mainly radiologic, with other entities that result in similar bone lesions.
  • [MeSH-major] Bone Neoplasms. Finger Phalanges. Osteoblastoma

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  • (PMID = 20336881.001).
  • [ISSN] 2306-4102
  • [Journal-full-title] Acta ortopédica mexicana
  • [ISO-abbreviation] Acta Ortop Mex
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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47. Njim L, Dhouibi A, Touil N, Lahmar I, Hadhri R, Moussa A, Zakhama A: Benign osteoblastoma in an unusual mastoid location. Eur Ann Otorhinolaryngol Head Neck Dis; 2010 Nov;127(5):183-5
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  • [Title] Benign osteoblastoma in an unusual mastoid location.
  • INTRODUCTION: Benign osteoblastoma (OB) is an unusual primary bone tumor.
  • We report herein an extremely rare location of an OB in the mastoid process of the temporal bone.
  • The pathologic examination of bone curettage material revealed a benign OB.
  • DISCUSSION/CONCLUSION: To our knowledge, this is the 14th reported case of OB confined to the mastoid process of temporal bone.
  • Its histological diagnosis can be difficult and osteosarcoma is its principal differential diagnosis.
  • Although generally regarded as benign, OB has potential for recurrence and local invasion.
  • [MeSH-major] Bone Neoplasms / diagnosis. Mastoid. Osteoblastoma / diagnosis

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  • [Copyright] Copyright © 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20951662.001).
  • [ISSN] 1879-730X
  • [Journal-full-title] European annals of otorhinolaryngology, head and neck diseases
  • [ISO-abbreviation] Eur Ann Otorhinolaryngol Head Neck Dis
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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48. Pérez-Mora RM, Sanchez-Carrion S, Barea FL, Garcia-Raya P, Lassaletta L: Osteoblastoma of the temporal bone. Skull Base; 2009 Sep;19(5):345-8
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  • [Title] Osteoblastoma of the temporal bone.
  • Benign osteoblastoma is an uncommon primary tumor of the bone.
  • Any area of the skeleton may be affected by this tumor, but its occurrence in the temporal bone and middle ear is extremely rare.
  • Clinical symptoms are nonspecific, even in the middle ear, and the diagnosis is often difficult in spite a complete physical and radiological examination.
  • A biopsy is usually necessary for definitive diagnosis.
  • Because of its potential for recurrence, local invasion, and, rarely, malignant transformation, a complete surgical excision remains the treatment of choice for osteoblastoma.
  • We report a case of benign osteoblastoma involving the temporal bone and the middle ear and a review of the literature.

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  • [Cites] J Pediatr Surg. 2000 Jul;35(7):1127-9 [10917313.001]
  • [Cites] J Laryngol Otol. 1995 Jun;109(6):565-8 [7643005.001]
  • [Cites] AJNR Am J Neuroradiol. 1997 Feb;18(2):324-6 [9111670.001]
  • [Cites] Pathol Res Pract. 1993 Feb;189(1):33-41 [8516215.001]
  • [Cites] Cancer. 1991 Sep 1;68(5):999-1003 [1913494.001]
  • [Cites] J Comput Assist Tomogr. 1985 May-Jun;9(3):577-9 [3989059.001]
  • [Cites] Arch Otolaryngol. 1984 May;110(5):334-6 [6712523.001]
  • [Cites] Am J Otol. 1983 Apr;4(4):318-22 [6859240.001]
  • [Cites] Am J Otolaryngol. 2001 May-Jun;22(3):211-4 [11351292.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • (PMID = 20190944.001).
  • [ISSN] 1532-0065
  • [Journal-full-title] Skull base : official journal of North American Skull Base Society ... [et al.]
  • [ISO-abbreviation] Skull Base
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2765705
  • [Keywords] NOTNLM ; Osteoblastoma / hearing loss / temporal bone / tinnitus
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49. Tugcu B, Gunaldi O, Gunes M, Tanriverdi O, Bilgic B: Osteoblastoma of the temporal bone: a case report. Minim Invasive Neurosurg; 2008 Oct;51(5):310-2
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  • [Title] Osteoblastoma of the temporal bone: a case report.
  • Benign osteoblastoma is an unusual primary bone tumor.
  • Osteoblastoma affecting the calvarium is extremely rare.
  • Computed tomography revealed an expansile, lytic lesion in the left temporal bone.
  • T1- and T2-weighted magnetic resonance (MR) images demonstrated an isointense lesion in the temporal bone.
  • The histopathological findings proved that the lesion was a benign osteoblastoma.
  • To date, very few cases of the benign osteoblastoma arising in the calvarium have been reported in the literature.
  • [MeSH-major] Osteoblastoma / diagnosis. Skull Neoplasms / diagnosis. Temporal Bone
  • [MeSH-minor] Age of Onset. Craniotomy. Diagnosis, Differential. Gadolinium. Humans. Magnetic Resonance Imaging. Male. Neoplasm Invasiveness. Neurosurgical Procedures. Predictive Value of Tests. Preoperative Care. Tomography, X-Ray Computed. Young Adult

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  • (PMID = 18855299.001).
  • [ISSN] 0946-7211
  • [Journal-full-title] Minimally invasive neurosurgery : MIN
  • [ISO-abbreviation] Minim Invasive Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] AU0V1LM3JT / Gadolinium
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50. El-Gammal TA, El-Sayed A, Kotb MM, Saleh WR, Ragheb YF: Knee joint reconstruction after hemiarticular resection using pedicled patella and vascularized fibular graft. Microsurgery; 2010 Nov;30(8):603-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tumor pathology was giant cell tumor in four patients, osteoblastoma in two, and benign fibrous histocytoma in one patient.
  • Average time to bone union was 3.5 months (range, 3-4 months), and average time to full weight-bearing was 5 months (range, 4-6 months).
  • [MeSH-major] Bone Neoplasms / surgery. Giant Cell Tumor of Bone / surgery. Knee Joint / surgery. Surgical Flaps
  • [MeSH-minor] Adolescent. Adult. Female. Histiocytoma, Benign Fibrous / surgery. Humans. Male. Osteoblastoma / surgery. Range of Motion, Articular. Young Adult

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  • [Copyright] Copyright © 2010 Wiley-Liss, Inc.
  • (PMID = 20853338.001).
  • [ISSN] 1098-2752
  • [Journal-full-title] Microsurgery
  • [ISO-abbreviation] Microsurgery
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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51. Chakrapani SD, Grim K, Kaimaktchiev V, Anderson JC: Osteoblastoma of the spine with discordant magnetic resonance imaging and computed tomography imaging features in a child. Spine (Phila Pa 1976); 2008 Dec 1;33(25):E968-70
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  • [Title] Osteoblastoma of the spine with discordant magnetic resonance imaging and computed tomography imaging features in a child.
  • OBJECTIVE: To describe the magnetic resonance imaging (MRI) and computed tomography (CT) findings of spinal osteoblastoma and illustrate how MRI features can be potentially misleading.
  • SUMMARY OF BACKGROUND DATA: Osteoblastoma is a rare benign tumor of bone that is known to incite a localized inflammatory response.
  • These inflammatory features can simulate malignant behavior on MRI and can lead to misdiagnosis and unnecessarily aggressive resection unless one recognizes the classic benign features on CT.
  • We present a case of osteoblastoma in a child to illustrate this concept.
  • A CT demonstrates a well-circumscribed lesion without lytic changes or malignant bone formation.
  • A benign lesion was favored given the CT features and conservative resection was performed.
  • Final pathologic diagnosis was osteoblastoma.
  • CONCLUSION: This case illustrates that the MRI findings for osteoblastoma can be misleading and caution should be used when evaluating benign tumors with known inflammatory responses on MRI.
  • [MeSH-major] Magnetic Resonance Imaging. Osteoblastoma / diagnosis. Spinal Neoplasms / diagnosis. Tomography, X-Ray Computed
  • [MeSH-minor] Child. Diagnosis, Differential. Female. Humans. Inflammation / diagnosis. Inflammation / radiography. Inflammation / surgery. Lumbar Vertebrae / pathology. Lumbar Vertebrae / radiography. Lumbar Vertebrae / surgery

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  • (PMID = 19050575.001).
  • [ISSN] 1528-1159
  • [Journal-full-title] Spine
  • [ISO-abbreviation] Spine
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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52. Folk GS, Williams SB, Foss RB, Fanburg-Smith JC: Oral and maxillofacial sclerosing epithelioid fibrosarcoma: report of five cases. Head Neck Pathol; 2007 Sep;1(1):13-20
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  • Tumor location included the infra-temporal fossa, buccal mucosa (recurrence extending into bone), anterior mandible (intraosseous primary, focally extending into soft tissue), and left parotid and submandibular gland (with metaplastic bone) regions.
  • OMFRSEF occur in adults in various locations, but with a common propensity to involve bone; there is recurrent potential and morbidity with higher grade lesions.
  • The differential diagnosis for these tumors in this site includes sclerosing carcinoma, Ewing/PNET, osteosarcoma, osteoblastoma, and benign and malignant myoepithelial salivary gland tumors.
  • [MeSH-minor] Adult. Apoptosis. Biomarkers, Tumor / metabolism. Diagnosis, Differential. Epithelioid Cells / metabolism. Epithelioid Cells / pathology. Female. Histiocytoma, Benign Fibrous / diagnosis. Humans. Leiomyoma / diagnosis. Male. Middle Aged. Sclerosis. Solitary Fibrous Tumors / diagnosis. Young Adult

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  • [Cites] Cancer Genet Cytogenet. 2000 Jun;119(2):127-31 [10867148.001]
  • [Cites] Cancer. 1989 Aug 15;64(4):925-31 [2545330.001]
  • [Cites] Am J Surg Pathol. 2001 Jun;25(6):699-709 [11395547.001]
  • [Cites] Am J Surg Pathol. 2002 Sep;26(9):1175-83 [12218574.001]
  • [Cites] Int J Surg Pathol. 2002 Jul;10(3):227-30 [12232581.001]
  • [Cites] J Clin Pathol. 2004 Jan;57(1):90-4 [14693846.001]
  • [Cites] Cancer Genet Cytogenet. 2004 Jul 15;152(2):136-40 [15262433.001]
  • [Cites] Virchows Arch. 2004 Oct;445(4):410-3 [15322876.001]
  • [Cites] Neurosurgery. 2000 Oct;47(4):956-9; discussion 959-60 [11014436.001]
  • [Cites] Methods Enzymol. 1990;184:357-63 [1697021.001]
  • [Cites] Am J Surg Pathol. 1995 Sep;19(9):979-93 [7661286.001]
  • [Cites] Histopathology. 1996 May;28(5):451-5 [8735721.001]
  • [Cites] J Clin Oncol. 1997 Jan;15(1):350-62 [8996162.001]
  • [Cites] Histopathology. 1998 Oct;33(4):354-60 [9822926.001]
  • [Cites] Cancer Genet Cytogenet. 1998 Dec;107(2):102-6 [9844602.001]
  • [Cites] Ann Otol Rhinol Laryngol. 2005 Feb;114(2):87-9 [15757185.001]
  • [ErratumIn] Head Neck Pathol. 2013 Mar;7(1):103
  • (PMID = 20614275.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Other-IDs] NLM/ PMC2807507
  • [Keywords] NOTNLM ; Maxillofacial / Oral / Sarcoma / Sclerosing epithelioid fibrosarcoma
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53. Li Y, Liang Q, Wen YQ, Chen LL, Wang LT, Liu YL, Luo CQ, Liang HZ, Li MT, Li Z: Comparative proteomics analysis of human osteosarcomas and benign tumor of bone. Cancer Genet Cytogenet; 2010 Apr 15;198(2):97-106
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  • [Title] Comparative proteomics analysis of human osteosarcomas and benign tumor of bone.
  • Proteins extracted from osteosarcoma tissue and benign bone tumors, including osteoblastoma, chondroblastoma, and giant cell tumor of bone, were examined using two-dimensional gel electrophoresis followed by mass spectrometry analysis and database searches.
  • [MeSH-major] Bone Neoplasms / metabolism. Neoplasm Proteins / analysis. Osteoblastoma / metabolism. Osteosarcoma / metabolism. Proteomics / methods
  • [MeSH-minor] Adolescent. Adult. Aged. Biomarkers, Tumor / analysis. Biomarkers, Tumor / metabolism. Bone and Bones / metabolism. Bone and Bones / pathology. Child. Chondroblastoma / metabolism. Chondroblastoma / pathology. Female. Giant Cell Tumor of Bone / metabolism. Giant Cell Tumor of Bone / pathology. Humans. Male. Middle Aged. Proteome / analysis. Proteome / metabolism. Young Adult


54. Caufourier C, Leprovost N, Guillou-Jamard MR, Compère JF, Bénateau H: [Benign bone forming tumors]. Rev Stomatol Chir Maxillofac; 2009 Sep;110(4):202-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Benign bone forming tumors].
  • Benign bone forming tumors typically produce dense bone (osteoma, enostosis) or osteoid tissue (osteoid osteoma, osteoblastoma).
  • Even though these four lesions have distinct characteristics, it is sometimes difficult to tell them apart and to rule out malignant bone forming lesions such as osteosarcoma.
  • [MeSH-major] Facial Bones / pathology. Skull Neoplasms / diagnosis
  • [MeSH-minor] Adult. Child. Diagnosis, Differential. Exostoses / diagnosis. Fibrous Dysplasia of Bone / diagnosis. Humans. Osteoblastoma / diagnosis. Osteoma / diagnosis. Osteoma, Osteoid / diagnosis. Osteosarcoma / diagnosis

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  • (PMID = 19660772.001).
  • [ISSN] 1776-257X
  • [Journal-full-title] Revue de stomatologie et de chirurgie maxillo-faciale
  • [ISO-abbreviation] Rev Stomatol Chir Maxillofac
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
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55. Samdani A, Torre-Healy A, Chou D, Cahill AM, Storm PB: Treatment of osteoblastoma at C7: a multidisciplinary approach. A case report and review of the literature. Eur Spine J; 2009 Jul;18 Suppl 2:196-200
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  • [Title] Treatment of osteoblastoma at C7: a multidisciplinary approach. A case report and review of the literature.
  • Osteoblastoma is a rare benign bone tumor that presents with back pain and occurs in the spine approximately 40% of the time.
  • The time from onset of symptoms to diagnosis is typically several months because it is a rare entity and radiographic studies are often negative early in the course of the disease.
  • [MeSH-major] Cervical Vertebrae. Embolization, Therapeutic / methods. Osteoblastoma / therapy. Spinal Fusion / methods. Spinal Neoplasms / therapy

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  • [Cites] Neurol India. 1999 Dec;47(4):330-1 [10625912.001]
  • [Cites] Clin Orthop Relat Res. 2007 Feb;455:190-5 [17016229.001]
  • [Cites] Eur J Radiol. 2002 Jul;43(1):79-81 [12065126.001]
  • [Cites] Neoplasma. 2004;51(2):117-26 [15190421.001]
  • [Cites] Neurosurg Focus. 2003 Nov 15;15(5):E5 [15323462.001]
  • [Cites] J Bone Joint Surg Am. 1975 Apr;57(3):424-6 [1123402.001]
  • [Cites] AJR Am J Roentgenol. 1976 Feb;126(2):321-5 [175701.001]
  • [Cites] Clin Orthop Relat Res. 1977 Oct;(128):303-13 [598169.001]
  • [Cites] Clin Orthop Relat Res. 1979 Mar-Apr;(139):133-41 [455830.001]
  • [Cites] J Bone Joint Surg Br. 1984 Jan;66(1):16-20 [6693471.001]
  • [Cites] J Bone Joint Surg Am. 1986 Mar;68(3):354-61 [3949831.001]
  • [Cites] Clin Orthop Relat Res. 1992 May;(278):37-45 [1563167.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Cancer. 1994 May 15;73(10):2653-62 [8174066.001]
  • [Cites] Skeletal Radiol. 1996 Aug;25(6):531-5 [8865486.001]
  • [Cites] Neuroradiology. 1996 Nov;38(8):809-11 [8957812.001]
  • [Cites] Arch Orthop Trauma Surg. 1997;116(5):279-82 [9177804.001]
  • [Cites] J Pediatr Orthop. 1997 Jul-Aug;17(4):440-3 [9364379.001]
  • [Cites] Spine (Phila Pa 1976). 1998 Jan 1;23(1):47-53 [9460152.001]
  • [Cites] Bull Hosp Joint Dis. 1956 Oct;17(2):141-51 [13413389.001]
  • [Cites] Clin Orthop Relat Res. 2005 Apr;(433):171-7 [15805954.001]
  • [Cites] AJNR Am J Neuroradiol. 2006 Oct;27(9):1910-2 [17032864.001]
  • [Cites] Clin Orthop Relat Res. 2002 Apr;(397):394-402 [11953633.001]
  • (PMID = 18839223.001).
  • [ISSN] 1432-0932
  • [Journal-full-title] European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
  • [ISO-abbreviation] Eur Spine J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 25
  • [Other-IDs] NLM/ PMC2899567
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56. Arpino L, Gragnaniello C, Nina P, Franco A: Limited approach to a thoracic spine osteoblastoma. J Neurosurg Sci; 2008 Dec;52(4):123-5; discussion 125
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  • [Title] Limited approach to a thoracic spine osteoblastoma.
  • Osteoblastoma (OB) is a rare primary benign bone tumor.
  • It is important to differentiate OB from osteoid osteoma, a very similar bone tumor.
  • This article describes a 18-year-old female affected from a thoracic osteoblastoma stemming from T9 lamina and extending to T11, with a diameter of about 2.5 cm.
  • OB is rare benign bone neoplasm that generally affect the posterior elements of the spine.
  • [MeSH-major] Neurosurgical Procedures / methods. Osteoblastoma / surgery. Spinal Neoplasms / surgery. Thoracic Vertebrae / surgery

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  • (PMID = 18981987.001).
  • [ISSN] 0390-5616
  • [Journal-full-title] Journal of neurosurgical sciences
  • [ISO-abbreviation] J Neurosurg Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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57. Abolghasemian M, Rezaie M, Behgoo A, Shoushtarizadeh T, Ghazavi MT: Exostosis-like intra-articular periosteal osteoblastoma: a rare case. Am J Orthop (Belle Mead NJ); 2010 Jun;39(6):E50-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Exostosis-like intra-articular periosteal osteoblastoma: a rare case.
  • Osteoblastoma is a relatively rare benign bone tumor, most often located in the vertebral column or metaphysis of the long bones, particularly the femur and the tibia.
  • Periosteal osteoblastoma is the least common type.
  • Exostosis-like appearance is not common even in periosteal osteoblastoma, a very rare type of this tumor.
  • Here we report the case of a 25-year-old man with intra-articular exostosis-like periosteal osteoblastoma of the hip that resulted in impingement and osteoarthritis.
  • [MeSH-major] Bone Neoplasms / pathology. Hip Joint / pathology. Osteoblastoma / pathology. Periosteum / pathology

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  • (PMID = 20631934.001).
  • [ISSN] 1934-3418
  • [Journal-full-title] American journal of orthopedics (Belle Mead, N.J.)
  • [ISO-abbreviation] Am J. Orthop.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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58. Saccomanni B: Osteoid osteoma and osteoblastoma of the spine: a review of the literature. Curr Rev Musculoskelet Med; 2009 Mar;2(1):65-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Osteoid osteoma and osteoblastoma of the spine: a review of the literature.
  • Osteoid osteoma and osteoblastoma are rare primary bone tumors that usually do not arise in the spine.
  • Histologically, osteoid osteoma and osteoblastoma are similar, containing osteoblasts that produce osteoid and woven bone.
  • Osteoblastoma, however, is larger, tends to be more aggressive, and can undergo malignant transformation, whereas osteoid osteoma is small, benign, and self-limited.
  • With the help of modern imaging modalities that aid in diagnosis and surgical planning, a complete removal and cure may be achieved for most of these rare tumors.

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  • [Cites] Spine (Phila Pa 1976). 2003 Nov 15;28(22):E472-7 [14624097.001]
  • [Cites] Clin Orthop Relat Res. 1977 Oct;(128):303-13 [598169.001]
  • [Cites] Radiology. 2002 Jul;224(1):82-6 [12091665.001]
  • [Cites] Spine (Phila Pa 1976). 2000 May 15;25(10):1283-6 [10806507.001]
  • [Cites] Cancer. 1956 Sep-Oct;9(5):1044-52 [13364889.001]
  • [Cites] AJNR Am J Neuroradiol. 1998 Nov-Dec;19(10):1955-8 [9874556.001]
  • [Cites] Eur Spine J. 1998;7(5):422-5 [9840478.001]
  • [Cites] J Med Liban. 1992;40(4):216-8 [1339911.001]
  • [Cites] J Spinal Disord. 1992 Jun;5(2):204-11 [1606380.001]
  • [Cites] Clin Orthop Relat Res. 1992 May;(278):37-45 [1563167.001]
  • [Cites] Spine (Phila Pa 1976). 1990 Dec;15(12):1272-80 [2149206.001]
  • [Cites] Pediatr Radiol. 1986;16(1):25-31 [2935775.001]
  • [Cites] Ital J Orthop Traumatol. 1988 Dec;14(4):527-8 [3267687.001]
  • [Cites] Skeletal Radiol. 1982;9(2):92-7 [7163828.001]
  • [Cites] Neurosurgery. 1981 Jan;8(1):31-8 [7207770.001]
  • [Cites] AJR Am J Roentgenol. 2002 Dec;179(6):1633-42 [12438068.001]
  • (PMID = 19468920.001).
  • [ISSN] 1935-973X
  • [Journal-full-title] Current reviews in musculoskeletal medicine
  • [ISO-abbreviation] Curr Rev Musculoskelet Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2684956
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59. Van Dyck P, Vanhoenacker FM, Vogel J, Venstermans C, Kroon HM, Gielen J, Parizel PM, Bloem JL, De Schepper AM: Prevalence, extension and characteristics of fluid-fluid levels in bone and soft tissue tumors. Eur Radiol; 2006 Dec;16(12):2644-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prevalence, extension and characteristics of fluid-fluid levels in bone and soft tissue tumors.
  • The purpose of this study was to determine the prevalence, extension and signal characteristics of fluid-fluid levels in a large series of 700 bone and 700 soft tissue tumors.
  • Out of a multi-institutional database, MRI of 700 consecutive patients with a bone tumor and MRI of 700 consecutive patients with a soft tissue neoplasm were retrospectively reviewed for the presence of fluid-fluid levels.
  • Of 700 patients with a bone tumor, 19 (10 male and 9 female; mean age, 29 years) presented with a fluid-fluid level (prevalence 2.7%).
  • Diagnoses included aneurysmal bone cyst (ten cases), fibrous dysplasia (two cases), osteoblastoma (one case), simple bone cyst (one case), telangiectatic osteosarcoma (one case), "brown tumor" (one case), chondroblastoma (one case) and giant cell tumor (two cases).
  • Diagnoses included cavernous hemangioma (12 cases), synovial sarcoma (3 cases), angiosarcoma (1 case), aneurysmal bone cyst of soft tissue (1 case), myxofibrosarcoma (1 case) and high-grade sarcoma "not otherwise specified" (2 cases).
  • In our series, the largest reported in the literature to the best of our knowledge, the presence of fluid-fluid levels is a rare finding with a prevalence of 2.7 and 2.9% in bone and soft tissue tumors, respectively.
  • Fluid-fluid levels remain a non-specific finding and can occur in a wide range of bone and soft tissue tumors, both benign and malignant.
  • Therefore, they cannot be considered diagnostic of any particular type of tumor, and the diagnosis should be made on the basis of other radiological and clinical findings.
  • [MeSH-major] Body Fluids / metabolism. Bone Neoplasms / pathology. Magnetic Resonance Imaging / methods. Soft Tissue Neoplasms / pathology

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  • [Cites] Skeletal Radiol. 1994 Feb;23 (2):107-9 [8191292.001]
  • [Cites] AJNR Am J Neuroradiol. 2003 Sep;24(8):1639-41 [13679285.001]
  • [Cites] Eur Radiol. 2004 Oct;14(10):1941-3 [15029449.001]
  • [Cites] Skeletal Radiol. 2003 Dec;32(12 ):701-7 [14564484.001]
  • [Cites] Skeletal Radiol. 2004 Jun;33(6):330-6 [15138727.001]
  • [Cites] AJR Am J Roentgenol. 1993 Oct;161(4):827-30 [8396848.001]
  • [Cites] Eur Radiol. 2004 Mar;14(3):506-13 [14557894.001]
  • [Cites] Skeletal Radiol. 2004 Aug;33(8):477-80 [15150676.001]
  • [Cites] AJR Am J Roentgenol. 1984 May;142(5):1001-4 [6609547.001]
  • [Cites] Skeletal Radiol. 2004 Oct;33(10):582-7 [15316680.001]
  • [Cites] Radiology. 1984 Apr;151(1):51-2 [6701334.001]
  • [Cites] Eur Radiol. 2004 Dec;14(12):2320-30 [15290067.001]
  • [Cites] Eur Radiol. 1998;8(8):1359-62 [9853214.001]
  • [Cites] Skeletal Radiol. 1987;16(3):196-200 [3473690.001]
  • [Cites] Radiology. 1990 Jun;175(3):779-82 [2160676.001]
  • [Cites] Pediatr Radiol. 2000 Aug;30(8):551-7 [10993540.001]
  • [Cites] Br J Radiol. 1992 Mar;65(771):193-8 [1547444.001]
  • [Cites] Br J Radiol. 1971 Jan;44(517):1-13 [5539396.001]
  • [Cites] Eur Radiol. 2001;11(8):1445-9 [11519556.001]
  • (PMID = 16612549.001).
  • [ISSN] 0938-7994
  • [Journal-full-title] European radiology
  • [ISO-abbreviation] Eur Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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60. Ugur HC, Torun F, Kanpolat Y: Petrous bone osteoblastoma invading the cavernous sinus. J Clin Neurosci; 2005 May;12(4):489-92
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  • [Title] Petrous bone osteoblastoma invading the cavernous sinus.
  • A CT scan revealed a mass originating from the petrous part of the temporal bone with infiltration of the cavernous sinus.
  • Pathological examination revealed benign osteoblastoma.
  • [MeSH-major] Bone Neoplasms / pathology. Cavernous Sinus / pathology. Osteoblastoma / pathology. Petrous Bone / pathology

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  • (PMID = 15925793.001).
  • [ISSN] 0967-5868
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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61. Imperiale A, Moser T, Ben-Sellem D, Mertz L, Gangi A, Constantinesco A: Osteoblastoma and osteoid osteoma: morphofunctional characterization by MRI and dynamic F-18 FDG PET/CT before and after radiofrequency ablation. Clin Nucl Med; 2009 Mar;34(3):184-8
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  • [Title] Osteoblastoma and osteoid osteoma: morphofunctional characterization by MRI and dynamic F-18 FDG PET/CT before and after radiofrequency ablation.
  • Osteoblastoma (OB) and osteoid osteoma (OO) are benign bone-forming tumors frequently involving vertebrae and long bones of the extremities.
  • Bone scan is a complementary, highly sensitive functional technique particularly useful for detection of vertebral OO.
  • F-18 FDG PET/CT could have potentiality in diagnosis and post therapeutic evaluation of patients with OB and OO.
  • [MeSH-major] Bone Neoplasms / pathology. Bone Neoplasms / surgery. Fluorodeoxyglucose F18. Osteoblastoma / pathology. Osteoblastoma / surgery. Osteoma, Osteoid / pathology. Osteoma, Osteoid / surgery

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  • (PMID = 19352289.001).
  • [ISSN] 1536-0229
  • [Journal-full-title] Clinical nuclear medicine
  • [ISO-abbreviation] Clin Nucl Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0Z5B2CJX4D / Fluorodeoxyglucose F18
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62. Deyrup AT, Monson DK, Dorfman HD: Aggressive (epithelioid) osteoblastoma arising in soft tissue. Int J Surg Pathol; 2008 Jul;16(3):308-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Aggressive (epithelioid) osteoblastoma arising in soft tissue.
  • Aggressive (epithelioid) osteoblastoma arising in soft tissue has never been described.
  • It is important to differentiate this benign osteoblastoma, a potentially locally aggressive tumor, from extraskeletal osteosarcoma.
  • This report describes an aggressive (epithelioid) osteoblastoma arising in a focus of heterotopic ossification in the axilla of a 21-year-old man.
  • [MeSH-major] Bone Neoplasms / diagnosis. Epithelioid Cells / pathology. Ossification, Heterotopic / pathology. Osteoblastoma / diagnosis. Soft Tissue Neoplasms / diagnosis

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  • (PMID = 18573786.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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63. Combalia Aleu A, Popescu D, Pomes J, Palacin A: Long-standing pain in a 25-year-old patient with a non-diagnosed cervical osteoblastoma: a case report. Arch Orthop Trauma Surg; 2008 Jun;128(6):567-71
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Long-standing pain in a 25-year-old patient with a non-diagnosed cervical osteoblastoma: a case report.
  • Benign osteoblastomas are infrequent tumors, representing less than 1% of all bone tumors.
  • We present a case report of a young male that due to the lack of specific symptoms was diagnosed of a cervical osteoblastoma 14 months after the first symptoms.
  • Nowadays, this delay in diagnosis may be avoided by the routine use of MRI or CT for unspecific cervical symptoms.
  • [MeSH-major] Cervical Vertebrae. Osteoblastoma / diagnosis. Spinal Neoplasms / diagnosis

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  • (PMID = 17641905.001).
  • [ISSN] 0936-8051
  • [Journal-full-title] Archives of orthopaedic and trauma surgery
  • [ISO-abbreviation] Arch Orthop Trauma Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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64. O'Dwyer HM, Keogh CF, O'Connell JX, Munk PL: A case report of synchronous osteoblastoma and fibromatosis. Br J Radiol; 2008 Mar;81(963):e68-71
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  • [Title] A case report of synchronous osteoblastoma and fibromatosis.
  • Osteoblastoma is a rare bone tumour that accounts for 1% of all primary bone tumours and 3% of all benign bone tumours.
  • Osteoblastoma occurring in long bones has a predilection for the meta-diaphysis.
  • It bears a close histological resemblance to osteoid osteoma, but it is not growth limited - usually 2 cm or greater at diagnosis.
  • The term "fibromatosis" covers a broad spectrum of benign fibrous tissue proliferations.
  • To our knowledge, this is the first case report in the English literature of a patient with synchronous presentation of an osteoblastoma and fibromatosis.
  • [MeSH-major] Femoral Neoplasms / pathology. Fibroma / pathology. Neoplasms, Multiple Primary / pathology. Osteoblastoma / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Thigh. Tomography, X-Ray Computed

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  • (PMID = 18270286.001).
  • [ISSN] 1748-880X
  • [Journal-full-title] The British journal of radiology
  • [ISO-abbreviation] Br J Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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65. Dancer JY, Henry SP, Bondaruk J, Lee S, Ayala AG, de Crombrugghe B, Czerniak B: Expression of master regulatory genes controlling skeletal development in benign cartilage and bone forming tumors. Hum Pathol; 2010 Dec;41(12):1788-93
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  • [Title] Expression of master regulatory genes controlling skeletal development in benign cartilage and bone forming tumors.
  • The present study evaluates the expression of these factors in 4 types of benign bone tumors-chondromyxoid fibroma, chondroblastoma, osteoid osteoma, and osteoblastoma-using immunohistochemistry and tissue microarrays.
  • Osteoid osteoma and osteoblastoma showed strong nuclear expression of Osterix and Runx2.
  • [MeSH-major] Bone Neoplasms / genetics. Cartilage / growth & development. Gene Regulatory Networks. Neoplasms, Connective Tissue / genetics. Osteogenesis / genetics. Transcription Factors / genetics
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Chondroblastoma / genetics. Chondroblastoma / metabolism. Chondroblastoma / pathology. Chondroma / genetics. Chondroma / metabolism. Chondroma / pathology. Core Binding Factor Alpha 1 Subunit / genetics. Core Binding Factor Alpha 1 Subunit / metabolism. Female. Fibroma / genetics. Fibroma / metabolism. Fibroma / pathology. Gene Expression Regulation. Humans. Male. Middle Aged. Osteoblastoma / genetics. Osteoblastoma / metabolism. Osteoblastoma / pathology. Osteoma, Osteoid / genetics. Osteoma, Osteoid / metabolism. Osteoma, Osteoid / pathology. SOX9 Transcription Factor / genetics. SOX9 Transcription Factor / metabolism. Stem Cells / metabolism. Stem Cells / pathology. Tissue Array Analysis. Young Adult

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  • [Copyright] Copyright © 2010 Elsevier Inc. All rights reserved.
  • [Cites] Genes Dev. 2001 Feb 15;15(4):467-81 [11230154.001]
  • [Cites] Hum Pathol. 2010 Feb;41(2):208-13 [19801163.001]
  • [Cites] Hum Pathol. 2003 Mar;34(3):263-9 [12673561.001]
  • [Cites] J Bone Miner Metab. 2003;21(4):193-7 [12811622.001]
  • [Cites] J Biol Chem. 2003 Jun 27;278(26):23971-7 [12697767.001]
  • [Cites] Trends Genet. 2003 Aug;19(8):458-66 [12902164.001]
  • [Cites] Gene. 2004 Jul 7;336(1):115-25 [15225881.001]
  • [Cites] Mol Cell Biol. 1997 Apr;17(4):2336-46 [9121483.001]
  • [Cites] EMBO J. 1998 Oct 1;17(19):5718-33 [9755172.001]
  • [Cites] Nat Genet. 1999 May;22(1):85-9 [10319868.001]
  • [Cites] J Biol Chem. 1999 Aug 20;274(34):24023-30 [10446171.001]
  • [Cites] J Cell Biol. 2004 Dec 6;167(5):925-34 [15583032.001]
  • [Cites] Cancer Res. 2005 Feb 15;65(4):1124-8 [15734992.001]
  • [Cites] Lab Invest. 2005 Apr;85(4):532-49 [15778693.001]
  • [Cites] Nat Med. 2005 Aug;11(8):880-5 [16041384.001]
  • [Cites] Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14665-70 [16203988.001]
  • [Cites] Eur J Med Res. 2005 Nov 16;10(11):475-9 [16354601.001]
  • [Cites] Gene. 2006 May 10;372:62-70 [16574347.001]
  • [Cites] Genes Dev. 2006 Nov 1;20(21):2937-42 [17050674.001]
  • [Cites] Adv Exp Med Biol. 2006;585:431-41 [17120800.001]
  • [Cites] Rev Endocr Metab Disord. 2006 Jun;7(1-2):1-16 [17051438.001]
  • [Cites] Pathol Oncol Res. 2007;13(1):32-7 [17387386.001]
  • [Cites] Mol Cancer Res. 2008 Jan;6(1):119-26 [18234967.001]
  • [Cites] Oncogene. 2008 Jun 5;27(25):3605-14 [18223689.001]
  • [Cites] Annu Rev Genomics Hum Genet. 2008;9:183-96 [18767962.001]
  • [Cites] J Bone Miner Res. 2009 Jun;24(6):1055-65 [19113927.001]
  • [Cites] Tumori. 2009 May-Jun;95(3):311-6 [19688969.001]
  • [Cites] Am J Med Genet A. 2009 Dec;149A(12):2882-5 [19921652.001]
  • [Cites] Cell. 2002 Jan 11;108(1):17-29 [11792318.001]
  • (PMID = 21078438.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Grant] United States / NIAMS NIH HHS / AR / R01 AR049072
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Core Binding Factor Alpha 1 Subunit; 0 / RUNX2 protein, human; 0 / SOX9 Transcription Factor; 0 / SOX9 protein, human; 0 / Sp7 protein, human; 0 / Transcription Factors
  • [Other-IDs] NLM/ NIHMS574893; NLM/ PMC4012830
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66. Narita T, Ishii N, Mayuzumi H, Kobayashi H, Ikeda J, Iwasaki Y: Occipitoparietal benign osteoblastoma: should entire lesion be resected when magnetic resonance images reveal wide abnormal signal intensity in surrounding bone marrow? Surg Neurol; 2005 Aug;64(2):180-3; discussion 184
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Occipitoparietal benign osteoblastoma: should entire lesion be resected when magnetic resonance images reveal wide abnormal signal intensity in surrounding bone marrow?
  • BACKGROUND: Benign osteoblastoma is an uncommon primary bone tumor that usually affects long bones and the vertebral column.
  • Despite the characteristically benign nomenclature of osteoblastoma, it sometimes recurs with the possibility of transforming into a malignant form after an incomplete resection.
  • However, it has not been clarified whether the adjacent bones should also be completely resected when magnetic resonance (MR) images reveal abnormal signal intensity in the bone marrow.
  • CASE DESCRIPTION: Presented in this case report is a 12-year-old boy with occipital tenderness associated with occipitoparietal bone tumor.
  • Neuroradiological studies demonstrated a solid tumor located in the occipital bone extending over the right parietal bone.
  • Magnetic resonance images further revealed abnormal signal intensity in the bone marrow of the entire occipital and bilateral parietal bones.
  • Macroscopically, the calvarial bone adjacent to the solid tumor appeared to be reddish, but it was not covering the entire area, contradicting the abnormal intensity found on the preoperative MR images.
  • Although MR images revealed abnormal intensity in the bone marrow of the surgical margin immediately after the operation, the intensity had been normalized by degrees and there was no evidence of recurrence during a follow-up period of 34 months.
  • This may suggest that bone marrow lesion showing abnormal intensity was edema rather than tumor invasion.
  • CONCLUSIONS: The authors conclude that total resection, including a bone marrow lesion, is not always necessary for benign osteoblastoma.
  • Macroscopic findings that show an abnormal color tone of the cortex could be a good indicator in revealing tumor activity invading bone marrow.
  • [MeSH-major] Magnetic Resonance Imaging. Occipital Bone / pathology. Osteoblastoma / pathology. Osteoblastoma / surgery. Skull Neoplasms / pathology. Skull Neoplasms / surgery
  • [MeSH-minor] Bone Marrow Neoplasms / pathology. Child. Humans. Male. Neoplasm Invasiveness. Neoplasm Staging

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  • (PMID = 16051019.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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67. Nishida K, Doita M, Kawahara N, Tomita K, Kurosaka M: Total en bloc spondylectomy in the treatment of aggressive osteoblastoma of the thoracic spine. Orthopedics; 2008 Apr;31(4):403
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  • [Title] Total en bloc spondylectomy in the treatment of aggressive osteoblastoma of the thoracic spine.
  • Osteoblastoma is an uncommon, benign osteoblastic tumor accounting for <1% of all primary bone tumors.
  • Aggressive osteoblastoma is a variant of osteoblastoma and is considered to be a borderline or intermediate osteoblastic tumor, first defined by Dorfman and Weiss in 1984.
  • Treatment of osteoblastoma is complete surgical excision by either curettage or en bloc technique.
  • Recurrence is seen in 10% to 15% of cases, and aggressive osteoblastoma are more likely to recur (<or=50%).
  • Therefore, total en bloc spondylectomy constitutes the treatment of choice for recurrent aggressive osteoblastoma.
  • This article reports a rare case of recurrent aggressive osteoblastoma of the thoracic spine, successfully treated by total en bloc spondylectomy.
  • Treatment options for such a highly recurrent benign tumor are discussed.
  • [MeSH-major] Laminectomy / methods. Neoplasm Recurrence, Local / prevention & control. Osteoblastoma / surgery. Spinal Neoplasms / surgery. Thoracic Vertebrae / surgery

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  • (PMID = 19292265.001).
  • [ISSN] 0147-7447
  • [Journal-full-title] Orthopedics
  • [ISO-abbreviation] Orthopedics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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68. Gomez-Brouchet A, Mourcin F, Gourraud PA, Bouvier C, De Pinieux G, Le Guelec S, Brousset P, Delisle MB, Schiff C: Galectin-1 is a powerful marker to distinguish chondroblastic osteosarcoma and conventional chondrosarcoma. Hum Pathol; 2010 Sep;41(9):1220-30
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  • The clinical management of osteosarcoma differs significantly from that of chondrosarcoma; therefore, it is extremely important to diagnose these 2 types of bone tumor accurately.
  • In the absence of a specific marker, differential diagnosis by histochemistry is sometimes impossible, especially between chondroblastic osteosarcoma and conventional chondrosarcoma.
  • We analyzed 165 bone sarcomas by immunohistochemical staining of tissue microarrays for expression of the galectin-1 (GAL1) lectin and by Western blot experiments.
  • We found that GAL1 was abundant in normal human osteoblasts from benign proliferations and in osteosarcomas, including chondroblastic osteosarcomas, but not in chondrosarcomas.
  • We propose a diagnostic test for bone tumors that takes into account the optimal discriminative values for the percentage of cells stained and the intensity of staining.
  • [MeSH-major] Biomarkers, Tumor / metabolism. Bone Neoplasms / diagnosis. Chondrosarcoma / diagnosis. Galectin 1 / metabolism. Osteosarcoma / diagnosis
  • [MeSH-minor] Adolescent. Blotting, Western. Cell Count. Chondrocytes / metabolism. Chondrocytes / pathology. Diagnosis, Differential. Female. Humans. Immunoenzyme Techniques. Male. Middle Aged. Osteoblastoma / metabolism. Osteoblastoma / pathology. Periostitis / metabolism. Periostitis / pathology. Tissue Array Analysis


69. Guo Z, Wang Z, Li J, Li XD: [Reconstruction with a new type of combined reconstruction following excision of periacetabular tumors]. Zhonghua Wai Ke Za Zhi; 2008 Jun 15;46(12):895-9
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  • Other primary tumors were 2 giant cell tumors and 1 aggressive osteoblastoma.
  • Three metastatic bone tumors were also included in this study, and the original sites were thyroid, breast, and ovary.
  • Three primary benign bone tumors belonged to stage III.
  • [MeSH-major] Acetabulum. Bone Neoplasms / surgery. Reconstructive Surgical Procedures / methods
  • [MeSH-minor] Adolescent. Adult. Aged. Arthroplasty, Replacement, Hip. Bone Screws. Female. Follow-Up Studies. Humans. Male. Middle Aged. Treatment Outcome

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  • (PMID = 19035146.001).
  • [ISSN] 0529-5815
  • [Journal-full-title] Zhonghua wai ke za zhi [Chinese journal of surgery]
  • [ISO-abbreviation] Zhonghua Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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70. Moon KS, Jung S, Lee JH, Jung TY, Kim IY, Kim SH, Kang SS: Benign osteoblastoma of the occipital bone: case report and literature review. Neuropathology; 2006 Apr;26(2):141-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign osteoblastoma of the occipital bone: case report and literature review.
  • We present a case of benign osteoblastoma of the occipital bone.
  • Benign osteoblastoma is an uncommon primary bone tumor, which usually involves the vertebrae and the long bones.
  • To the best of our knowledge, this case is only the eighth reported case of benign osteoblastoma confined to the occipital bone.
  • However, it was very difficult to formulate a differential diagnosis against other osteoblastic tumors, or osteoid osteoma, in view of its radiological appearance.
  • The final diagnosis was obtained by careful consideration of the histopathological characteristics of the tumor combined with its clinical and radiological features.
  • Although generally regarded as benign, a complete resection is preferred over conventional curettage as this can guard against possible recurrence and malignant transformation.
  • [MeSH-major] Occipital Bone / pathology. Osteoblastoma / pathology. Skull Neoplasms / pathology

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  • (PMID = 16708546.001).
  • [ISSN] 0919-6544
  • [Journal-full-title] Neuropathology : official journal of the Japanese Society of Neuropathology
  • [ISO-abbreviation] Neuropathology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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71. Gibson SE, Prayson RA: Primary skull lesions in the pediatric population: a 25-year experience. Arch Pathol Lab Med; 2007 May;131(5):761-6
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  • The differential diagnosis of these lesions is broad and includes both congenital and acquired lesions.
  • RESULTS: Nineteen primary skull lesions were identified in 11 male (58%) and 8 female (42%) patients, with a median age at diagnosis of 9.5 years.
  • These lesions were usually benign and most commonly presented as a painless mass (n = 8).
  • The lesions were located in the occipital bone (n = 7), frontal bone (n = 5), parietal bone (n = 2), and temporal bone (n = 1).
  • Diagnoses included epidermoid/dermoid cyst (n = 8), Langerhans cell histiocytosis (n = 6), intraosseous hemangioma (n = 2), osteoblastoma (n = 1), infantile myofibroma (n = 1), and fibroma (n = 1).
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Diagnosis, Differential. Female. Humans. Infant. Infant, Newborn. Male. Retrospective Studies

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  • (PMID = 17488162.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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72. Aydeniz A, Erkutlu I, Altindağ O, Küçükoğlu B, Gürsoy S: Severe neck and back pain in adolescence: remember osteoblastoma. Rheumatol Int; 2010 Jul;30(9):1243-4
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  • [Title] Severe neck and back pain in adolescence: remember osteoblastoma.
  • Osteoblastoma is a rare benign tumor of the bone.
  • The tumor was resected by a spinal surgeon and histologic examination revealed osteoblastoma.
  • [MeSH-major] Osteoblastoma / pathology. Osteoblastoma / surgery. Spinal Neoplasms / pathology. Spinal Neoplasms / surgery

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  • [Cites] Am J Phys Med Rehabil. 2003 Oct;82(10):820-3 [14508414.001]
  • [Cites] Spine (Phila Pa 1976). 2006 Nov 1;31(23 ):E895-9 [17077728.001]
  • [Cites] Radiology. 1990 Jun;175(3):783-90 [2343130.001]
  • [Cites] Clin Orthop Relat Res. 2002 Apr;(397):394-402 [11953633.001]
  • [Cites] Yale J Biol Med. 2001 Jan-Feb;74(1):1-8 [11249234.001]
  • [Cites] J Pediatr Orthop. 2008 Jul-Aug;28(5):555-60 [18580372.001]
  • [Cites] Clin Orthop Relat Res. 1977 Oct;(128):303-13 [598169.001]
  • [Cites] Radiographics. 1996 Sep;16(5):1131-58 [8888395.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Neurosurg Focus. 2003 Nov 15;15(5):E5 [15323462.001]
  • (PMID = 19582457.001).
  • [ISSN] 1437-160X
  • [Journal-full-title] Rheumatology international
  • [ISO-abbreviation] Rheumatol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


73. Emmez H, Kaymaz M, Tokgöz N, Yilmaz G, Kurt G: Progression of a lumbar spinal osteoblastoma. Neurol Med Chir (Tokyo); 2005 Jul;45(7):379-83
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  • [Title] Progression of a lumbar spinal osteoblastoma.
  • A 24-year-old woman presented with a lumbar spinal osteoblastoma manifesting as a 5-year history of low back pain radiating to the left foot.
  • Primary benign bone tumors such as osteoblastoma and osteoid osteoma should be considered in the differential diagnosis of back pain and the patients should be followed up carefully.
  • [MeSH-major] Lumbar Vertebrae. Magnetic Resonance Imaging. Osteoblastoma / diagnosis. Radionuclide Imaging. Spinal Neoplasms / diagnosis. Tomography, X-Ray Computed

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  • (PMID = 16041187.001).
  • [ISSN] 0470-8105
  • [Journal-full-title] Neurologia medico-chirurgica
  • [ISO-abbreviation] Neurol. Med. Chir. (Tokyo)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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74. Gdoura F, Trigui M, Ellouze Z, Hamed YB, Ayadi K, Keskes H: Hamatum osteoblastoma. Orthop Traumatol Surg Res; 2010 Oct;96(6):712-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Hamatum osteoblastoma.
  • We report the case of an osteoblastoma of the hamate bone that was successfully treated by curettage.
  • This tumor is very rare in a carpal bone and only nine cases have been reported in the literature.
  • Osteoblastomas are benign, but potentially aggressive bone tumors.
  • [MeSH-major] Bone Neoplasms / surgery. Hamate Bone / surgery. Osteoblastoma / surgery
  • [MeSH-minor] Adult. Biopsy. Bone Cysts / diagnosis. Bone Cysts / pathology. Bone Cysts / surgery. Curettage. Delayed Diagnosis. Humans. Magnetic Resonance Imaging. Male. Osteolysis / diagnosis. Osteolysis / pathology. Osteolysis / surgery

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  • [Copyright] Copyright © 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20692218.001).
  • [ISSN] 1877-0568
  • [Journal-full-title] Orthopaedics & traumatology, surgery & research : OTSR
  • [ISO-abbreviation] Orthop Traumatol Surg Res
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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75. Shimizu N, Sakata K, Yamamoto I: Benign osteoblastoma of the temporal bone: Case report and review of the literature. Surg Neurol; 2006 Nov;66(5):534-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign osteoblastoma of the temporal bone: Case report and review of the literature.
  • BACKGROUND: Benign osteoblastoma arising from the temporal bone is extremely rare in elderly patients.
  • We reviewed the literature on benign osteoblastoma of the temporal bone and now propose a new classification of this pathologic entity based on its anatomical location in the temporal bone.
  • Preoperative computed tomography showed a bony destructive isodensity mass with calcified component involving the temporal bone.
  • The pathologic examination revealed a benign osteoblastoma.
  • [MeSH-major] Bone Neoplasms / diagnosis. Osteoblastoma / diagnosis. Temporal Bone / pathology. Temporal Bone / radiography

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  • (PMID = 17084206.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0Z5B2CJX4D / Fluorodeoxyglucose F18
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76. Puri A, Agarwal MG, Shah M, Srinivas CH, Shukla PJ, Shrikhande SV, Jambhekar NA: Decision making in primary sacral tumors. Spine J; 2009 May;9(5):396-403
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The diagnosis included chordoma in six patients, giant cell tumor in seven patients, aneurysmal bone cyst in two patients, and a chondrosarcoma and an osteoblastoma in one patient each.
  • Six benign lesions were treated with curettage.
  • CONCLUSION: Wide resection with adequate margins gives the best chance of local control and should be the surgery of choice for all malignant primary sacral tumors and in benign lesions involving lower segments when preservation of both S3 roots is possible.
  • To retain bladder and bowel control and minimize neurological dysfunction, it may be worthwhile managing benign sacral tumors that extend above S3 with serial embolization.

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  • (PMID = 19059810.001).
  • [ISSN] 1878-1632
  • [Journal-full-title] The spine journal : official journal of the North American Spine Society
  • [ISO-abbreviation] Spine J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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77. Dellmann A, Schroeder HG, Donhuijsen K: Destructive tumours of the larynx mimicking osteosarcoma: two cases of osteoblastoma with organ-saving resection and follow-up. Eur Arch Otorhinolaryngol; 2010 Jan;267(1):151-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Destructive tumours of the larynx mimicking osteosarcoma: two cases of osteoblastoma with organ-saving resection and follow-up.
  • Osteoblastoma of the larynx is an extremely rare type of locally progressive and destructive tumour which is mimicking osteosarcoma radiologically and histologically.
  • Since prognostic and therapeutic strategies for benign osteoblastoma differ from the more common osteosarcoma of the larynx, a meticulous pre-operative histological diagnosis is required to avoid over-therapy.
  • We report about two patients with osteoblastoma of the larynx with organ-saving resection and long-period follow-up without tumour recurrence.
  • This situation is quite different from the usual osteoblastomas of bone, which occur in young adults of both sexes equally.
  • [MeSH-major] Laryngeal Neoplasms / surgery. Laryngectomy / methods. Osteoblastoma / surgery. Osteosarcoma / diagnosis
  • [MeSH-minor] Aged. Biopsy. Diagnosis, Differential. Follow-Up Studies. Humans. Laryngoscopy. Male. Tomography, X-Ray Computed

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  • [Cites] Laryngoscope. 2005 Jan;115(1):74-7 [15630370.001]
  • [Cites] Pathol Res Pract. 1993 Feb;189(1):33-41 [8516215.001]
  • [Cites] Head Neck. 1997 Mar;19(2):153-7 [9059875.001]
  • [Cites] Int J Surg Pathol. 2005 Oct;13(4):365-7 [16273197.001]
  • [Cites] Hum Pathol. 2006 Jul;37(7):890-8 [16784990.001]
  • [Cites] J Laryngol Otol. 2008 Nov;122(11):1265-8 [18289457.001]
  • [Cites] Vestn Otorinolaringol. 1966 Nov-Dec;28(6):69-71 [5252225.001]
  • [Cites] Otolaryngol Pol. 2006;60(2):227-8 [16903343.001]
  • [Cites] Hum Pathol. 1999 Oct;30(10 ):1254-9 [10534176.001]
  • [Cites] J Comput Assist Tomogr. 1996 Jan-Feb;20(1):116-8 [8576460.001]
  • [Cites] Semin Diagn Pathol. 1984 Aug;1(3):215-34 [6600112.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • (PMID = 19760213.001).
  • [ISSN] 1434-4726
  • [Journal-full-title] European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
  • [ISO-abbreviation] Eur Arch Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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78. Kaya A, Altay T, Sezak M, Ozturk H: Periosteal osteoblastoma of the distal femur. Acta Orthop Belg; 2009 Apr;75(2):280-5
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  • [Title] Periosteal osteoblastoma of the distal femur.
  • Periosteal osteoblastoma is a rare benign osteoblastic bone tumour located on the cortical bone.
  • We report a case of periosteal osteoblastoma located at the distal femur in a 31-year-old man.
  • Clinical, radiological and histopathologic findings are described and differential diagnosis is discussed.
  • Despite its rarity, periosteal osteoblastoma should be considered as a possible diagnosis together with periostitis ossificans, periosteal chondroma, periosteal osteosarcoma and parosteal osteosarcoma when confronted with a superficial bone lesion.
  • [MeSH-major] Femoral Neoplasms / diagnosis. Osteoblastoma / diagnosis. Periosteum
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. Tomography, X-Ray Computed

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  • (PMID = 19492573.001).
  • [ISSN] 0001-6462
  • [Journal-full-title] Acta orthopaedica Belgica
  • [ISO-abbreviation] Acta Orthop Belg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
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79. Tarantino R, Piccirilli M, Anichini G, Delfini R: Benign osteoblastoma of the odontoid process of the axis with secondary aneurysmal bone cyst component: a case report. Neurosurg Rev; 2008 Jan;31(1):111-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign osteoblastoma of the odontoid process of the axis with secondary aneurysmal bone cyst component: a case report.
  • The authors report their experience on one patient with osteoblatoma of the odontoid process of the axis with secondary aneurysmal bone cyst.
  • Because of the rarity of this lesion, it was difficult to have a certain preoperative diagnosis.
  • The intraoperative histological examination showed the benign nature of the lesion.
  • The histological examination revealed an osteoblastoma of the odontoid process of the axis with a secondary aneurysmal bone cyst.
  • [MeSH-major] Bone Cysts, Aneurysmal / complications. Odontoid Process. Osteoblastoma / complications. Spinal Neoplasms / complications

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  • [Cites] J Neurosurg. 1988 Dec;69(6):895-903 [3193195.001]
  • [Cites] Am J Surg Pathol. 1996 Jul;20(7):841-50 [8669532.001]
  • [Cites] AJR Am J Roentgenol. 1998 Nov;171(5):1244 [9798854.001]
  • [Cites] J Comput Tomogr. 1985 Oct;9(4):347-50 [4053663.001]
  • [Cites] Neurosurgery. 1989 Jan;24(1):37-42 [2927597.001]
  • [Cites] Clin Radiol. 1996 Sep;51(9):644-8 [8810695.001]
  • [Cites] J Bone Joint Surg Br. 1986 May;68(3):350-6 [3733795.001]
  • [Cites] Neurosurgery. 1991 Apr;28(4):592-4 [2034356.001]
  • [Cites] J Bone Joint Surg Am. 1975 Jan;57(1):1-9 [1123354.001]
  • [Cites] Clin Orthop Relat Res. 1992 May;(278):37-45 [1563167.001]
  • [Cites] Acta Neurochir (Wien). 1992;118(3-4):112-6 [1456094.001]
  • [Cites] Clin Imaging. 2001 Jul-Aug;25(4):247-50 [11566084.001]
  • [Cites] Skeletal Radiol. 1989;18(6):475-80 [2814559.001]
  • [Cites] J Bone Joint Surg Am. 1964 Jun;46:755-65 [14161088.001]
  • [Cites] AJR Am J Roentgenol. 1995 Mar;164(3):573-80 [7863874.001]
  • [Cites] Neurosurgery. 1978 Sep-Oct;3(2):201-7 [703938.001]
  • [Cites] Bull Hosp Joint Dis. 1956 Oct;17(2):141-51 [13413389.001]
  • [Cites] Ann R Coll Surg Engl. 1985 Sep;67(5):321-5 [3901865.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Cancer. 1956 Sep-Oct;9(5):1044-52 [13364889.001]
  • [Cites] J Bone Joint Surg Br. 1978 Aug;60-B(3):406-11 [681419.001]
  • [Cites] Ann Surg. 1893 Jul;18(1):8-17 [17859952.001]
  • [Cites] Oral Surg Oral Med Oral Pathol. 1993 Oct;76(4):433-6 [8233421.001]
  • [Cites] Neuroradiology. 1999 Apr;41(4):279-82 [10344515.001]
  • [Cites] Neurosurgery. 1987 Jan;20(1):52-5 [3808275.001]
  • [Cites] Spine (Phila Pa 1976). 1979 Nov-Dec;4(6):506-10 [515842.001]
  • [Cites] Surg Neurol. 1998 Mar;49(3):274-7 [9508114.001]
  • [Cites] Neurosurgery. 2003 Jan;52(1):247-50; discussion 251 [12493127.001]
  • (PMID = 17960438.001).
  • [ISSN] 0344-5607
  • [Journal-full-title] Neurosurgical review
  • [ISO-abbreviation] Neurosurg Rev
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


80. Kyriakos M, El-Khoury GY, McDonald DJ, Buckwalter JA, Sundaram M, DeYoung B, O'Brien MP: Osteoblastomatosis of bone. A benign, multifocal osteoblastic lesion, distinct from osteoid osteoma and osteoblastoma, radiologically simulating a vascular tumor. Skeletal Radiol; 2007 Mar;36(3):237-47
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Osteoblastomatosis of bone. A benign, multifocal osteoblastic lesion, distinct from osteoid osteoma and osteoblastoma, radiologically simulating a vascular tumor.
  • Histologically, the individual lesions had the features of the nidus of osteoid osteoma/osteoblastoma.
  • The process is designated as osteoblastomatosis to indicate its bone-forming character, prominent osteoblast proliferation, and multiplicity.
  • The cases are distinguished from multifocal/multicentric osteoid osteoma and osteoblastoma, and from benign and malignant vascular tumors.
  • [MeSH-major] Bone Neoplasms / diagnosis. Leg Bones / pathology. Osteoblastoma / diagnosis
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Female. Humans. Magnetic Resonance Imaging. Male. Osteoma, Osteoid / diagnosis. Vascular Neoplasms / diagnosis

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  • [Cites] J Bone Joint Surg Am. 1954 Jun;36-A(3):559-72 [13163088.001]
  • [Cites] Arch Surg. 1949 Mar;58(3):318-27 [18124832.001]
  • [Cites] Clin Orthop Relat Res. 1989 Nov;(248):163-8 [2805475.001]
  • [Cites] Skeletal Radiol. 2003 Jul;32(7):412-5 [12851789.001]
  • [Cites] Am J Roentgenol Radium Ther Nucl Med. 1974 May;121(1):103-6 [4833895.001]
  • [Cites] Skeletal Radiol. 1994 Oct;23 (7):565-8 [7824988.001]
  • [Cites] Ital J Orthop Traumatol. 1984 Jun;10 (2):257-60 [6469612.001]
  • [Cites] Int Orthop. 1996;20(1):61-3 [8881894.001]
  • [Cites] Am J Surg Pathol. 1986 Nov;10 (11):754-64 [2430475.001]
  • [Cites] AJR Am J Roentgenol. 1976 Feb;126(2):321-5 [175701.001]
  • [Cites] J Bone Joint Surg Am. 1982 Jun;64(5):779-80 [7085705.001]
  • [Cites] J Bone Joint Surg Am. 1993 Apr;75(4):597-602 [8478388.001]
  • [Cites] Skeletal Radiol. 2000 Feb;29(2):63-74 [10741493.001]
  • [Cites] Acta Orthop Scand. 1970;41(3):272-91 [5486182.001]
  • [Cites] Skeletal Radiol. 1994 Aug;23 (6):465-7 [7992115.001]
  • [Cites] Skeletal Radiol. 1994 May;23 (4):247-52 [8059248.001]
  • [Cites] Pediatr Radiol. 2004 Mar;34(3):280 [14513298.001]
  • [Cites] J Craniomaxillofac Surg. 1991 May;19(4):166-71 [1880210.001]
  • [Cites] J Bone Joint Surg Am. 1964 Jun;46:755-65 [14161088.001]
  • [Cites] J Hand Surg Am. 1978 May;3(3):280-3 [350949.001]
  • [Cites] J Can Assoc Radiol. 1976 Dec;27(4):298-300 [993245.001]
  • [Cites] Skeletal Radiol. 1996 Oct;25(7):667-70 [8915053.001]
  • [Cites] Bull Hosp Joint Dis. 1956 Oct;17(2):141-51 [13413389.001]
  • [Cites] J Bone Joint Surg Am. 1991 Apr;73(4):612-4 [2013603.001]
  • [Cites] Acta Radiol. 1991 Jan;32(1):62-6 [2012734.001]
  • [Cites] J Hand Surg Am. 1989 May;14 (3):538-41 [2738342.001]
  • [Cites] Skeletal Radiol. 2000 Oct;29(10 ):601-4 [11127685.001]
  • [Cites] Am J Surg Pathol. 1993 Jun;17 (6):610-7 [8333560.001]
  • [Cites] Clin Orthop Relat Res. 1972;85:82-97 [5036935.001]
  • [Cites] J Bone Joint Surg Am. 1973 Jun;55(4):855-8 [4283763.001]
  • [Cites] Skeletal Radiol. 1993 Oct;22(7):485-500 [8272884.001]
  • [Cites] Semin Diagn Pathol. 1984 Aug;1(3):215-34 [6600112.001]
  • [Cites] Hum Pathol. 1994 Feb;25(2):117-34 [8119712.001]
  • [Cites] Cancer. 1956 Sep-Oct;9(5):1044-52 [13364889.001]
  • [Cites] J Bone Joint Surg Am. 1982 Oct;64(8):1243 [7130236.001]
  • [Cites] J Bone Joint Surg Br. 1978 Feb;60(1):100-6 [627569.001]
  • [Cites] Orthopedics. 2004 Dec;27(12 ):1294-6 [15633962.001]
  • [Cites] Skeletal Radiol. 1996 Apr;25(3):287-93 [8741070.001]
  • [Cites] Cancer. 1982 Sep 1;50(5):970-81 [7093931.001]
  • [Cites] Am J Surg Pathol. 1996 Nov;20(11):1301-11 [8898834.001]
  • [Cites] J Bone Joint Surg Am. 1947 Oct;29(4):918-30 [20270357.001]
  • [Cites] J Bone Joint Surg Am. 1975 Mar;57(2):159-63 [1112842.001]
  • (PMID = 16639626.001).
  • [ISSN] 0364-2348
  • [Journal-full-title] Skeletal radiology
  • [ISO-abbreviation] Skeletal Radiol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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81. Khin YT, Peh WC, Lee VK, Teo HE, Ng SB, Nathan SS: Aggressive osteoblastoma of the proximal humerus. Singapore Med J; 2009 Jan;50(1):e1-4
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  • [Title] Aggressive osteoblastoma of the proximal humerus.
  • Bone scintiscan showed solitary marked uptake.
  • The final diagnosis was osteoblastoma with aggressive features.
  • Osteoblastoma is a relatively rare benign tumour that typically occurs in the posterior elements of the vertebral column.
  • [MeSH-major] Bone Neoplasms / diagnosis. Humerus. Osteoblastoma / diagnosis
  • [MeSH-minor] Child. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. Tomography, Emission-Computed

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  • (PMID = 19224061.001).
  • [ISSN] 0037-5675
  • [Journal-full-title] Singapore medical journal
  • [ISO-abbreviation] Singapore Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Singapore
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82. Louaste J, Amhajji L, Chkoura M, Rachid K: [Osteoblastoma in the proximal radio ulnar joint]. Chir Main; 2007 Apr;26(2):117-9
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  • [Title] [Osteoblastoma in the proximal radio ulnar joint].
  • Osteoblastoma is a benign but painful bone tumour, which can only be treated surgically.
  • A delay in diagnosis can, despite successful treatment of the tumour, cause loss of the full range of movements of the elbow.
  • [MeSH-major] Elbow Joint. Osteoblastoma

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  • (PMID = 17470420.001).
  • [ISSN] 1297-3203
  • [Journal-full-title] Chirurgie de la main
  • [ISO-abbreviation] Chir Main
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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83. Zon Filippi R, Swee RG, Krishnan Unni K: Epithelioid multinodular osteoblastoma: a clinicopathologic analysis of 26 cases. Am J Surg Pathol; 2007 Aug;31(8):1265-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Epithelioid multinodular osteoblastoma: a clinicopathologic analysis of 26 cases.
  • Of the 23 patients with osteoblastoma whose sex had been recorded, 18 were male and 5 were female (median age, 17.8 y).
  • Radiologic studies suggested a benign lesion in 5 patients, a malignant lesion in 2, and indeterminate features in 2.
  • Histologically, the tumors appeared to be multiple nodules of epithelioid cells, most with a lacy, blue-bone matrix.
  • Although follow-up is limited, we are cautiously optimistic that these are benign lesions.
  • [MeSH-major] Bone Neoplasms / pathology. Epithelioid Cells / pathology. Osteoblastoma / pathology. Osteoblasts / pathology

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  • (PMID = 17667552.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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84. Alvares Capelozza AL, Gião Dezotti MS, Casati Alvares L, Negrão Fleury R, Sant'Ana E: Osteoblastoma of the mandible: systematic review of the literature and report of a case. Dentomaxillofac Radiol; 2005 Jan;34(1):1-8
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  • [Title] Osteoblastoma of the mandible: systematic review of the literature and report of a case.
  • Benign osteoblastoma is a bone tumour that seldom occurs in the facial bones.
  • A new case of benign osteoblastoma is presented and clinical, radiographic and microscopic aspects, as well as differential diagnosis, treatment and follow-up are discussed.
  • The importance of the correct diagnosis of this type of lesion is stressed, since it presents a clinical, radiographic and microscopic similarity to other bone lesions, including malignant tumours, which may lead the professional into conducting the case in an improper manner.
  • [MeSH-major] Mandibular Neoplasms / radiography. Osteoblastoma / radiography
  • [MeSH-minor] Child. Diagnosis, Differential. Humans. Male

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  • (PMID = 15709098.001).
  • [ISSN] 0250-832X
  • [Journal-full-title] Dento maxillo facial radiology
  • [ISO-abbreviation] Dentomaxillofac Radiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 69
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