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Items 1 to 38 of about 38
1. Sepah YJ, Umer M, Minhas K, Hafeez K: Chondroblastoma of the cuboid with an associated aneurysmal bone cyst: a case report. J Med Case Rep; 2007;1:135
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We report the case of a young adult who presented with a painful foot due to chondroblastoma associated with an aneurismal bone cyst.Chondroblastoma is a rare benign cartilaginous neoplasm that accounts for approximately 1% of all bone tumors and characteristically arises in the epiphysis of a long bone, particularly the humerus, tibia, and femur.

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  • (PMID = 17999776.001).
  • [ISSN] 1752-1947
  • [Journal-full-title] Journal of medical case reports
  • [ISO-abbreviation] J Med Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2194702
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2. Sohn SH, Koh SA, Kim DG, Park SW, Lee KH, Kim MK, Choi JH, Hyun MS: A case of spine origin chondroblastoma metastasis to lung. Cancer Res Treat; 2009 Dec;41(4):241-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondroblastoma is a rare benign cartilaginous neoplasm that accounts for approximately 1% of all bone tumors and characteristically arises in the epiphysis of a long bone, particularly the humerus, tibia, and femur.
  • Unlike previously published examples of metastatic chondroblastoma, these metastasis developed before any operative manipulation of the primary tumor.
  • And primary tumor site was also unusual.

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  • (PMID = 20057972.001).
  • [ISSN] 2005-9256
  • [Journal-full-title] Cancer research and treatment : official journal of Korean Cancer Association
  • [ISO-abbreviation] Cancer Res Treat
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2802843
  • [Keywords] NOTNLM ; Chondroblastoma / Lung metastasis / Spine origin
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3. Bullock RW, Soares DP, Shah S: Subpubic cartilaginous cyst: an unusual cause of a vulval mass. BMJ Case Rep; 2009;2009

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  • [Title] Subpubic cartilaginous cyst: an unusual cause of a vulval mass.
  • The mass did not show typical clinical features of a vulval neoplasm.
  • A literature review revealed characteristics of this lesion compatible with a subpubic cartilaginous cyst-a rare benign degenerative condition of the symphysis pubis.

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  • (PMID = 21686400.001).
  • [ISSN] 1757-790X
  • [Journal-full-title] BMJ case reports
  • [ISO-abbreviation] BMJ Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC3027660
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4. Thompson LD, Karamurzin Y, Wu ML, Kim JH: Solitary fibrous tumor of the larynx. Head Neck Pathol; 2008 Jun;2(2):67-74
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  • [Title] Solitary fibrous tumor of the larynx.
  • BACKGROUND: True mesenchymal, non-cartilaginous neoplasms of the larynx are rare.
  • Extrapleural solitary fibrous tumor (SFT) is a localized neoplasm characterized by proliferation of thin-walled vessels and collagen-producing cells and is considered within the "hemangiopericytoma-solitary fibrous tumor" spectrum.
  • A cellular, spindle cell neoplasm was arranged in loose fascicles, associated with heavy collagen fiber deposition.
  • These findings confirmed a diagnosis of extraplural solitary fibrous tumor.
  • CONCLUSIONS: The characteristic histologic pattern of solitary fibrous tumor can be noted in extrapulmonary locations.
  • Development in the larynx is uncommon, but the tumor presents as a polypoid mass with characteristic histologic and immunophenotypic features.
  • [MeSH-major] Laryngeal Neoplasms / pathology. Solitary Fibrous Tumors / pathology
  • [MeSH-minor] Biomarkers, Tumor / metabolism. Disease-Free Survival. Humans. Male. Middle Aged. Treatment Outcome

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  • (PMID = 20614325.001).
  • [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/ PMC2807554
  • [Keywords] NOTNLM ; Benign neoplasm / CD34 / Fibroma / Hemangiopericytoma / Immunohistochemistry / Larynx / Mesenchymal tumor / Prognosis / Solitary fibrous tumor / Spindle cell squamous cell carcinoma / Surgery / True vocal cord / bcl-2
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5. Gelderblom H, Hogendoorn PC, Dijkstra SD, van Rijswijk CS, Krol AD, Taminiau AH, Bovée JV: The clinical approach towards chondrosarcoma. Oncologist; 2008 Mar;13(3):320-9
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  • Chondrosarcomas that arise de novo are primary chondrosarcomas, whereas chondrosarcomas developing superimposed on pre-existing benign cartilage neoplasms such as enchondromas or osteochondromas are referred to as secondary chondrosarcomas.
  • [MeSH-major] Bone Neoplasms / therapy. Chondrosarcoma, Mesenchymal / therapy

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  • [ErratumIn] Oncologist. 2008 May;13(5):618
  • (PMID = 18378543.001).
  • [ISSN] 1083-7159
  • [Journal-full-title] The oncologist
  • [ISO-abbreviation] Oncologist
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 91
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6. Zustin J, Akpalo H, Gambarotti M, Priemel M, Rueger JM, Luebke AM, Reske D, Lange C, Pueschel K, Lohmann C, Rüther W, Amling M, Alberghini M: Phenotypic diversity in chondromyxoid fibroma reveals differentiation pattern of tumor mimicking fetal cartilage canals development: an immunohistochemical study. Am J Pathol; 2010 Sep;177(3):1072-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Phenotypic diversity in chondromyxoid fibroma reveals differentiation pattern of tumor mimicking fetal cartilage canals development: an immunohistochemical study.
  • Chondromyxoid fibroma represents a rare benign cartilaginous tumor of young patients occurring in a subcortical metaphyseal location.
  • The histogenesis of chondromyxoid fibroma has not yet been postulated, even though the conventional histology and recent immunohistochemical studies on phenotype of the mesenchymal cells and extracellular matrix components suggested its origin in immature cartilage.
  • Therefore, we wished to compare the morphological pattern of immature cartilage tissue with chondromyxoid fibroma to investigate a possible developmental counterpart of chondromyxoid fibroma.
  • Vascularized cartilage canals growing into the fetal cartilage from the perichondrium displayed characteristic glomeruloid structures with central arterioles within the immature mesenchymal stroma and numerous superficial sinusoidal blood vessels accompanied by macrophage infiltration.
  • Based on the observed substantial morphological similarity between the cartilage canals and chondromyxoid fibroma, we suggest that the chondromyxoid fibroma represents a neoplasm originating from or mimicking the fetal cartilage canals within the immature cartilage.
  • [MeSH-major] Cartilage / pathology. Chondroma / pathology. Femoral Neoplasms / pathology. Fibroma / pathology

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  • (PMID = 20671262.001).
  • [ISSN] 1525-2191
  • [Journal-full-title] The American journal of pathology
  • [ISO-abbreviation] Am. J. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2928941
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7. Chamberlain AM, Anderson KL, Hoch B, Trumble TE, Weisstein JS: Benign parosteal osteochondromatous proliferation of the hand originally diagnosed as osteochondroma: a report of two cases and review. Hand (N Y); 2010 Mar;5(1):106-10

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign parosteal osteochondromatous proliferation of the hand originally diagnosed as osteochondroma: a report of two cases and review.
  • Bizarre parosteal osteochondromatous proliferation (BPOP) is a rare cartilaginous neoplasm that often presents in the long bones of the hands and feet.
  • BPOP is a benign but locally aggressive fibro-osseous mass that has striking clinical, radiographic, and histologic similarities with osteochondroma.

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  • (PMID = 19669236.001).
  • [ISSN] 1558-9455
  • [Journal-full-title] Hand (New York, N.Y.)
  • [ISO-abbreviation] Hand (N Y)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2820629
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8. Yalniz E, Alicioglu B, Yalcin O, Yilmaz B: Non specific magnetic resonance features of chondromyxoid fibroma of the iliac bone. J BUON; 2007 Jul-Sep;12(3):407-9
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  • Chondromyxoid fibroma is a benign cartilaginous neoplasm.
  • The tumor is rare, perhaps the rarest of all bone tumors.
  • [MeSH-major] Bone Neoplasms / diagnosis. Chondroma / diagnosis. Fibroma / diagnosis. Ilium. Magnetic Resonance Imaging

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  • (PMID = 17918298.001).
  • [ISSN] 1107-0625
  • [Journal-full-title] Journal of B.U.ON. : official journal of the Balkan Union of Oncology
  • [ISO-abbreviation] J BUON
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
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9. Karkuzhali P, Chithralekha S, Muthuvel E, Daniel RB: Chondromyxoid fibroma of the parietal bone. Neuropathology; 2005 Mar;25(1):84-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma is a benign cartilaginous neoplasm, which can be easily mistaken for chondrosarcoma, especially in small biopsies.
  • [MeSH-major] Chondroblastoma / pathology. Parietal Bone / pathology. Skull Neoplasms / pathology

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  • (PMID = 15822822.001).
  • [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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10. Yang SW, Lin CY: A peculiar site of chondroma: the epiglottis. Acta Otolaryngol; 2005 Aug;125(8):906-9
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  • Chondroma of the laryngeal cartilage is an uncommon benign cartilaginous neoplasm.
  • The commonest location is the posterior lamina of the cricoid cartilage, followed by the thyroid cartilage.
  • We present this case to highlight the occurrence of this rare benign lesion in the epiglottis, and stress that it should not be neglected in the differential diagnosis of an epiglottic mass.
  • [MeSH-major] Chondroma / diagnosis. Epiglottis / surgery. Laryngeal Neoplasms / diagnosis

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  • (PMID = 16158541.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Norway
  • [Number-of-references] 11
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11. Vialle R, Feydy A, Rillardon L, Tohme-Noun C, Anract P, Colombat M, De Pinieux G, Drapé JL, Guigui P: Chondroblastoma of the lumbar spine. Report of two cases and review of the literature. J Neurosurg Spine; 2005 May;2(5):596-600
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  • Chondroblastoma is a benign cartilaginous neoplasm that generally affects the appendicular skeleton.
  • Magnetic resonance imaging allowed the authors to study the tumor's local extension.
  • [MeSH-major] Chondroblastoma / pathology. Chondroblastoma / surgery. Spinal Fusion. Spinal Neoplasms / pathology. Spinal Neoplasms / surgery
  • [MeSH-minor] Adult. Female. Humans. Low Back Pain / etiology. Lumbar Vertebrae / pathology. Lumbar Vertebrae / surgery. Magnetic Resonance Imaging. Middle Aged. Neoplasm Recurrence, Local

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  • (PMID = 15945435.001).
  • [ISSN] 1547-5654
  • [Journal-full-title] Journal of neurosurgery. Spine
  • [ISO-abbreviation] J Neurosurg Spine
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 21
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12. Stanić V, Vulović T, Stamenović D, Dordević G: Use of Marlex mesh with methylmethacrylate to repair large full-thickness defects after subtotal sternectomy caused by chondroma. Vojnosanit Pregl; 2008 Feb;65(2):175-7
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  • BACKGROUND: Sternal benign neoplasms are extremely rare.
  • Chondroma is a benign tumor of cartilage and can be single or multple.
  • CASE REPORT: We presented a case of 28-year-old woman with chondroma of the sternum treated by "en bloc" resection of the tumor (subtotal sternectomy).
  • [MeSH-major] Bone Neoplasms / surgery. Chondroma / surgery. Methylmethacrylate. Polypropylenes. Sternum. Surgical Mesh. Thoracic Wall / surgery

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  • (PMID = 18365678.001).
  • [ISSN] 0042-8450
  • [Journal-full-title] Vojnosanitetski pregled
  • [ISO-abbreviation] Vojnosanit Pregl
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Serbia
  • [Chemical-registry-number] 0 / Polypropylenes; 196OC77688 / Methylmethacrylate
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13. Alman BA, Wunder JS: Parathyroid hormone-related protein regulates glioma-associated oncogene transcriptional activation: lessons learned from bone development and cartilage neoplasia. Ann N Y Acad Sci; 2008 Nov;1144:36-41
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  • [Title] Parathyroid hormone-related protein regulates glioma-associated oncogene transcriptional activation: lessons learned from bone development and cartilage neoplasia.
  • By studying the interaction of the pathways in normal and neoplastic growth-plate chondrocytes (from enchondromas, a benign cartilage tumor), an unexpected direct regulation of hedgehog-mediated transcriptional activation by parathyroid hormone-related protein was uncovered.
  • [MeSH-major] Bone Development / genetics. Bone Neoplasms / metabolism. Cartilage / metabolism. Chondroma / metabolism. Chondrosarcoma / metabolism. Parathyroid Hormone-Related Protein / metabolism. Transcription Factors / metabolism. Transcriptional Activation

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  • (PMID = 19076361.001).
  • [ISSN] 1749-6632
  • [Journal-full-title] Annals of the New York Academy of Sciences
  • [ISO-abbreviation] Ann. N. Y. Acad. Sci.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Hedgehog Proteins; 0 / Parathyroid Hormone-Related Protein; 0 / Transcription Factors
  • [Number-of-references] 32
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14. Falcone G, Rossi ED, Maccauro G, de Santis V, Rosa MA, Capelli A, Fadda G: Diagnostic relevance of the immunohistochemical detection of growth factors in benign and malignant cartilaginous tumors. Appl Immunohistochem Mol Morphol; 2006 Sep;14(3):334-40
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  • [Title] Diagnostic relevance of the immunohistochemical detection of growth factors in benign and malignant cartilaginous tumors.
  • The goal of this study was to evaluate the diagnostic relevance of the expression of growth factors in cartilaginous tumors and to investigate on the possible correlation with grade, local recurrence, metastatic potential, and survival.
  • Expression of VEGF, PDGF, FGF1, TFGbeta2, TNFalpha, Ki-67, and p53 was analyzed in 21 cases of benign and malignant cartilaginous tumors using immunohistochemistry.
  • These data suggest a progressive modification in the biologic behavior of malignant cartilaginous tumors.

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  • (PMID = 16932026.001).
  • [ISSN] 1541-2016
  • [Journal-full-title] Applied immunohistochemistry & molecular morphology : AIMM
  • [ISO-abbreviation] Appl. Immunohistochem. Mol. Morphol.
  • [Language] ENG
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Growth Substances
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15. Rau T, Soeder S, Olk A, Aigner T: Parosteal lipoma of the thigh with cartilaginous and osseous differentiation: an osteochondrolipoma. Ann Diagn Pathol; 2006 Oct;10(5):279-82

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Parosteal lipoma of the thigh with cartilaginous and osseous differentiation: an osteochondrolipoma.
  • Lipomas are very common benign soft tissue neoplasms.
  • Mature cartilage and bone arising in a lipoma is a rare event and is mostly associated with a parosteal localization of the neoplasm.
  • We describe a new case of osteochondrolipoma showing not only major adipocytic differentiation but also areas of fibrocytic and cartilaginous cell differentiation and bone formation (both endochondral and membranous).
  • The occurrence of at least 4 distinct directions of mesenchymal cell differentiation within a benign neoplasia underlines the concept of multilineage differentiation of pluripotent mesenchymal stem cells.
  • [MeSH-major] Bone and Bones / pathology. Cartilage / pathology. Lipoma / pathology. Periosteum / pathology. Soft Tissue Neoplasms / pathology

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  • (PMID = 16979520.001).
  • [ISSN] 1092-9134
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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16. 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.
  • [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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17. Röpke M, Boltze C, Meyer B, Neumann HW, Roessner A, Schneider-Stock R: Rb-loss is associated with high malignancy in chondrosarcoma. Oncol Rep; 2006 Jan;15(1):89-95
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  • We studied the loss of heterozygosity (LOH) of the Rb gene in 31 formalin-fixed, paraffin-embedded cartilaginous tumors using polymerase chain reaction.
  • The only case of DD chondrosarcoma negative for Rb-LOH in both components of the tumor also showed weak expression of the Rb protein in the anaplastic component.
  • All benign cartilaginous tumors, low-grade chondrosarcomas and low-grade tumor components of DD chondrosarcomas were negative regarding Rb-LOH but positive in Rb immunohistostaining.
  • [MeSH-major] Bone Neoplasms / diagnosis. Chondrosarcoma / diagnosis. Genes, Retinoblastoma / genetics. Loss of Heterozygosity / genetics
  • [MeSH-minor] Adolescent. Adult. Aged. Child. DNA, Neoplasm / analysis. Female. Humans. Immunohistochemistry. Male. Middle Aged. Polymerase Chain Reaction. Prognosis. Retinoblastoma Protein / analysis. Retinoblastoma Protein / genetics

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  • (PMID = 16328039.001).
  • [ISSN] 1021-335X
  • [Journal-full-title] Oncology reports
  • [ISO-abbreviation] Oncol. Rep.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / DNA, Neoplasm; 0 / Retinoblastoma Protein
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18. Kim CW, Oh SJ, Rho YS, Cho SJ, Koh ES: A case of dysplastic nevus of the external auditory canal presenting with conductive hearing loss. Yonsei Med J; 2009 Dec 31;50(6):845-7
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  • A nevus which is a benign melanocytic neoplasm rarely occurs within the external auditory canal (EAC).
  • Physical examination revealed a protruding mass arising from the posterior wall of the left cartilaginous EAC.

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  • [Cites] Arch Dermatol. 2001 Jul;137(7):917-20 [11453811.001]
  • [Cites] Ear Nose Throat J. 2003 Jan;82(1):38-41 [12610902.001]
  • [Cites] Arch Dermatol. 2003 Mar;139(3):282-8 [12622618.001]
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  • [Cites] Mod Pathol. 2006 Feb;19 Suppl 2:S4-20 [16446715.001]
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  • [Cites] J Otolaryngol. 1988 Aug;17(5):241-3 [3216448.001]
  • (PMID = 20046428.001).
  • [ISSN] 1976-2437
  • [Journal-full-title] Yonsei medical journal
  • [ISO-abbreviation] Yonsei Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2796414
  • [Keywords] NOTNLM ; External auditory canal / conductive hearing loss / dysplastic nevus / intradermal nevus
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19. Smith CA, Magenis RE, Himoe E, Smith C, Mansoor A: Chondromyxoid fibroma of the nasal cavity with an interstitial insertion between chromosomes 6 and 19. Cancer Genet Cytogenet; 2006 Dec;171(2):97-100
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma is an uncommon benign cartilaginous tumor that rarely presents in the sino-nasal region as a locally destructive, erosive lesion.
  • Histology of the tumor, especially with a small sample, can be challenging because of its heterogeneous nature showing an admixture of fibrous, myxoid, and chondroid areas.
  • These results illustrate the distinctive nature of this tumor and may help identify genes involved in the pathogenesis of this tumor.
  • [MeSH-major] Chromosomes, Human, Pair 19. Chromosomes, Human, Pair 6. DNA Transposable Elements. Fibroma / genetics. Nasal Cavity. Nose Neoplasms / genetics. Translocation, Genetic

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  • (PMID = 17116486.001).
  • [ISSN] 0165-4608
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA Transposable Elements
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20. Fulciniti F, Mansueto G, Vetrani A, Accurso A, Fortunato A, Palombini L: Metaplastic breast carcinoma on fine-needle cytology samples: a report of three cases. Diagn Cytopathol; 2005 Sep;33(3):205-9
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  • Because of the various presentation of MBC on fine-needle cytology samples and the possible influence of needle "sampling" on the cytological specimen, the spectrum of differential diagnoses to be considered may encompass a number of benign and malignant entities, like keratinous subareolar cysts, malignant fibroepithelial lesions with myxo-chondroid stroma, and true sarcomas of the breast, with cartilaginous metaplasia.
  • [MeSH-major] Breast Neoplasms / pathology. Neoplasm Metastasis / pathology

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  • [Copyright] Copyright (c) 2005 Wiley-Liss, Inc.
  • (PMID = 16078244.001).
  • [ISSN] 8755-1039
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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21. Ayers LS, Depasquale K, Marlowe FI, Ghaderi M: Pleomorphic adenoma of the external auditory canal: a case report and review of the literature. Ear Nose Throat J; 2010 Mar;89(3):E1-3
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  • Pleomorphic adenomas of the external auditory canal (EAC) are benign tumors of the ceruminal glands; they are a rare entity.
  • Arising from the lateral cartilaginous portion of the EAC, these lesions can be challenging to diagnose in view of their rare clinical presentation, indolent symptoms, and a lack of familiarity on the part of histopathologists.
  • We report the case of a pleomorphic adenoma in a 32-year-old woman, and we review the literature on glandular neoplasms of the EAC, with particular emphasis on terminology and factors that can hinder the diagnosis.
  • [MeSH-major] Adenoma, Pleomorphic / pathology. Ear, External / pathology. Salivary Gland Neoplasms / pathology
  • [MeSH-minor] Adult. Female. Humans. Neoplasm Invasiveness

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  • (PMID = 20229463.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 10
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22. Rodriguez FJ, Aubry MC, Tazelaar HD, Slezak J, Carney JA: Pulmonary chondroma: a tumor associated with Carney triad and different from pulmonary hamartoma. Am J Surg Pathol; 2007 Dec;31(12):1844-53
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  • [Title] Pulmonary chondroma: a tumor associated with Carney triad and different from pulmonary hamartoma.
  • The Carney triad is the clinical association of gastric stromal sarcomas, pulmonary cartilaginous tumors, and extra-adrenal paragangliomas.
  • The pulmonary tumors are its second commonest component and have been misinterpreted clinically and pathologically as metastases from the gastric tumors and pulmonary cartilaginous hamartomas, respectively.
  • They have not been previously described in detail in the pathology literature or compared with pulmonary cartilaginous hamartomas.
  • Forty-two patients with pulmonary cartilaginous tumors as a component of Carney triad were identified.
  • Hematoxylin and eosin-stained sections of the neoplasms were evaluated for a series of histologic features.
  • A subgroup of 41 tumors from the latter was compared with those in a group of pulmonary cartilaginous hamartomas.
  • Their pulmonary neoplasm(s) were usually asymptomatic, often multiple, well circumscribed, medium-sized (mean diameter=2.8 cm), and composed almost exclusively of cartilage and bone surrounded by a fibrous pseudocapsule.
  • The cartilage was usually myxoid, less frequently hyaline, and commonly calcified, ossified, or both.
  • The pulmonary neoplasms in the Carney triad are well-differentiated benign cartilaginous tumors that are best designated as chondromas.
  • They differ pathologically from pulmonary cartilaginous hamartomas on the basis of the presence of a thin fibrous pseudocapsule, frequent bone metaplasia, and calcification, and also the absence of entrapped epithelium and fat.
  • [MeSH-major] Chondroma / pathology. Hamartoma / pathology. Lung Neoplasms / pathology. Neoplasms, Multiple Primary / pathology

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  • (PMID = 18043038.001).
  • [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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23. Veras EF, Santamaria IB, Luna MA: Sinonasal chondromyxoid fibroma. Ann Diagn Pathol; 2009 Feb;13(1):41-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma (CMF) is a rare benign cartilaginous tumor that usually arises from the metaphysis of long bones.
  • The initial radiographic findings were suggestive of a vascular tumor or a malignancy, but microscopic examination revealed the typical pathologic features of CMF, and SOX9 immunostaining confirmed its cartilaginous origin.
  • The tumor was successfully excised, and the patient was free of disease at 12-month follow-up.
  • [MeSH-major] Chondroma / pathology. Fibroma / pathology. Nasal Septum / pathology. Paranasal Sinus Neoplasms / pathology

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  • (PMID = 19118781.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / SOX9 Transcription Factor; 0 / SOX9 protein, human
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24. Saini R, Abd Razak NH, Ab Rahman S, Samsudin AR: Chondrosarcoma of the mandible: a case report. J Can Dent Assoc; 2007 Mar;73(2):175-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondrosarcomas are malignant tumours of cartilaginous origin.
  • They range from a well-differentiated growth resembling a benign cartilage tumour to a high-grade malignancy with aggressive local behaviour and the potential to metastasize.
  • [MeSH-major] Chondrosarcoma / pathology. Mandibular Neoplasms / pathology
  • [MeSH-minor] Adult. Female. Humans. Neoplasm, Residual / radiotherapy

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  • (PMID = 17355810.001).
  • [ISSN] 1488-2159
  • [Journal-full-title] Journal (Canadian Dental Association)
  • [ISO-abbreviation] J Can Dent Assoc
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Canada
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25. Oliveira RC, Marques KD, Mendonça AR, Mendonça EF, Silva MR, Batista AC, Ribeiro-Rotta RF: Chondrosarcoma of the temporomandibular joint: a case report in a child. J Orofac Pain; 2009;23(3):275-81
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  • Chondrosarcoma is a malignant cartilaginous neoplasm that resembles synovial chondromatosis.
  • Microscopic findings showed a tumor exhibiting cartilaginous tissue proliferation with cellular pleomorphism, nuclear hyperchromasia, and mixoid changes in the matrix.
  • It is concluded that cartilaginous lesions in the jaws must be regarded with suspicion, since benign and malignant lesions may show similar clinical features.

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  • (PMID = 19639107.001).
  • [ISSN] 1064-6655
  • [Journal-full-title] Journal of orofacial pain
  • [ISO-abbreviation] J Orofac Pain
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CCNB1 protein, human; 0 / Cyclin B; 0 / Cyclin B1; 0 / Ki-67 Antigen
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26. Hakan T, Vardar Aker F: Chondromyxoid fibroma of frontal bone: a case report and review of the literature. Turk Neurosurg; 2008 Jul;18(3):249-53

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma is an unusual benign tumor of cartilaginous tissues that may be confused with other some malign tumors.
  • The patient underwent tumor excision with craniectomy, then acrylic cranioplasty.
  • In conclusion, chondromyxoid fibroma is a benign primary bone tumor that is located extremely rarely in the frontal bone.
  • En block surgical resection of the tumor is the cornerstone of treatment.
  • [MeSH-major] Chondroma / pathology. Fibroma / pathology. Frontal Bone / pathology. Skull Neoplasms / pathology

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  • (PMID = 18814113.001).
  • [ISSN] 1019-5149
  • [Journal-full-title] Turkish neurosurgery
  • [ISO-abbreviation] Turk Neurosurg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Turkey
  • [Number-of-references] 22
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27. Romeo S, Bovée JV, Grogan SP, Taminiau AH, Eilers PH, Cleton-Jansen AM, Mainil-Varlet P, Hogendoorn PC: Chondromyxoid fibroma resembles in vitro chondrogenesis, but differs in expression of signalling molecules. J Pathol; 2005 Jun;206(2):135-42
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  • Chondromyxoid fibroma is a rare benign cartilaginous bone tumour characterized by morphological features that resemble different steps of chondrogenesis in terms of both cellular morphology, ranging from spindled to rounded cells, and the extracellular matrix formed, which ranges from fibrous to cartilaginous.
  • The presence in chondromyxoid fibroma of signalling molecules that regulate the spatial expression of proteins involved in normal cartilage proliferation and differentiation was investigated in samples from 20 patients and compared with articular chondrocytes from 11 normal donors cultivated in 3D pellet culture.
  • Morphological similarities reflect common steps in cartilage differentiation, albeit driven by different molecular mechanisms.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology. Chondrogenesis
  • [MeSH-minor] Cartilage, Articular / cytology. Cell Cycle Proteins / metabolism. Cells, Cultured. Chondrocytes / cytology. Female. Humans. Immunoenzyme Techniques. Male. Neoplasm Proteins / metabolism. Signal Transduction

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  • [Copyright] Copyright 2005 Pathological Society of Great Britain and Ireland
  • (PMID = 15880456.001).
  • [ISSN] 0022-3417
  • [Journal-full-title] The Journal of pathology
  • [ISO-abbreviation] J. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Cell Cycle Proteins; 0 / Neoplasm Proteins
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28. Ozbudak IH, Dertsiz L, Bassorgun CI, Ozbilim G: Giant cystic chondroid hamartoma of the lung. J Pediatr Surg; 2008 Oct;43(10):1909-11
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  • Pulmonary hamartoma composed of an abnormal mixture of mesenchymal elements is the most common benign neoplasm in the lung.
  • Multilocular cystic spaces with intervening lobulated fragments of cartilaginous tissue and adipose tissue were seen.
  • Microscopically, the solid component was composed of cartilage and adipose tissue.
  • [MeSH-minor] Adipose Tissue / pathology. Calcinosis / pathology. Calcinosis / radiography. Calcinosis / surgery. Cartilage / pathology. Child. Diagnosis, Differential. Epithelium / pathology. Humans. Incidental Findings. Lung Neoplasms / diagnosis. Male. Thoracotomy. Tomography, X-Ray Computed

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  • (PMID = 18926231.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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29. Luevitoonvechkij S, Arphornchayanon O, Leerapun T, Khunsree S: Periosteal chondroma of the proximal humerus: a case report and review of the literature. J Med Assoc Thai; 2006 Nov;89(11):1970-5
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  • Periosteal chondroma is a slow growing benign cartilaginous tumor of bone.
  • [MeSH-major] Bone Neoplasms / surgery. Chondroma / surgery. Humerus

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  • (PMID = 17205883.001).
  • [ISSN] 0125-2208
  • [Journal-full-title] Journal of the Medical Association of Thailand = Chotmaihet thangphaet
  • [ISO-abbreviation] J Med Assoc Thai
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Thailand
  • [Number-of-references] 17
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30. Rozeman LB, Hameetman L, Cleton-Jansen AM, Taminiau AH, Hogendoorn PC, Bovée JV: Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas. J Pathol; 2005 Mar;205(4):476-82
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  • Enchondromas and conventional central chondrosarcomas are, respectively, benign and malignant hyaline cartilage-forming tumours that originate in the medulla of bone.
  • In order to gain a better understanding of the molecular process underlying malignant transformation of enchondroma, and to investigate whether there is a biological difference between conventional central cartilaginous tumours and those of enchondromatosis or with phalangeal localization, a series of 64 enchondromas (phalanx, n = 21; enchondromatosis, n = 15) and 89 chondrosarcomas (phalanx, n = 17; enchondromatosis, n = 13) was collected.
  • [MeSH-major] Bone Neoplasms / pathology. Chondrosarcoma / pathology. Enchondromatosis / pathology. Parathyroid Hormone-Related Protein / analysis. Signal Transduction / physiology. Trans-Activators / analysis
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Cell Transformation, Neoplastic / pathology. Child. Child, Preschool. Female. Fingers / pathology. Hedgehog Proteins. Humans. Immunohistochemistry / methods. Male. Middle Aged. Polymerase Chain Reaction / methods. RNA, Messenger / analysis. RNA, Neoplasm / analysis

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  • (PMID = 15685701.001).
  • [ISSN] 0022-3417
  • [Journal-full-title] The Journal of pathology
  • [ISO-abbreviation] J. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Hedgehog Proteins; 0 / Parathyroid Hormone-Related Protein; 0 / RNA, Messenger; 0 / RNA, Neoplasm; 0 / Trans-Activators
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31. Kiralj A, Ilić M, Markov B, Dedić S, Pejaković B, Nalić B: [Chondroma of the skull base and maxilla]. Med Pregl; 2007 Nov-Dec;60(11-12):649-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • INTRODUCTION: Chondromas are uncommon benign tumors of cartilaginous origin.
  • A chondroma is a painless, slow growing tumor causing destruction and exfoliation of teeth.
  • On a radiograph, the tumor appears as a cyst-like radiolucent lesion, while some are sclerotic.
  • DISCUSSION AND CONCLUSION: Chondromyxoid fibroma (CMF) is a rare, benign cartilaginous tumor that often occurs in the metaphyses of proximal tibia, proximal and distal femur and small bones of the foot.
  • The differential diagnosis is wide and includes simple or aneyrismal bone cyst, giant cell tumor, nonossifying fibroma, fibrous dysplasia, enchondroma, chondroblastoma, eosinophilic granuloma and fibrous cortical defect.
  • In the diagnosis of an intracranial chondrocytic tumor, it is important to distinguish it from enchondroma and chondrosarcoma.
  • [MeSH-major] Chondroma. Maxillary Neoplasms. Skull Base Neoplasms

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  • (PMID = 18666612.001).
  • [ISSN] 0025-8105
  • [Journal-full-title] Medicinski pregled
  • [ISO-abbreviation] Med. Pregl.
  • [Language] srp
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Serbia
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32. Hatori M, Watanabe M, Kotake H, Kokubun S: Chondrosarcoma of the ring finger: a case report and review of the literature. Tohoku J Exp Med; 2006 Mar;208(3):275-81
MedlinePlus Health Information. consumer health - Bone Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Enchondromas are the most common benign cartilaginous bone tumors arising in the medullary cavity of the small bones of the hand.
  • The findings of cortical irregular thickening by plain radiography and computed tomography and soft tissue extension by magnetic resonance imaging suggested the tumor was chondrosarcoma rather than a common enchondroma.
  • Histological examination revealed that the tumor was composed of polygonal cells with eosinophilic cytoplasm proliferating in the chondromatous matrix with partially myxoid changes.
  • Nuclear irregularity, binucleated cells, bone permeation and encasement were observed and the tumor was diagnosed as grade 2 chondrosarcoma.
  • The tumor recurred five months after surgery.
  • In conclusion, details of radiological as well as pathological findings are essential for differential diagnosis between benign enchondroma and chondrosarcoma in the hand.
  • [MeSH-major] Bone Neoplasms / pathology. Chondrosarcoma / pathology. Fingers / pathology. Review Literature as Topic
  • [MeSH-minor] Aged, 80 and over. Chondroma / diagnosis. Diagnosis, Differential. Disease-Free Survival. Follow-Up Studies. Humans. Magnetic Resonance Imaging. Male. Neoplasm Recurrence, Local / pathology. Neoplasm Recurrence, Local / surgery. Time Factors. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 16498237.001).
  • [ISSN] 0040-8727
  • [Journal-full-title] The Tohoku journal of experimental medicine
  • [ISO-abbreviation] Tohoku J. Exp. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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33. Budny AM, Ismail A, Osher L: Chondromyxoid fibroma. J Foot Ankle Surg; 2008 Mar-Apr;47(2):153-9
MedlinePlus Health Information. consumer health - Foot Injuries and Disorders.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma is an uncommon benign cartilaginous tumor accounting for less than 1% of all bone tumors.

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  • (PMID = 18312923.001).
  • [ISSN] 1067-2516
  • [Journal-full-title] The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons
  • [ISO-abbreviation] J Foot Ankle Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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34. Romeo S, Duim RA, Bridge JA, Mertens F, de Jong D, Dal Cin P, Wijers-Koster PM, Debiec-Rychter M, Sciot R, Rosenberg AE, Szuhai K, Hogendoorn PC: Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes. Am J Pathol; 2010 Sep;177(3):1365-76
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma (CMF) is an uncommon benign cartilaginous tumor of bone usually occurring during the second decade of life.
  • Two known tumor suppressor genes map to the latter region: PLAGL1 and UTRN.
  • [MeSH-major] Bone Neoplasms / genetics. Chromosome Aberrations. Chromosomes, Human, Pair 6. Fibroma / genetics
  • [MeSH-minor] Cartilage / metabolism. Cartilage / pathology. Cytogenetic Analysis. Humans. Immunohistochemistry. In Situ Hybridization. Polymerase Chain Reaction. Repressor Proteins / genetics. Repressor Proteins / metabolism. Tumor Suppressor Proteins / genetics. Tumor Suppressor Proteins / metabolism. Utrophin / genetics. Utrophin / metabolism

  • MedlinePlus Health Information. consumer health - Bone Cancer.
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  • (PMID = 20696777.001).
  • [ISSN] 1525-2191
  • [Journal-full-title] The American journal of pathology
  • [ISO-abbreviation] Am. J. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / BCLAF1 protein, human; 0 / Repressor Proteins; 0 / Tumor Suppressor Proteins; 0 / Utrophin
  • [Other-IDs] NLM/ PMC2928969
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35. Romeo S, Eyden B, Prins FA, Briaire-de Bruijn IH, Taminiau AH, Hogendoorn PC: TGF-beta1 drives partial myofibroblastic differentiation in chondromyxoid fibroma of bone. J Pathol; 2006 Jan;208(1):26-34
MedlinePlus Health Information. consumer health - Bone Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondromyxoid fibroma (CMF) is a rare benign cartilaginous bone tumour with a lobular architecture containing stellate and myofibroblast-like spindle cells.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology. Transforming Growth Factor beta / metabolism
  • [MeSH-minor] Actins / immunology. Adolescent. Adult. Calcium-Binding Proteins / immunology. Calmodulin-Binding Proteins / immunology. Cell Transformation, Neoplastic. Child. Chondrocytes / pathology. Chondrocytes / ultrastructure. Desmin / immunology. Female. Fibroblasts / pathology. Fibroblasts / ultrastructure. Fibronectins / genetics. Fibronectins / immunology. Genes, Neoplasm / genetics. Humans. Immunohistochemistry / methods. Male. Microfilament Proteins. Microscopy, Electron / methods. Microscopy, Immunoelectron / methods. Middle Aged. Muscle Proteins / immunology. Muscle, Smooth / immunology. Neoplasm Proteins / immunology. Plasminogen Activator Inhibitor 1 / genetics. Plasminogen Activator Inhibitor 1 / immunology. Reverse Transcriptase Polymerase Chain Reaction / methods. Signal Transduction / physiology. Transforming Growth Factor beta1

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  • [Copyright] Copyright 2005 Pathological Society of Great Britain and Ireland.
  • (PMID = 16278817.001).
  • [ISSN] 0022-3417
  • [Journal-full-title] The Journal of pathology
  • [ISO-abbreviation] J. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Actins; 0 / Calcium-Binding Proteins; 0 / Calmodulin-Binding Proteins; 0 / Desmin; 0 / Fibronectins; 0 / Microfilament Proteins; 0 / Muscle Proteins; 0 / Neoplasm Proteins; 0 / Plasminogen Activator Inhibitor 1; 0 / TGFB1 protein, human; 0 / Transforming Growth Factor beta; 0 / Transforming Growth Factor beta1; 0 / calponin
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36. Sheff JS, Wang S: Extraskeletal osteochondroma of the foot. J Foot Ankle Surg; 2005 Jan-Feb;44(1):57-9
MedlinePlus Health Information. consumer health - Foot Injuries and Disorders.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • An extraskeletal osteochondroma is an infrequently encountered benign cartilaginous tumor with a predilection for the hands and feet that usually does not exceed 3 cm in diameter.
  • This diagnosis can be misleading because it bears the same name as the osseous neoplasm more commonly referred to as an exostosis.
  • [MeSH-major] Foot Diseases / pathology. Osteochondroma / pathology. Soft Tissue Neoplasms / pathology

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  • (PMID = 15704084.001).
  • [ISSN] 1067-2516
  • [Journal-full-title] The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons
  • [ISO-abbreviation] J Foot Ankle Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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37. Znati K, Ahaouch M, Fatemi H, Chbani L, Affifi A, Kamaoui I, Bennis S, Amarti A: [Femoral metaphyso-diaphyseal chondroblastoma: a case report]. Rev Chir Orthop Reparatrice Appar Mot; 2007 May;93(3):283-7
Genetic Alliance. consumer health - Chondroblastoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Chondroblastome métaphyso-diaphysaire du fémur: à propos d'un cas.
  • Chondroblastoma is a rare benign tumor of cartilage tissue accounting for less than 1% of all bone tumors.
  • We discuss the anatomic aspects and the clinical course of this rare tumor and present current knowledge of the histogenesis.
  • [MeSH-major] Chondroblastoma / diagnosis. Femoral Neoplasms / diagnosis

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  • (PMID = 17534212.001).
  • [ISSN] 0035-1040
  • [Journal-full-title] Revue de chirurgie orthopédique et réparatrice de l'appareil moteur
  • [ISO-abbreviation] Rev Chir Orthop Reparatrice Appar Mot
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / S100 Proteins; 0 / Vimentin; EC 4.2.1.11 / Phosphopyruvate Hydratase
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38. Bulycheva IV, Semenov LA, Makhson AN, Zhukov AG: [Chondroblastoma]. Arkh Patol; 2007 May-Jun;69(3):53-6
MedlinePlus Health Information. consumer health - Bone Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Chondroblastom, benign cartilage tissue neoplasm, accounts for 1% of all bone tumors.
  • Cartilaginous portions of chondroblastoma form lobular structures.
  • The tumor always comprises single-to-multiple multinucleate giant cells.
  • [MeSH-major] Bone Neoplasms / radiography. Bone Neoplasms / therapy. Chondroblastoma / radiography. Chondroblastoma / therapy

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  • (PMID = 17722601.001).
  • [ISSN] 0004-1955
  • [Journal-full-title] Arkhiv patologii
  • [ISO-abbreviation] Arkh. Patol.
  • [Language] rus
  • [Publication-type] English Abstract; Lectures
  • [Publication-country] Russia (Federation)
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