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Items 1 to 36 of about 36
1. Jonathan A, Rajshekhar V, Chacko G: Chondromyxoid fibroma of the seventh cervical vertebra. Neurol India; 2008 Jan-Mar;56(1):84-7
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  • [Title] Chondromyxoid fibroma of the seventh cervical vertebra.
  • Chondromyxoid fibroma is a rare benign bone tumor representing less than 0.5% of all bone tumors.
  • A presumptive diagnosis of a bony tumor such as an aneurysmal bone cyst or a giant cell tumor involving the seventh vertebral body was made on plain X-rays, MRI and bone scan.
  • He underwent C7 central corpectomy, incomplete intralesional curettage with iliac bone grafting and C6 to T1 interspinous wiring.
  • The histological diagnosis was chondromyxoid fibroma.
  • The authors conclude that corpectomy and iliac bone grafting for chondromyxoid fibroma has a good outcome on long-term follow-up.
  • [MeSH-major] Bone Neoplasms / complications. Bone Neoplasms / pathology. Cervical Vertebrae / pathology. Chondromatosis / complications. Fibroma / complications. Fibroma / pathology

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  • (PMID = 18310848.001).
  • [ISSN] 0028-3886
  • [Journal-full-title] Neurology India
  • [ISO-abbreviation] Neurol India
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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2. Yasuda T, Nishio J, Sumegi J, Kapels KM, Althof PA, Sawyer JR, Reith JD, Bridge JA: Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma. Mod Pathol; 2009 Nov;22(11):1499-506
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  • [Title] Aberrations of 6q13 mapped to the COL12A1 locus in chondromyxoid fibroma.
  • Chondromyxoid fibroma, a rare benign bone tumor, may be mistaken for chondrosarcoma.
  • Although cytogenetic studies of chondromyxoid fibroma are few, rearrangements of the long arm of chromosome 6, frequently expressed as an inv(6)(p25q13), are prominent.
  • In this study, conventional cytogenetic analysis of 16 chondromyxoid fibroma samples from 14 patients revealed rearrangements of chromosome 6 in 10 of 11 clonally abnormal specimens.
  • Notably, an identical t(6;9)(q25;q22) translocation was identified in two cases, suggesting that it represents a distinct translocation of chondromyxoid fibroma.
  • In an effort to further define the aberrant 6q13 breakpoint and identify the molecular consequences, a fluorescence in situ hybridization (FISH)-based positional cloning strategy on chondromyxoid fibroma abnormal metaphase and interphase cells using a series of bacterial and plasmid artificial chromosome (BAC/PAC) probe combinations spanning a 6.1 Mb region was employed.
  • The breakpoint on 6q13 was located within the COL12A1 gene, a collagen gene purportedly involved in another benign bone tumor, subungual exostosis.
  • The findings of this study expand our knowledge of chromosomal alterations in chondromyxoid fibroma, identify COL12A1 as the likely gene candidate within the recurrent 6q13 breakpoint, and provide an alternative approach for detecting 6q13 anomalies in nondividing cells of chondromyxoid fibroma.

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  • (PMID = 19648885.001).
  • [ISSN] 1530-0285
  • [Journal-full-title] Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
  • [ISO-abbreviation] Mod. Pathol.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / CA036727-249009; United States / NCI NIH HHS / CA / P30 CA036727; United States / NCI NIH HHS / CA / P30 CA036727-249009; United States / NCI NIH HHS / CA / P30 CA36727
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / COL12A1 protein, human; 0 / Collagen Type XII; 9007-34-5 / Collagen
  • [Other-IDs] NLM/ NIHMS124998; NLM/ PMC2784180
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3. 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

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  • [Title] Chondromyxoid fibroma of frontal bone: a case report and review of the literature.
  • Chondromyxoid fibroma is an unusual benign tumor of cartilaginous tissues that may be confused with other some malign tumors.
  • Computerized tomography demonstrated a well-defined expansive lesion with a sclerotic margin measuring approximately 3 cm in diameter in the right frontal bone.
  • The histopathological diagnosis was chondromyxoid fibroma.
  • In conclusion, chondromyxoid fibroma is a benign primary bone tumor that is located extremely rarely in the frontal bone.
  • Accurate initial diagnosis of such tumors are important for appropriate 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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4. Romeo S, Oosting J, Rozeman LB, Hameetman L, Taminiau AH, Cleton-Jansen AM, Bovée JV, Hogendoorn PC: The role of noncartilage-specific molecules in differentiation of cartilaginous tumors: lessons from chondroblastoma and chondromyxoid fibroma. Cancer; 2007 Jul 15;110(2):385-94
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  • [Title] The role of noncartilage-specific molecules in differentiation of cartilaginous tumors: lessons from chondroblastoma and chondromyxoid fibroma.
  • BACKGROUND: Chondroblastoma (CB) and chondromyxoid fibroma (CMF) are benign tumors of bone morphologically recapitulating cartilage differentiation.
  • The decreased expression of CCND1, p16INK4A, and CD166 in HGCCS reflects impairment of cell cycle progression and of cell-cell adhesions in malignant tumors and is of use in the differential diagnosis of CMF.
  • [MeSH-major] Bone Neoplasms / metabolism. Chondroblastoma / metabolism. Fibroma / metabolism

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  • (PMID = 17559135.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA Primers
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5. 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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  • [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.
  • Archival paraffin-embedded tissues from 4 fetal femora and 10 cases of chondromyxoid fibroma were analyzed simultaneously using histochemistry (safranin O) and established immunohistochemical antibodies (CD34, CD163, and smooth muscle actin).
  • Similarly, each case of chondromyxoid fibroma demonstrated admixture of two characteristic components: immature fibrous tissue of vascularized stroma with accumulation of macrophages in areas of superficial sinusoidal proliferation, and variable amounts of lobulated chondroid tissue.
  • 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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6. Morris LG, Rihani J, Lebowitz RA, Wang BY: Chondromyxoid fibroma of sphenoid sinus with unusual calcifications: case report with literature review. Head Neck Pathol; 2009 Jun;3(2):169-73
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  • [Title] Chondromyxoid fibroma of sphenoid sinus with unusual calcifications: case report with literature review.
  • Chondromyxoid fibroma (CMF) is a rare benign primary tumor which usually affects the metaphyses of the long bone of the lower extremities in childhood and young adults.
  • [MeSH-minor] Female. Fibroma / pathology. Fibroma / surgery. Humans. Immunohistochemistry. Middle Aged. Tomography, X-Ray Computed

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  • (PMID = 19644549.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 26
  • [Keywords] NOTNLM ; Calcification / Chondromyxoid fibroma / Sphenoid sinus
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7. 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
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  • [Title] TGF-beta1 drives partial myofibroblastic differentiation in chondromyxoid fibroma of bone.
  • 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

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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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8. Bala A, Robbins P, Knuckey N, Wong G, Lee G: Spinal chondromyxoid fibroma of C2. J Clin Neurosci; 2006 Jan;13(1):140-6
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  • [Title] Spinal chondromyxoid fibroma of C2.
  • Chondromyxoid fibroma of bone (CMF) is a rare benign primary bone neoplasm accounting for less than 0.5% of all primary bone neoplasms.
  • The patient underwent stereotactic CT guided trans-oral curettage of the lesion with iliac bone graft and anterior fusion of C2 and C3.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology. Fibroma / pathology. Spinal Neoplasms / pathology

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  • (PMID = 16410218.001).
  • [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; Review
  • [Publication-country] Scotland
  • [Number-of-references] 39
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9. Semenova LA, Bulycheva IV: [Chondromyxoid fibroma]. Arkh Patol; 2007 Mar-Apr;69(2):37-40
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  • [Title] [Chondromyxoid fibroma].
  • Chondromyxoid fibroma is a benign chondroid tissue tumor characterized by the lobular overgrowth of stellate or elongated cells in the myxoid or chondroid intracellular matrix.
  • A positive reaction with S-100 protein, d smooth muscle actin, and CD 34 was immunohistochemically detected in chondromyxoid fibroma tissue.
  • In chondromyxoid fibroma, the prognosis is favorable.
  • [MeSH-major] Bone Neoplasms / diagnosis. Chondroblastoma / diagnosis. Fibroma / diagnosis
  • [MeSH-minor] Bone and Bones / radiography. Bone and Bones / ultrastructure. Humans. Magnetic Resonance Imaging. Tomography, X-Ray Computed

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  • (PMID = 17642191.001).
  • [ISSN] 0004-1955
  • [Journal-full-title] Arkhiv patologii
  • [ISO-abbreviation] Arkh. Patol.
  • [Language] rus
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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10. Budny AM, Ismail A, Osher L: Chondromyxoid fibroma. J Foot Ankle Surg; 2008 Mar-Apr;47(2):153-9
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  • [Title] Chondromyxoid fibroma.
  • Chondromyxoid fibroma is an uncommon benign cartilaginous tumor accounting for less than 1% of all bone tumors.
  • Early detection and complete surgical resection are valuable in preventing recurrence in the affected bone.
  • [MeSH-major] Chondroma / diagnosis. Fibroma / diagnosis. Foot Diseases / diagnosis

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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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11. Ayadi-Kaddour A, Saïji E, Fénniche S, Braham E, Ismail O, Djilani H, El Mezni F: [Costal chondromyxoid fibroma]. Rev Chir Orthop Reparatrice Appar Mot; 2007 Feb;93(1):84-7
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  • [Title] [Costal chondromyxoid fibroma].
  • Chondromyxoid fibroma is a rare benign bone tumor observed in less than 1% of all bone tumors.
  • Pathological diagnosis remains difficult.
  • All bone sites may be involved with a predominance of the metaphysis of long tubular bones, particularly the proximal tibia.
  • We present of case of chondromyxoid fibroma observed in this unusual location in a 31-year-old woman.
  • Local resection was performed and the histological examination showed benign chondromyxoid fibroma.
  • [MeSH-major] Bone Neoplasms / diagnosis. Chondroblastoma / diagnosis. Ribs / pathology

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  • (PMID = 17389829.001).
  • [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
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12. Jhala D, Coventry S, Rao P, Yen F, Siegal GP: Juvenile juxtacortical chondromyxoid fibroma of bone: a case report. Hum Pathol; 2008 Jun;39(6):960-5
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  • [Title] Juvenile juxtacortical chondromyxoid fibroma of bone: a case report.
  • Conventional intramedullary chondromyxoid fibroma (CMF) is a rare benign tumor of bone; juxtacortical lesions are rarer still, and juxtacortical lesions occurring in children are heretofore essentially unreported.
  • Magnetic resonance imaging and bone scan showed changes most consistent with an aggressive biological process.
  • In general, CMF needs to be distinguished from its mimicker low-grade chondrosarcoma, and it must be recognized as occurring on bone surfaces among a wide age range of individuals.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroma / pathology. Fibroma / pathology
  • [MeSH-minor] Child. Chondrosarcoma / diagnosis. Chromosomes, Human, Pair 14. Chromosomes, Human, Pair 21. Chromosomes, Human, Pair 6. Clone Cells. Diagnosis, Differential. Disease-Free Survival. Humans. Magnetic Resonance Imaging. Male. Tibia / pathology. Tibia / surgery. Translocation, Genetic. Treatment Outcome

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  • (PMID = 18400252.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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13. Ebrahimzadeh MH, Dallouei SR: Chondromyxoid fibroma of the calcaneus. J Am Podiatr Med Assoc; 2007 May-Jun;97(3):223-4
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  • [Title] Chondromyxoid fibroma of the calcaneus.
  • Chondromyxoid fibroma is a rare, benign, aggressive bone tumor whose localization in the calcaneus is even rarer.
  • We report a case of chondromyxoid fibroma in the calcaneus of a 10-year-old Iranian boy who was treated with extended curettage.
  • [MeSH-major] Bone Neoplasms / pathology. Calcaneus. Chondroblastoma / pathology. Fibroma / pathology

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  • (PMID = 17507532.001).
  • [ISSN] 8750-7315
  • [Journal-full-title] Journal of the American Podiatric Medical Association
  • [ISO-abbreviation] J Am Podiatr Med Assoc
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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14. Karkuzhali P, Chithralekha S, Muthuvel E, Daniel RB: Chondromyxoid fibroma of the parietal bone. Neuropathology; 2005 Mar;25(1):84-8

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  • [Title] Chondromyxoid fibroma of the parietal bone.
  • We report the case of an 11-year old girl who presented with an intracranial chondromyxoid fibroma arising from parietal bone.
  • Chondromyxoid fibroma is a benign cartilaginous neoplasm, which can be easily mistaken for chondrosarcoma, especially in small biopsies.
  • To our knowledge, this is the second case of chondromyxoid fibroma reported to occur in parietal bone and is the first case reported in an English-language journal.
  • [MeSH-major] Chondroblastoma / pathology. Parietal Bone / pathology. Skull Neoplasms / pathology
  • [MeSH-minor] Child. Diagnosis, Differential. Dura Mater / pathology. Female. Humans. Tomography, X-Ray Computed

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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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15. Bush JB, Sweeney JP, Robison JE, DeMoss B, Meyer MS: Chondromyxoid fibroma of the radial shaft treated with nonvascularized fibular autograft. Am J Orthop (Belle Mead NJ); 2010 Jan;39(1):30-4
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  • [Title] Chondromyxoid fibroma of the radial shaft treated with nonvascularized fibular autograft.
  • Chondromyxoid fibroma is a benign yet highly recurrent neoplasm of bone, usually found in the metaphyseal segments of long bones.
  • We present the case of an unusual diaphyseal chondromyxoid fibroma of the radius and review the literature regarding these rare chondroid neoplasms.
  • [MeSH-major] Bone Neoplasms / pathology. Bone Transplantation / methods. Chondroblastoma / pathology. Fibroma / pathology. Radius / pathology

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  • (PMID = 20305838.001).
  • [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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16. Slotcavage RL, Dickson BC, Ogilvie CM: Chondromyxoid fibroma involving the metacarpophalangeal joint. Orthopedics; 2009 Apr;32(4)
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  • [Title] Chondromyxoid fibroma involving the metacarpophalangeal joint.
  • Chondromyxoid fibroma is a rare benign bony tumor classically occurring in the metaphyseal region of the long bones surrounding the knee, but also found with relative frequency in other long bones, the pelvis, ribs, and small foot bones.
  • We report a case of histopathologically confirmed chondromyxoid fibroma involving a metacarpal, proximal phalanx, and synovial tissues of the metacarpophalangeal joint.
  • Histologic examination revealed an unusual chondromyxoid fibroma with joint involvement.
  • The patient is >15 months out from synovectomy, intralesional curettage, and placement of demineralized bone matrix and allograft cancellous chips, and is without signs of recurrence.
  • This benign, curable lesion should be included in the differential diagnosis of a bony lesion, even when a joint and adjacent bones are involved.
  • [MeSH-major] Bone Neoplasms / radiography. Chondroma / radiography. Fibroma / radiography. Metacarpophalangeal Joint / radiography

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  • (PMID = 19388607.001).
  • [ISSN] 1938-2367
  • [Journal-full-title] Orthopedics
  • [ISO-abbreviation] Orthopedics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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17. 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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  • [Title] Non specific magnetic resonance features of chondromyxoid fibroma of the iliac bone.
  • Chondromyxoid fibroma is a benign cartilaginous neoplasm.
  • The tumor is rare, perhaps the rarest of all bone tumors.
  • We report a case of a 31-year-old woman with chondromyxoid fibroma arising from the iliac bone and presenting with leg pain due to compression on the femoral nerve.
  • Magnetic resonance imaging (MRI) features were non specific for chondromyxoid fibroma.
  • We emphasize the need to consider it in the differential diagnosis of chondrosarcoma.
  • [MeSH-major] Bone Neoplasms / diagnosis. Chondroma / diagnosis. Fibroma / diagnosis. Ilium. Magnetic Resonance Imaging
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Treatment Outcome

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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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18. Vernon SE, Casiano RR: Sphenoid sinus chondromyxoid fibroma mimicking a mucocele. Am J Otolaryngol; 2006 Nov-Dec;27(6):406-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sphenoid sinus chondromyxoid fibroma mimicking a mucocele.
  • We report the case of a 44-year-old man who presented with a chondromyxoid fibroma (CMF) of the sphenoid sinus, which filled the sinus and clinically and radiologically resembled a mucocele.
  • Chondromyxoid fibromas are the least common cartilaginous neoplasms of bone, typically occurring in the metaphysis of long bones.
  • Chondromyxoid fibroma displays a relatively unique histological appearance, with characteristic lobulation, with spindle to stellate cells embedded in a myxoid or chondroid matrix.
  • Although CMFs are generally regarded as benign neoplasms, they may show an infiltrative pattern and may recur, particularly when they are in locations where complete surgical excision may be difficult or impossible.
  • [MeSH-major] Fibroma / diagnosis. Mucocele / pathology. Paranasal Sinus Neoplasms / diagnosis. Sphenoid Sinus / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Male. Tomography, X-Ray Computed

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  • (PMID = 17084225.001).
  • [ISSN] 0196-0709
  • [Journal-full-title] American journal of otolaryngology
  • [ISO-abbreviation] Am J Otolaryngol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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19. 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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  • [Title] Chondromyxoid fibroma resembles in vitro chondrogenesis, but differs in expression of signalling molecules.
  • 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.
  • In chondromyxoid fibroma, specific morphological features correlated with a distinct pattern of expression.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology. Chondrogenesis

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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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20. Lersundi A, Mankin HJ, Mourikis A, Hornicek FJ: Chondromyxoid fibroma: a rarely encountered and puzzling tumor. Clin Orthop Relat Res; 2005 Oct;439:171-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chondromyxoid fibroma: a rarely encountered and puzzling tumor.
  • Chondromyxoid fibroma is an uncommon bone neoplasm, accounting in our series for less than 1% of all connective tissue tumors.
  • The tumor is benign and there have been no reports of metastases.
  • Tumors that were treated with curettage alone did less well than those that were packed with allograft bone or polymethylmethacrylate.
  • The most difficult problem with chondromyxoid fibroma is pathologic identity because it often is confused with more aggressive tumors that may metastasize.
  • [MeSH-major] Bone Neoplasms / pathology. Bone Neoplasms / surgery. Bone Transplantation. Chondroblastoma / pathology. Chondroblastoma / surgery

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  • (PMID = 16205156.001).
  • [ISSN] 0009-921X
  • [Journal-full-title] Clinical orthopaedics and related research
  • [ISO-abbreviation] Clin. Orthop. Relat. Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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21. Fotiadis E, Akritopoulos P, Samoladas E, Akritopoulou K, Kenanidis E: Chondromyxoid fibroma: a rare tumor with an unusual location. Arch Orthop Trauma Surg; 2008 Apr;128(4):371-5
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  • [Title] Chondromyxoid fibroma: a rare tumor with an unusual location.
  • Chondromyxoid fibroma constitutes a rare benign tumor of the bones, which has a potential of regional enlargement towards the local tissues.
  • The differential diagnosis included the chondroblastoma, the aneurysmal cyst and the chondrosarcoma.
  • The biopsy of the tumor confirmed the diagnosis of the chondromyxoid fibroma.
  • [MeSH-major] Bone Neoplasms / diagnosis. Fibroma / diagnosis. Tarsal Bones
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Male. Tomography, X-Ray Computed

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  • (PMID = 17342522.001).
  • [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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22. Murata H, Horie N, Matsui T, Akai T, Ueda H, Oshima Y, Konishi E, Kubo T: Clinical usefulness of thallium-201 scintigraphy and magnetic resonance imaging in the diagnosis of chondromyxoid fibroma. Ann Nucl Med; 2008 Apr;22(3):221-4
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  • [Title] Clinical usefulness of thallium-201 scintigraphy and magnetic resonance imaging in the diagnosis of chondromyxoid fibroma.
  • Chondromyxoid fibroma (CMF) is a benign bone tumor.
  • Contrast-enhanced MR imaging and thallium-201 scintigraphy may be useful to distinguish CMF from benign bone tumors or chondrosarcoma.
  • [MeSH-minor] Adolescent. Biopsy. Citrates / pharmacokinetics. Contrast Media / pharmacokinetics. Diagnosis, Differential. Diphosphonates / pharmacokinetics. Fibroma / radiography. Fibroma / radionuclide imaging. Fibula / pathology. Gadolinium DTPA / pharmacokinetics. Gallium / pharmacokinetics. Humans. Knee Joint / pathology. Knee Joint / radiography. Knee Joint / radionuclide imaging. Knee Joint / surgery. Magnetic Resonance Imaging. Male. Osteolysis / radiography. Radionuclide Imaging. Radiopharmaceuticals / pharmacokinetics. Technetium Compounds / pharmacokinetics

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  • (PMID = 18498038.001).
  • [ISSN] 0914-7187
  • [Journal-full-title] Annals of nuclear medicine
  • [ISO-abbreviation] Ann Nucl Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Citrates; 0 / Contrast Media; 0 / Diphosphonates; 0 / Radiopharmaceuticals; 0 / Technetium Compounds; 0 / Thallium Radioisotopes; 27905-02-8 / gallium citrate; 8V3FGC4J77 / technetium Tc 99m diphosphonate; CH46OC8YV4 / Gallium; K2I13DR72L / Gadolinium DTPA
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23. Daghfous M, Charfi H, Turki M, Maalla R, Baccari S, Tarhouni L: [Chondromyxoid fibroma. A case report of location in the phalanx of the thumb]. Chir Main; 2007 Jun;26(3):159-64
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  • [Title] [Chondromyxoid fibroma. A case report of location in the phalanx of the thumb].
  • Chondromyxoid Fibroma is a rare benign osseous tumor especially in the hand, because the hand represents less than 3% of all osseous locations.
  • It can causes problems of differential diagnosis with several types of tumors and in particular with chondrosarcoma, for which the management is totally different.
  • We report a case of location of a chondromyxoid fibroma in a phalanx of the thumb, which caused problems of differential diagnosis with chondroma and chondrosarcoma.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology. Fibroma / pathology. Thumb / pathology

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  • (PMID = 17590372.001).
  • [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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24. 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
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  • [Title] Heterogeneous and complex rearrangements of chromosome arm 6q in chondromyxoid fibroma: delineation of breakpoints and analysis of candidate target genes.
  • Chondromyxoid fibroma (CMF) is an uncommon benign cartilaginous tumor of bone usually occurring during the second decade of life.
  • [MeSH-major] Bone Neoplasms / genetics. Chromosome Aberrations. Chromosomes, Human, Pair 6. Fibroma / genetics

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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
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25. Feuvret L, Noël G, Calugaru V, Terrier P, Habrand JL: Chondromyxoid fibroma of the skull base: differential diagnosis and radiotherapy: two case reports and a review of the literature. Acta Oncol; 2005;44(6):545-53

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chondromyxoid fibroma of the skull base: differential diagnosis and radiotherapy: two case reports and a review of the literature.
  • Chondromyxoid fibromas are uncommon tumours mostly arising in long bones of young males.
  • We describe two new cases of base of the skull chondromyxoid fibromas.
  • Skull base chondromyxoid fibroma is a very rare, slowly growing benign tumour that can cause severe disabilities due to tumour compression of critical structures.
  • Our review of the literature allows us to conclude that histological diagnosis of lesions in this site is a trap for pathologists and that radiotherapy is not contraindicated.
  • [MeSH-major] Chondroblastoma / diagnosis. Chondroblastoma / radiotherapy. Skull Base Neoplasms / diagnosis. Skull Base Neoplasms / radiotherapy
  • [MeSH-minor] Adolescent. Adult. Aged. Bone Neoplasms / diagnosis. Bone Neoplasms / radiotherapy. Bone Neoplasms / surgery. Cell Transformation, Neoplastic. Diagnosis, Differential. Diplopia / etiology. Female. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Paresthesia / etiology. Radiation Dosage

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  • (PMID = 16165913.001).
  • [ISSN] 0284-186X
  • [Journal-full-title] Acta oncologica (Stockholm, Sweden)
  • [ISO-abbreviation] Acta Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Norway
  • [Number-of-references] 45
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26. Armah HB, McGough RL, Goodman MA, Gollin SM, Surti U, Parwani AV, Rao UN: Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites. Diagn Pathol; 2007;2:44
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  • [Title] Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites.
  • BACKGROUND: Chondromyxoid fibromas (CMFs) are rare benign chondroid/myxoid matrix-producing tumors that occur in metaphyses of long tubular bones, and very rarely in small bones of hands and feet.
  • Flat bone involvement is even more uncommon.
  • CONCLUSION: CMF originating in unusual locations should be distinguished from chondrosarcomas, especially on small biopsies, and should be included in the differential diagnosis.

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  • (PMID = 18036245.001).
  • [ISSN] 1746-1596
  • [Journal-full-title] Diagnostic pathology
  • [ISO-abbreviation] Diagn Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2203974
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27. Desai SS, Jambhekar NA, Samanthray S, Merchant NH, Puri A, Agarwal M: Chondromyxoid fibromas: a study of 10 cases. J Surg Oncol; 2005 Jan 1;89(1):28-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chondromyxoid fibromas: a study of 10 cases.
  • Chondromyxoid fibroma (CMF) can be confused with a malignant tumor because of its potential for recurrence and occasional nuclear atypia.
  • The histology showed lobulated chondromyxoid matrix with peripheral fibrosis.
  • The study emphasizes that despite nuclear atypia and recurrences, CMF is a benign disease.
  • [MeSH-major] Bone Neoplasms / pathology. Chondroblastoma / pathology

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  • (PMID = 15612014.001).
  • [ISSN] 0022-4790
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 15
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28. Konishi E, Nakashima Y, Iwasa Y, Nakao R, Yanagisawa A: Immunohistochemical analysis for Sox9 reveals the cartilaginous character of chondroblastoma and chondromyxoid fibroma of the bone. Hum Pathol; 2010 Feb;41(2):208-13
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Immunohistochemical analysis for Sox9 reveals the cartilaginous character of chondroblastoma and chondromyxoid fibroma of the bone.
  • Chondroblastoma, which is histologically composed of mononuclear cell proliferation and lobules of immature cartilage, and chondromyxoid fibroma, which is composed of myxoid lobules with spindle or stellate cells and a cellular fibrous rim with spindle cells, are both rare tumors.
  • Based on histogenetic investigation including immunohistochemistry, matrix biochemistry, and electron microscopy, chondroblastoma is thought to contain chondrogenic cells, whereas chondromyxoid fibroma is considered to contain myofibroblastic cells, as well as chondrogenic cells, and chondroid matrix.
  • In this study, we performed immunohistochemical analysis for Sox9, which is an essential transcriptional factor for chondrogenesis, to examine the possible chondrogenic nature of chondroblastoma and chondromyxoid fibroma.
  • Formalin-fixed, paraffin-embedded tissues obtained from 10 cases of chondroblastoma and 11 cases of chondromyxoid fibroma were immunostained with antibody to Sox9.
  • Sox9 was positive in 8 chondroblastomas and 10 chondromyxoid fibromas.
  • The matrices of 7 chondroblastomas and of 8 chondromyxoid fibromas were immunopositive for collagen type II.
  • The findings suggest the cartilaginous differentiation of chondroblastoma and chondromyxoid fibroma.
  • [MeSH-major] Bone Neoplasms / metabolism. Bone and Bones / metabolism. Cartilage / metabolism. Chondroblastoma / metabolism. Fibroma / metabolism. SOX9 Transcription Factor / metabolism

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  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
  • (PMID = 19801163.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Collagen Type II; 0 / SOX9 Transcription Factor
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29. Romeo S, Hogendoorn PC, Dei Tos AP: Benign cartilaginous tumors of bone: from morphology to somatic and germ-line genetics. Adv Anat Pathol; 2009 Sep;16(5):307-15
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Benign cartilaginous tumors of bone: from morphology to somatic and germ-line genetics.
  • Benign cartilaginous tumors of bones, intrinsic to their name, are tumors forming cartilaginous matrix with a clinically benign behavior.
  • In this group, we recognize osteochondromas, (en)chondromas, chondroblastomas, and chondromyxoid fibromas.
  • This group includes common tumors, that is, osteochondroma and (en)chondroma as well as rare tumors such as chondroblastoma and chondromyxoid fibroma.
  • Several benign and malignant tumors may mimic benign cartilaginous tumors of bones.
  • We reviewed the main morphologic features and the differential diagnosis is discussed.
  • [MeSH-major] Bone Neoplasms / genetics. Bone Neoplasms / pathology. Cartilage / pathology
  • [MeSH-minor] Adolescent. Adult. Child. Chondroblastoma / genetics. Chondroblastoma / pathology. Chondroma / genetics. Chondroma / pathology. Diagnosis, Differential. Female. Fibroma / genetics. Fibroma / pathology. Germ-Line Mutation. Humans. Immunohistochemistry. Male. Membrane Proteins / analysis. Membrane Proteins / genetics. Membrane Proteins / metabolism. Middle Aged. N-Acetylglucosaminyltransferases / analysis. N-Acetylglucosaminyltransferases / genetics. N-Acetylglucosaminyltransferases / metabolism. Osteochondroma / genetics. Osteochondroma / pathology. Translocation, Genetic

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  • (PMID = 19700940.001).
  • [ISSN] 1533-4031
  • [Journal-full-title] Advances in anatomic pathology
  • [ISO-abbreviation] Adv Anat Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Membrane Proteins; EC 2.4.1.- / EXTL2 protein, human; EC 2.4.1.- / N-Acetylglucosaminyltransferases
  • [Number-of-references] 94
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30. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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.
  • [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.
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  • (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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31. Chen WL, Ye JT, Yang ZH, Huang ZQ, Zhang DM, Wang K: Reverse facial artery-submental artery mandibular osteomuscular flap for the reconstruction of maxillary defects following the removal of benign tumors. Head Neck; 2009 Jun;31(6):725-31
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Reverse facial artery-submental artery mandibular osteomuscular flap for the reconstruction of maxillary defects following the removal of benign tumors.
  • METHODS: Eight maxillary defects following benign tumor ablation were repaired with reverse facial artery-submental artery mandibular osteomuscular flaps.
  • Maxillary odontogenic myxoma was present in 3 cases, maxillary fibrous dysplasia and ameloblastoma in 2 cases each, and chondromyxoid fibroma in 1 case.
  • [MeSH-minor] Adolescent. Adult. Bone Transplantation / methods. Esthetics. Female. Follow-Up Studies. Graft Survival. Humans. Male. Mandible / transplantation. Retrospective Studies. Risk Assessment. Treatment Outcome. Wound Healing / physiology. Young Adult

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  • [Copyright] (c) 2009 Wiley Periodicals, Inc.
  • (PMID = 19260126.001).
  • [ISSN] 1097-0347
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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32. 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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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [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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33. Jarkiewicz-Kochman E, Gołebiowski M, Swiatkowski J, Pacholec E, Rajewski R: Tumours of the metatarsus. Ortop Traumatol Rehabil; 2007 May-Jun;9(3):319-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Single cases of the following tumours have been discussed: giant cell tumour, metastases (lung, prostate gland), chondroblastoma, aneurysmal bone cyst, Ewing's sarcoma, clear cell carcinoma, osteosarcoma, intraosseous ganglion, chondromyxoid fibroma and granuloma.
  • The aim of the present study was to carry out a systematic examination of metatarsal tumours with regard to methods of diagnosis (location) and morphology.
  • RESULTS: Most of the metatarsal tumours were benign.
  • Bone tumours are rarely located in the metatarsus.
  • 4. The frequently unequivocal presentation of metatarsal tumours requires a multidisciplinary diagnosis involving a clinician, a radiologist and a histopathologist.
  • [MeSH-major] Bone Neoplasms / diagnosis. Metatarsal Bones / radiography
  • [MeSH-minor] Adult. Bone Cysts, Aneurysmal / diagnosis. Diagnosis, Differential. Female. Giant Cell Tumor of Bone / diagnosis. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Osteochondroma / diagnosis. Osteoma / diagnosis. Sarcoma, Synovial / diagnosis. Soft Tissue Neoplasms / diagnosis. Tomography, X-Ray Computed

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  • (PMID = 17721430.001).
  • [ISSN] 1509-3492
  • [Journal-full-title] Ortopedia, traumatologia, rehabilitacja
  • [ISO-abbreviation] Ortop Traumatol Rehabil
  • [Language] eng; pol
  • [Publication-type] Journal Article
  • [Publication-country] Poland
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34. Baker AC, Rezeanu L, O'Laughlin S, Unni K, Klein MJ, Siegal GP: Juxtacortical chondromyxoid fibroma of bone: a unique variant: a case study of 20 patients. Am J Surg Pathol; 2007 Nov;31(11):1662-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juxtacortical chondromyxoid fibroma of bone: a unique variant: a case study of 20 patients.
  • BACKGROUND: Chondromyxoid fibroma (CMF) is a rare neoplasm of the appendicular skeleton of young adults.
  • This entity should be included in the differential diagnosis of bone surface lesions as it may be mistaken for a more aggressive neoplasm.
  • The most common presentation was bone pain.
  • CONCLUSION: CMF should be included in the differential diagnosis of bone surface lesions.
  • [MeSH-major] Bone Neoplasms / pathology. Bone and Bones / pathology. Calcinosis / pathology. Fibroma / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Magnetic Resonance Imaging. Male. Middle Aged. Pain / etiology. Prognosis. Retrospective Studies. Tomography, X-Ray Computed. United States

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  • (PMID = 18059222.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Multicenter Study
  • [Publication-country] United States
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35. Delling G, Jobke B, Burisch S, Werner M: [Cartilage tumors. Classification, conditions for biopsy and histologic characteristics]. Orthopade; 2005 Dec;34(12):1267-81; quiz 1281-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Primary cartilage-forming tumors of the bone are a large group among the rare bone tumors.
  • Bone biopsy is still the most relevant examination in the final diagnosis of the lesion.
  • Differentiation between benign enchondroma and grade I chondrosarcoma requires close interdisciplinary cooperation to avoid over-treatment and relapse.
  • The same applies to benign entities such as osteochondroma, chondroblastoma and chondromyxoid fibroma.
  • [MeSH-major] Biopsy / methods. Bone Neoplasms / classification. Bone Neoplasms / pathology. Cartilage / pathology. Neoplasms, Connective Tissue / classification. Neoplasms, Connective Tissue / pathology
  • [MeSH-minor] Diagnosis, Differential. Humans. Practice Guidelines as Topic. Practice Patterns, Physicians'

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  • (PMID = 16322881.001).
  • [ISSN] 0085-4530
  • [Journal-full-title] Der Orthopäde
  • [ISO-abbreviation] Orthopade
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 30
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36. 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.
  • 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.
  • MR provides a detailed assessment of soft tissue masses of the craniofacial region, while CT offers superior analysis of bone structure involvement.
  • The present case underlines the importance of MR examination in the diagnosis of soft tissue masses in the craniofacial region.

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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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