Tenosynovial Giant Cell Tumor, Localized Type With Extensive Chondroid Metaplasia: A Case Report With Immunohistochemical and Molecular Genetic Analysis

International Journal of Surgical Pathology Volume 28 Issue 4 Page 447-453 published_at 2019-11-26
アクセス数 : 1633
ダウンロード数 : 205

今月のアクセス数 : 56
今月のダウンロード数 : 6
File
Title
Tenosynovial Giant Cell Tumor, Localized Type With Extensive Chondroid Metaplasia: A Case Report With Immunohistochemical and Molecular Genetic Analysis
Creator
Nagano Nahoko
Fujimoto Makiko
Biyajima Kyoko
Source Title
International Journal of Surgical Pathology
Volume 28
Issue 4
Start Page 447
End Page 453
Journal Identifire
ISSN 1066-8969
EISSN 1940-2465
Descriptions
Tenosynovial giant cell tumor (TSGCT) of localized type is a common disease occurring mostly in the hands. Diagnosis of this tumor is relatively easy to render with hematoxylin-eosin–stained sections as compared with that of TSGCT of diffuse type. However, very rare cases with chondroid metaplasia that have recently been reported mainly in diffuse type can make pathological differentiation from soft tissue cartilaginous tumors extremely difficult. In this article, the authors present the second reported case of TSGCT of localized type showing extensive chondroid metaplasia. Pathological interpretation was difficult without utilizing immunohistochemistry and fluorescence in situ hybridization. One must be careful not to misdiagnose this lesion as cartilaginous tumors of soft tissue, and we suspect at least some chondroblastoma-like chondroma could be reclassified as TSGCT of localized type with extensive chondroid metaplasia. Morphological, immunohistochemical, and molecular genetic characteristics are presented and discussed.
Subjects
tenosynovial giant cell tumor ( Other)
localized type ( Other)
chondroid metaplasia, clusterin ( Other)
COL6A3-CSF1 fusion gene ( Other)
Language
eng
Resource Type journal article
Publisher
SAGE
Date of Issued 2019-11-26
Publish Type Accepted Manuscript
Access Rights open access
Relation
[DOI] 10.1177/1066896919889672
[URI] https://journals.sagepub.com/home/ijs
[PMID] 31771368