Angiofibroma of soft tissue with fibrohistiocytic features and intratumor genetic heterogeneity of NCOA2 gene rearrangement revealed by chromogenic in situ hybridization: A case report. (May 2014)
- Record Type:
- Journal Article
- Title:
- Angiofibroma of soft tissue with fibrohistiocytic features and intratumor genetic heterogeneity of NCOA2 gene rearrangement revealed by chromogenic in situ hybridization: A case report. (May 2014)
- Main Title:
- Angiofibroma of soft tissue with fibrohistiocytic features and intratumor genetic heterogeneity of NCOA2 gene rearrangement revealed by chromogenic in situ hybridization: A case report
- Authors:
- Fukuda, Yumiko
Motoi, Toru
Kato, Ikuma
Ikegami, Masachika
Funata, Nobuaki
Ohtomo, Rie
Horiguchi, Shinichiro
Goto, Takahiro
Hishima, Tsunekazu - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Angiofibroma of soft tissue is a recently described soft tissue tumor that is characterized by fibroblastic spindle tumor cells with arborizing capillary proliferation. Cytogenetically, it harbors a specific fusion gene involving the nuclear receptor coactivator 2 (<italic>NCOA2</italic>) gene. We report here additional new pathological and cytogenetic features. A soft tissue tumor in the left thigh of 73‐year‐old female was investigated. Microscopically, histiocytoid tumor cells were scattered in an edematous background with branching capillary proliferation. Immunohistochemically, we identified that the tumor cells were positive for histiocytic markers such as CD68 and CD163. Rearrangement of the <italic>NCOA2</italic> gene was detected successfully by chromogenic <italic>in situ</italic> hybridization; however, abnormal signal patterns were observed in only a small subset of tumor cells. Unlike typical tumors with bland spindle cells, the present tumor needs to be distinguished from myxoid, dendritic and clear cell tumors. This case may suggest that angiofibroma of soft tissue is not in the center of the fibroblastic/myofibroblastic tumor group, but rather shows a fibrohistiocytic nature. We also found intratumor genetic heterogeneity, which is uncommon for a translocation‐associated tumor. Therefore, careful evaluation is required to detect the gene rearrangement in this tumor<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Angiofibroma of soft tissue is a recently described soft tissue tumor that is characterized by fibroblastic spindle tumor cells with arborizing capillary proliferation. Cytogenetically, it harbors a specific fusion gene involving the nuclear receptor coactivator 2 (<italic>NCOA2</italic>) gene. We report here additional new pathological and cytogenetic features. A soft tissue tumor in the left thigh of 73‐year‐old female was investigated. Microscopically, histiocytoid tumor cells were scattered in an edematous background with branching capillary proliferation. Immunohistochemically, we identified that the tumor cells were positive for histiocytic markers such as CD68 and CD163. Rearrangement of the <italic>NCOA2</italic> gene was detected successfully by chromogenic <italic>in situ</italic> hybridization; however, abnormal signal patterns were observed in only a small subset of tumor cells. Unlike typical tumors with bland spindle cells, the present tumor needs to be distinguished from myxoid, dendritic and clear cell tumors. This case may suggest that angiofibroma of soft tissue is not in the center of the fibroblastic/myofibroblastic tumor group, but rather shows a fibrohistiocytic nature. We also found intratumor genetic heterogeneity, which is uncommon for a translocation‐associated tumor. Therefore, careful evaluation is required to detect the gene rearrangement in this tumor entity.</p> </abstract> … (more)
- Is Part Of:
- Pathology international. Volume 64:Number 5(2014:May)
- Journal:
- Pathology international
- Issue:
- Volume 64:Number 5(2014:May)
- Issue Display:
- Volume 64, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 64
- Issue:
- 5
- Issue Sort Value:
- 2014-0064-0005-0000
- Page Start:
- 237
- Page End:
- 242
- Publication Date:
- 2014-05
- Subjects:
- Pathology -- Periodicals
616.07 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=pin ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/pin.12163 ↗
- Languages:
- English
- ISSNs:
- 1320-5463
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6412.823000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3998.xml