Literature DB >> 9870143

Utility of cytokeratin subsets for distinguishing poorly differentiated synovial sarcoma from peripheral primitive neuroectodermal tumour.

S K Machen1, C Fisher, R S Gautam, R R Tubbs, J R Goldblum.   

Abstract

AIMS: Poorly differentiated synovial sarcoma (PDSS) is a round cell sarcoma that may be difficult to distinguish from other round cell sarcomas, such as peripheral primitive neuroectodermal tumour (pPNET), on histological examination alone. Furthermore, these two tumours may show overlapping immunophenotypes, as some cases of PDSS express CD99, and, on the other hand, pPNET may express epithelial markers. The goal of this study was to determine the utility of cytokeratin (CK) subsets in distinguishing between these two lesions. METHODS AND
RESULTS: We evaluated 13 cases of pPNET with RT-PCR detected EWS/FLI-1 fusion transcript and 21 cases of PDSS for the immunohistochemical expression of CK7 and CK19. All cases of PDSS had areas of recognizable monophasic or biphasic synovial sarcoma that expressed at least one epithelial marker. Thirteen of 21 (62%) PDSS stained with AE1/AE3. CK7 and 19 were expressed in 11 (52%) and nine (43%) cases, respectively. Although six of 19 (32%) PDSS demonstrated cytoplasmic staining for CD99, none showed a membranous pattern of immunoreactivity. In contrast, 12 of 13 (92%) pPNET showed strong membranous immunoreactivity for CD99. Four tumours (31%) showed focal staining with AE1/AE3, two of which (15%) stained for CK19. CK7 was not detected in any of the pPNETs.
CONCLUSIONS: Although AE1/AE3 may be found in up to 31% of cases of pPNET, the expression of CK7 makes this diagnosis less likely.

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Year:  1998        PMID: 9870143     DOI: 10.1046/j.1365-2559.1998.00562.x

Source DB:  PubMed          Journal:  Histopathology        ISSN: 0309-0167            Impact factor:   5.087


  7 in total

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Authors:  Ursula Úrias; Suely K N Marie; Miyuki Uno; Roseli da Silva; Mariá M Evagelinellis; Otavia L Caballero; Brian J Stevenson; Wilson A Silva; Andrew J Simpson; Sueli M Oba-Shinjo
Journal:  J Neurooncol       Date:  2014-05-06       Impact factor: 4.130

2.  Solitary primary pulmonary synovial sarcoma: A case report.

Authors:  Wei-Wei He; Zhi-Xin Huang; Wen-Jing Wang; Yu-Lei Li; Qiu-Yuan Xia; Yong-Bin Qiu; Yi Shi; Hui-Ming Sun
Journal:  World J Clin Cases       Date:  2022-05-26       Impact factor: 1.534

3.  A practical and comprehensive immunohistochemical approach to the diagnosis of superficial soft tissue tumors.

Authors:  Wael Al-Daraji; Ehab Husain; Bettena G Zelger; Bernhard Zelger
Journal:  Int J Clin Exp Pathol       Date:  2008-06-10

Review 4.  Soft tissue sarcomas with non-EWS translocations: molecular genetic features and pathologic and clinical correlations.

Authors:  Cyril Fisher
Journal:  Virchows Arch       Date:  2009-04-28       Impact factor: 4.064

5.  Usefulness of a monoclonal ERG/FLI1 antibody for immunohistochemical discrimination of Ewing family tumors.

Authors:  Scott A Tomlins; Nallasivam Palanisamy; J Chad Brenner; Jennifer N Stall; Javed Siddiqui; Dafydd G Thomas; David R Lucas; Arul M Chinnaiyan; Lakshmi P Kunju
Journal:  Am J Clin Pathol       Date:  2013-06       Impact factor: 2.493

6.  Malignant primary intraosseus synovial sarcoma - a rare case report.

Authors:  Kingsley Iyoko Iseko; Solomon M Awoyemi; Meraiyebu Aminyene Essien; Akafa Tensaba; Nkechi Gift Inyang; Josephine Bosede Iseko; Friday Olah
Journal:  Radiol Case Rep       Date:  2021-12-03

7.  Immunohistochemical validation of TLE1, a novel marker, for synovial sarcomas.

Authors:  Bharat Rekhi; Ranjan Basak; Sangeeta B Desai; Nirmala A Jambhekar
Journal:  Indian J Med Res       Date:  2012-11       Impact factor: 2.375

  7 in total

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