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Claudin-1 is expressed in perineurioma-like low-grade fibromyxoid sarcoma.

Authors :
Thway, Khin
Fisher, Cyril
Debiec-Rychter, Maria
Calonje, Eduardo
Source :
Human Pathology; Nov2009, Vol. 40 Issue 11, p1586-1590, 5p
Publication Year :
2009

Abstract

Summary: Low-grade fibromyxoid sarcoma is a soft tissue sarcoma with recurrent and low metastatic potential, which has characteristic FUS-CREB3L2 or FUS-CREB3L1 fusions. Perineurioma is a peripheral nerve sheath neoplasm, which is usually benign. Low-grade fibromyxoid sarcoma and perineurioma can appear morphologically similar, particularly in small biopsy specimens, and distinction between the 2 entities is important for appropriate treatment. Low-grade fibromyxoid sarcoma is negative for most immunohistochemical markers, whereas perineuriomas stain variably for epithelial membrane antigen, CD34 and claudin-1, a tight-junction associated protein. We studied 15 cases of genetically proven low-grade fibromyxoid sarcoma that at least focally resembled perineurioma, with antibodies to claudin-1 and epithelial membrane antigen. Of these, 11 showed positivity for epithelial membrane antigen and all 15 were positive for claudin-1; in all cases, expression of claudin-1 was equal to or greater than the corresponding epithelial membrane antigen expression. This study emphasizes that claudin-1 is significantly expressed in low-grade fibromyxoid sarcomas. This has implications toward the accurate diagnosis of both tumors, and, as positivity for claudin-1 in low-grade fibromyxoid sarcoma is not previously documented, suggests that there might be underdiagnosis of low-grade fibromyxoid sarcoma. Although positivity for claudin-1 remains useful as an adjunct marker for perineurioma, it should be taken in context with clinical findings, morphology, and the additional immunoprofile. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00468177
Volume :
40
Issue :
11
Database :
Supplemental Index
Journal :
Human Pathology
Publication Type :
Academic Journal
Accession number :
44700985
Full Text :
https://doi.org/10.1016/j.humpath.2009.04.003