Phenotypic variation in different lesions of mycosis fungoides biopsied within a short period of time from the same patient Journal Article


Authors: Kash, N.; Massone, C.; Fink-Puches, R.; Cerroni, L.
Article Title: Phenotypic variation in different lesions of mycosis fungoides biopsied within a short period of time from the same patient
Abstract: Phenotypic variants of mycosis fungoides (MF) include mainly the expression of cytotoxic markers by neoplastic cells (either alpha/beta or gamma/delta cytotoxic). To manage the patient properly, distinction from other cutaneous cytotoxic natural killer/T-cell lymphomas is paramount. Particularly for cutaneous gamma/delta T-cell lymphoma, distinction is often based on clinicopathologic correlation (presence of tumors at first diagnosis as opposed to patches only in MF). The authors report a case of cytotoxic MF characterized by expression of TCR gamma in two of three biopsies performed within a time frame of 1 week. The patient presented with patches, plaques, and 1 tumor at the time of first diagnosis; thus, distinction from cutaneous gamma/delta T-cell lymphoma was not possible on clinical grounds alone. The diagnosis of MF was established, thanks to the phenotypic variations revealed by the three biopsies, with 1 lacking expression of cytotoxic proteins (TIA-1 and granzyme B) and of TCR gamma. This case shows the importance to perform several biopsies in cases of cutaneous lymphoma, as morphologic and phenotypic features are variable and information gathered from a single biopsy may result in a wrong diagnosis.
Keywords: cutaneous; lymphoma; cytotoxic; t-cell lymphoma; phenotypic variation; mycosis fungoides; expression; heterogeneity; clinical behavior; of-the-literature; immunophenotype; gamma-delta; t-cell lymphomas; cutaneous gamma-delta t-cell lymphoma
Journal Title: American Journal of Dermatopathology
Volume: 38
Issue: 7
ISSN: 0193-1091
Publisher: Lippincott Williams & Wilkins  
Date Published: 2016-07-01
Start Page: 541
End Page: 545
Language: English
ACCESSION: WOS:000378157800016
PROVIDER: wos
PUBMED: 26885605
DOI: 10.1097/DAD.0000000000000493
Notes: Article -- Source: Wos
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  1. Natalie Nata Kash
    1 Kash