Primär kutanes peripheres T-Zell-Lymphom (nicht anderweitig spezifiziert) View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-05

AUTHORS

C. Mühlhoff, N. Gaßler, M. Megahed

ABSTRACT

Peripheral cutaneous T-cell lymphoma which cannot be further classified due to high morphological and molecular variability are included into the group of "primary cutaneous peripheral T-cell lymphoma--not otherwise specified" (PCTL-NOS). PCTL-NOS represent a rare, heterogeneous group characterized by rapidly progressive nodules in the absence of typical mycosis fungoides plaques. Furthermore, therapeutic options are limited and prognosis is rather poor. We report on a 62-year-old patient presenting with asymptomatic papules in the popliteal and antecubital fossae. Based on histopathological criteria, PCTL-NOS was diagnosed. Based on recent gene expression studies, a positive reaction to tyrosine kinase and histone deacetylase inhibitors is hoped for. More... »

PAGES

332-335

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00105-011-2164-3

DOI

http://dx.doi.org/10.1007/s00105-011-2164-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030293137

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21437704


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