Long‐term follow‐up and management of small and medium‐sized CD4+ T cell lymphoma and CD8+ lymphoid proliferations of acral sites: a multicenter experience
International Journal of Dermatology2016Vol. 55(11), pp. 1248–1254
Citations Over TimeTop 10% of 2016 papers
Pooja Virmani, Sarah I. Jawed, Patricia L. Myskowski, Sarah McCue Horwitz, Anna Lucas, Alison J. Moskowitz, Melissa Pulitzer, Jasmine Zain, Steven T. Rosen, Christiane Querfeld
Abstract
The CD4+ SMPTCL/CD8+ LP subgroup usually presents with solitary lesions and demonstrates an indolent clinical course. Typical presentation, classic histopathology, widespread expression of follicular T helper cell markers, and loss of a T cell antigen are diagnostic features of CD4+ SMPTCL, whereas monomorphous CD8+ infiltrate without follicular T helper cell markers is consistent with CD8+ LP. Local skin-directed therapy is appropriate in these patients.
Related Papers
- → Follicular lymphoma-like B cells of uncertain significance (in situ follicular lymphoma) may infrequently progress, but precedes follicular lymphoma, is associated with other overt lymphomas and mimics follicular lymphoma in flow cytometric studies(2013)65 cited
- → An Atypical relapsing follicular lymphoma to composite Hodgkin’s lymphoma(2023)2 cited
- → Dissecting the gray zone between follicular lymphoma and marginal zone lymphoma using morphological and genetic features(2013)15 cited
- → Molecular and immunohistochemical characterization of B-cell lymphoma-2–negative follicular lymphomas(2011)9 cited
- Comparative analysis of histopathological alterations and immunohistochemistry in cattle for diagnosis of rabies(2013)