A Literature Revision in Primary Cutaneous B-cell Lymphoma.

Autor: Selva R; Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy., Violetti SA; UOC Dermatologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy., Delfino C; Department of Surgery and Translational Medicine, Section of Dermatology and Venereology, University of Florence Medical School, Florence, Italy., Grandi V; Department of Surgery and Translational Medicine, Section of Dermatology and Venereology, University of Florence Medical School, Florence, Italy., Cicchelli S; Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy., Tomasini C; Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy., Fierro MT; Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy., Berti E; University of Milano-Bicocca, Milan, Italy., Pimpinelli N; Department of Surgery and Translational Medicine, Section of Dermatology and Venereology, University of Florence Medical School, Florence, Italy., Quaglino P; Department of Medical Sciences, Dermatologic Clinic, University of Turin, Turin, Italy.
Jazyk: angličtina
Zdroj: Indian journal of dermatology [Indian J Dermatol] 2017 Mar-Apr; Vol. 62 (2), pp. 146-157.
DOI: 10.4103/ijd.IJD_74_17
Abstrakt: The term "Primary Cutaneous B-Cell Lymphoma" (PCBCL) comprehends a variety of lymphoproliferative disorders characterized by a clonal proliferation of B-cells primarily involving the skin. The absence of evident extra-cutaneous disease must be confirmed after six-month follow-up in order to exclude a nodal non-Hodgkin's lymphoma (NHL) with secondary cutaneous involvement, which may have a completely different clinical behavior and prognosis. In this article, we have summarized the clinico-pathological features of main types of PCBCL and we outline the guidelines for management based on a review of the available literature.
Competing Interests: There are no conflicts of interest. What is new? Through a review of the available literature, we have highlighted the unique clinical and histological characteristics of the main CBCL, we have underlined their prognosis and we have summarized the diagnostic approach and the therapeutic management.
Databáze: MEDLINE
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