Cutaneous pseudolymphoma-A review on the spectrum and a proposal for a new classification

被引:73
|
作者
Mitteldorf, Christina [1 ]
Kempf, Werner [2 ,3 ]
机构
[1] Univ Med Ctr, Dept Dermatol Venereol & Allergol, Robert Koch Str 40, D-37075 Gottingen, Germany
[2] Kempf & Pfaltz Histolog Diagnost, Zurich, Switzerland
[3] Univ Hosp Zurich, Dept Dermatol, Zurich, Switzerland
关键词
B-cell lymphoma; Borreliosis; clonality; cutaneous pseudolymphoma; infection; T-cell lymphoma; tattoo; B-CELL LYMPHOMA; MARGINAL ZONE LYMPHOMA; JESSNERS LYMPHOCYTIC INFILTRATION; PLASMACYTOID DENDRITIC CELLS; BORRELIA-BURGDORFERI; MYCOSIS-FUNGOIDES; ANGIOLYMPHOID HYPERPLASIA; PITYRIASIS LICHENOIDES; LYMPHOPROLIFERATIVE DISORDERS; DIFFERENTIAL-DIAGNOSIS;
D O I
10.1111/cup.13532
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Cutaneous pseudolymphomas (PSLs) belong to a group of lymphocytic infiltrates that histopathologically and/or clinically simulate lymphomas. Different causative agents (e.g., Borrelia sp., injected substances, tattoo, arthropod bite) have been described, but in many cases no cause can be identified, hence the term idiopathic PSL. Clinicopathological correlation is important to make the diagnosis. Four main groups of cutaneous PSL can be distinguished based on histopathologic and/or clinical presentation: (a) nodular PSL; (b) pseudo-mycosis fungoides (pseudo-MF) and simulators of other CTCLs; (c) other PSL (representing distinct clinical entities); and (d) intravascular PSL. This article gives an overview of the histopathologic and clinical characteristics of cutaneous PSLs and proposes a new classification.
引用
收藏
页码:76 / 97
页数:22
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