淋巴瘤样丘疹病。

Lymphomatoid papulosis.

作者信息

Wiznia Lauren E, Cohen Jeffrey M, Beasley Jenna M, Meehan Shane A, Latkowski Jo-Ann M

机构信息

The Ronald O. Perelman Department of Dermatology, New York University Langone Medical Center, New York, New York.

出版信息

Dermatol Online J. 2018 Dec 15;24(12):13030/qt4xt046c9.

PMID:30677799

Abstract

Lymphomatoid papulosis is often regarded as a low-grade variant of cutaneous T cell lymphoma (CTCL). Given the excellent long-term prognosis, recent consensus guidelines indicate that patients can be monitored off therapy. We report a case of a 67-year-old man who presented with lymphomatoid papulosis, with necrotic papules that have been intermittently present for over forty years.

摘要

淋巴瘤样丘疹病通常被视为皮肤T细胞淋巴瘤（CTCL）的一种低级别变异型。鉴于其良好的长期预后，近期的共识指南指出，患者可以在不接受治疗的情况下进行监测。我们报告一例67岁男性患者，其患有淋巴瘤样丘疹病，伴有坏死性丘疹，这些丘疹间歇性出现已超过40年。