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I/IIA期蕈样肉芽肿患者新肿瘤的评估

Evaluation of new tumors in the setting of stage I/IIA mycosis fungoides.

作者信息

Harrington Cynthia R, Guillén David R, Pandya Amit G

机构信息

Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9190, USA.

出版信息

Clin Lymphoma Myeloma. 2007 Jul;7(7):480-5. doi: 10.3816/clm.2007.n.032.

Abstract

Although mycosis fungoides is usually a slowly progressive indolent lymphoma, new cutaneous tumors might signal an aggressive phase of the disease. In order to provide appropriate therapeutic management when such tumors arise, it is important to make a correct diagnosis, which requires a bridge between clinical and histopathologic evaluations of the tumors. In this article, we describe 4 patients with preexisting diagnoses of mycosis fungoides, each of whom developed a distinct, new skin tumor. These tumors represented the following: mycosis fungoides without transformation, large-cell transformation of mycosis fungoides, lymphomatoid papulosis-associated CD30(+) lymphoproliferative disorder arising in a patient with mycosis fungoides, and a primary cutaneous CD30(+) lymphoproliferative disorder arising in a patient with mycosis fungoides. Each new and histologically distinct tumor was identified and treated according to a diagnosis concluded by careful clinicopathologic correlation, allowing for the selection of appropriate treatment in each case.

摘要

虽然蕈样肉芽肿通常是一种进展缓慢的惰性淋巴瘤,但新出现的皮肤肿瘤可能预示着疾病进入侵袭性阶段。为了在这类肿瘤出现时提供恰当的治疗管理,做出正确诊断很重要,这需要在肿瘤的临床评估和组织病理学评估之间架起一座桥梁。在本文中,我们描述了4例先前已诊断为蕈样肉芽肿的患者,他们每人都出现了一种独特的新发皮肤肿瘤。这些肿瘤分别为:未发生转化的蕈样肉芽肿、蕈样肉芽肿的大细胞转化、蕈样肉芽肿患者中出现的与淋巴瘤样丘疹病相关的CD30(+)淋巴增殖性疾病,以及蕈样肉芽肿患者中出现的原发性皮肤CD30(+)淋巴增殖性疾病。通过仔细的临床病理相关性分析得出诊断结论,识别并治疗了每一种新的、组织学上不同的肿瘤,从而为每种情况选择了合适的治疗方法。

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