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原发性皮肤霍奇金淋巴瘤:一种极其罕见的疾病。

Primary Cutaneous Hodgkin's Lymphoma: An Extremely Rare Entity.

作者信息

Hakkou Darine, Belefqih Ismail, Sabri Samia, Dikhaye Siham, Bachir Houda, Hamaz Siham, Alaoui Habiba, Serraj Khalid

机构信息

Internal Medicine, Mohammed First University, Oujda, MAR.

Internal Medicine, Mohammed VI University Hospital, Mohammed First University, Oujda, MAR.

出版信息

Cureus. 2021 Nov 5;13(11):e19272. doi: 10.7759/cureus.19272. eCollection 2021 Nov.

Abstract

Skin involvement in Hodgkin's lymphoma (HL) is rare. The diagnosis can be difficult, mainly due to the wide range of cutaneous lesions that can be observed, but also due to the differential diagnosis, even after the immunohistochemical staining. We present the case of a 30-year-old man who presented with a painful cutaneous nodular lesion; biopsy and immunohistochemical stains were consistent with classic HL. The patient was treated with adriamycin, bleomycin, vinblastin, and dacarbazine (ABVD) with complete remission.

摘要

皮肤受累于霍奇金淋巴瘤(HL)较为罕见。诊断可能会很困难,这主要是因为可观察到的皮肤病变范围广泛,而且即使在进行免疫组化染色后,鉴别诊断也存在困难。我们报告了一例30岁男性患者,其出现了一个疼痛性皮肤结节性病变;活检及免疫组化染色结果与经典型HL相符。该患者接受了阿霉素、博来霉素、长春花碱和达卡巴嗪(ABVD)治疗,实现了完全缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0728/8643714/300611c2cef6/cureus-0013-00000019272-i01.jpg

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