慢性皮肤移植物抗宿主病中的皮肤病淋巴结病。

Kana Kato, Takeshi Kobayashi, Tsunekazu Hishima, Kaori Kondo, Yasutaka Sadaga, Chika Kato, Satoshi Sakai, Yasuhiro Kambara, Hiroki Fujiwara, Kou Teshima, Kazuya Asano, Yoshimi Nabe, Kazuya Kurihara, Atsushi Jinguji, Masashi Shimabukuro, Fumihiko Ouchi, Kazuki Inai, Naoki Shingai, Takashi Toya, Hiroaki Shimizu, Yuho Najima, Yoshiki Okuyama, Noriko Doki
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引用次数: 0

摘要

一名46岁女性因急性髓系白血病接受脐带血移植7个月后出现慢性皮肤移植物抗宿主病(GVHD)伴双侧腋窝淋巴结(LN)肿胀。组织学检查显示为皮肤病淋巴结病(DL)。局部类固醇治疗后,GVHD改善,淋巴结病消退。DL通常与慢性皮肤病相关,其病理特征是朗格汉斯细胞和间指细胞浸润的皮质旁淋巴结增生。GVHD很少发生LN肿胀,该患者的临床病程提示她的DL是由慢性皮肤GVHD引起的。有趣的是,朗格汉斯细胞的嵌合分析显示了供体来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Dermatopathic lymphadenopathy in chronic skin graft-versus-host disease].

A 46-year-old woman developed chronic skin graft-versus-host disease (GVHD) with bilateral axillary lymph node (LN) swelling 7 months after cord blood transplantation for acute myeloid leukemia. Histological examination of the LNs revealed dermatopathic lymphadenopathy (DL). After treatment with topical steroids, GVHD improved and lymphadenopathy subsided.DL typically occurs associated with chronic dermatologic disorders, and its pathology is characterized by paracortical LN hyperplasia by Langerhans cells and interdigitating cell infiltration. LN swelling rarely occurs with GVHD, and the clinical course in this patient suggests that her DL was caused by chronic skin GVHD. Interestingly, chimerism analysis of the Langerhans cells indicated donor origin.

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