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原发性脑淋巴瘤样肉芽肿病在免疫抑制治疗下进展为甲氨蝶呤相关淋巴增殖性疾病。

Primary cerebral lymphomatoid granulomatosis progressing to methotrexate-associated lymphoproliferative disease under immunosuppressive therapy.

作者信息

Tanaka Hiroaki, Furukawa Shogo, Takeda Yusuke, Shimizu Naomi, Kawaguchi Takeharu, Kawajiri Chika, Hashimoto Shinichiro, Takagi Toshiyuki, Ito Shoichi, Ota Satoshi, Kuwabara Satoshi, Nakaseko Chiaki

机构信息

Department of Hematology, Oami Municipal Hospital, Japan.

出版信息

Intern Med. 2015;54(5):503-7. doi: 10.2169/internalmedicine.54.2399. Epub 2015 Jan 15.

Abstract

Lymphomatoid granulomatosis (LYG) is an angiocentric and angiodestructive lymphoproliferative disease involving extranodal sites. Although LYG cerebral lesions are usually located adjacent to LYG pulmonary lesions, few reports have described the occurrence of primary cerebral LYG. We herein discuss a case of a 40-year-old Japanese woman with primary cerebral LYG that caused various neurological symptoms for more than five years and progressed to methotrexate-associated lymphoproliferative disease under treatment with immunosuppressive therapy. This case suggests that primary cerebral LYG should be considered a lymphoid neoplasm manifesting as a primary brain tumor and a component of the differential diagnosis of chronic neuroinflammatory disorders.

摘要

淋巴瘤样肉芽肿病(LYG)是一种累及结外部位的血管中心性和血管破坏性淋巴增殖性疾病。虽然LYG脑病变通常位于LYG肺病变附近,但很少有报告描述原发性脑LYG的发生情况。我们在此讨论一例40岁日本女性原发性脑LYG病例,该病例导致各种神经症状长达五年以上,并在免疫抑制治疗过程中进展为甲氨蝶呤相关淋巴增殖性疾病。该病例提示,原发性脑LYG应被视为一种表现为原发性脑肿瘤的淋巴样肿瘤,也是慢性神经炎症性疾病鉴别诊断的组成部分。

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