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一名重症肌无力患者出现了自身免疫性血小板减少性紫癜、自身免疫性溶血性贫血和胃癌。

Autoimmune thrombocytopenic purpura, autoimmune hemolytic anemia and gastric cancer appeared in a patient with myasthenia gravis.

作者信息

Wakata Nobuo, Kiyozuka Tetsuhito, Konno Singo, Nakazora Hiroshi, Nomoto Nobuatsu, Sugimoto Hideki, Nemoto Hiroshi

机构信息

Department of Neurology, Toho University School of Medicine, Oohashi Hospital, Tokyo.

出版信息

Intern Med. 2006;45(7):479-81. doi: 10.2169/internalmedicine.45.1496. Epub 2006 May 1.

Abstract

We report a case of myasthenia gravis (MG) associated with autoimmune thrombocytopenic purpura (AITP) and autoimmune hemolytic anemia (AIHA), and after that gastric cancer appeared. A 51-year-old man began to suffer from fluctuated muscle weakness in 1985. Muscle weaknesses became exacerbated, and he was admitted to our hospital in 1989. He was diagnosed as MG associated with AITP. After a thymectomy (hyperplasia), prednisolone therapy was started, subsequently his condition was satisfactory. In March 1995, he developed severe anemia and icterus. He was diagnosed as Evans' syndrome (AIHA and AITP) with MG. High-doses of immunoglobulin administration improved the anemia, but thrombocytopenia continued. In November 2002, he suffered marked petechia; the platelet count decreased to 1000/microl. Methylprednisolone pulse therapy and platelet transfusion were started. Gastrofiberscopy was performed and biopsy specimens revealed signet cell-type adenocarcinoma. On December 19, 2002, subtotal gastrectomy and splenectomy were performed. After that, his condition has remained satisfactory, without MG symptoms or thrombocytopenia. This is the first such case report in the literature.

摘要

我们报告一例重症肌无力(MG)合并自身免疫性血小板减少性紫癜(AITP)和自身免疫性溶血性贫血(AIHA),之后又出现胃癌的病例。一名51岁男性于1985年开始出现波动性肌无力。肌无力加重,于1989年入院。他被诊断为合并AITP的MG。胸腺切除(增生)术后,开始使用泼尼松龙治疗,随后病情好转。1995年3月,他出现严重贫血和黄疸。他被诊断为合并MG的伊文氏综合征(AIHA和AITP)。大剂量免疫球蛋白治疗改善了贫血,但血小板减少仍持续存在。2002年11月,他出现明显的瘀点;血小板计数降至1000/微升。开始进行甲泼尼龙冲击治疗和血小板输注。进行了胃镜检查,活检标本显示为印戒细胞型腺癌。2002年12月19日,进行了胃大部切除术和脾切除术。此后,他的病情一直良好,无MG症状或血小板减少。这是文献中首例此类病例报告。

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