Nakagiri Tomoyuki, Okumura Meinoshin, Inoue Masayoshi, Minami Masato, Kiyohara Eiji, Umegaki Noriko, Nakamura Toshiaki, Tomita Yasuhiko, Katayama Ichirou, Aozasa Katsuyuki
Department of General Thoracic Surgery, Osaka University Graduate School of Medicine, Suita City, Osaka, Japan.
J Thorac Oncol. 2007 Dec;2(12):1130-2. doi: 10.1097/JTO.0b013e31815ba23a.
We report a 40-year-old woman with recurrent thymoma associated with myasthenia gravis, in whom an unusual form of erythroderma developed. A histological examination revealed a graft-versus-host disease (GVHD)-like reaction. After high-dose steroid therapy, the metastatic thymoma lesion in the abdominal cavity was reduced in size from 9.5 x 6 x 7.5 cm to 4 x 3 x 1 cm in diameter. Nevertheless, the GVHD-like erythroderma become aggravated, her condition worsened, and the patient finally suffered from respiratory failure and died of sepsis. A GVHD-like reaction may be a rare presentation of thymoma-associated immunological disorders such as myasthenia gravis or pure red cell aplasia. Herein, we discuss the present case and review pertinent reports of thymoma cases associated with GVHD.
我们报告了一名40岁患有复发性胸腺瘤并伴有重症肌无力的女性患者,该患者出现了一种不寻常的红皮病形式。组织学检查显示为移植物抗宿主病(GVHD)样反应。大剂量类固醇治疗后,腹腔内转移性胸腺瘤病变直径从9.5×6×7.5厘米缩小至4×3×1厘米。然而,GVHD样红皮病却加重了,她的病情恶化,患者最终因呼吸衰竭死于败血症。GVHD样反应可能是胸腺瘤相关免疫紊乱(如重症肌无力或纯红细胞再生障碍)的一种罕见表现。在此,我们讨论该病例并回顾与GVHD相关的胸腺瘤病例的相关报告。