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Thymoma with idiopathic thrombocytopenic purpura preceded by mediastinal hemorrhage; report of a case

机译:胸腺瘤伴特发性血小板减少性紫癜伴纵隔出血;案件报告

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A 62-year-old female with chest and right shoulder pain admitted to a hospital. The chest computed tomography (CT) scan showed a large anterior mediastinum mass with pleural effusion. Thymoma was suspected by percutaneous aspiration biopsy of it. She was referred to our hospital for operation with decreased serum platelet count (7.0 x 10(4)/microliter) and high platelet associated IgG (PA IgG) level (119.5 ng/10(7) cells). Result of bone marrow examination was normal, splenomegaly was not seen and no other autoimmune disease was not detected, so she was thought to have ITP. After giving her intravenous high-dose gamma-globulin and her platelet count increased to normal, operation was done. Extended thymectomy was performed and postoperative course was uneventful. Pathological finding showed the mass mediastinum hematoma in thymus and there found a small thymoma. The hemorrhage was thought to occur from the thymoma. After the operation, her platelet count has not been changed to normal but remained lower level. Though myasthenia gravis, one of the autoimmune disease, improve after total thymectomy, it is thought that idiopathic thrombocytopenic purpura (ITP) could not improve after thymectomy.
机译:一名62岁的女性因胸部和右肩疼痛入院。胸部计算机断层扫描(CT)扫描显示前纵隔肿大并伴有胸腔积液。经胸腔穿刺活检怀疑胸腺瘤。她因血清血小板计数降低(7.0 x 10(4)/微升)和高血小板相关IgG(PA IgG)水平(119.5 ng / 10(7)细胞)而被转诊至我院进行手术。骨髓检查结果正常,未见脾肿大,未检测到其他自身免疫性疾病,因此被认为患有ITP。给她静脉注射大剂量的γ-球蛋白后,她的血小板计数增加到正常水平,进行了手术。进行了胸腺切除术,术后病情进展顺利。病理检查发现胸腺有纵隔血肿,并有小胸腺瘤。认为出血是由于胸腺瘤引起的。手术后,血小板计数未恢复正常但仍保持较低水平。虽然全胸腺切除术后重症肌无力是一种自身免疫性疾病,但可以缓解,但人们认为胸腺切除术后特发性血小板减少性紫癜(ITP)不能改善。

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