Berkman A W, Woog J J, Kickler T S, Ettinger D S
Cancer. 1983 Jun 1;51(11):2057-60. doi: 10.1002/1097-0142(19830601)51:11<2057::aid-cncr2820511117>3.0.co;2-p.
This case report describes a patient who presented with Stage IV B Hodgkin's disease and autoimmune thrombocytopenia. Prior to the institution of therapy the presence of platelet-associated IgG was documented. When the patient was treated with steroids and chemotherapy, the thrombocytopenia resolved and platelet-associated IgG disappeared. Splenectomy alone did not correct the thrombocytopenia. The literature on Hodgkin's disease and autoimmune thrombocytopenia is reviewed.
本病例报告描述了一名患有IV B期霍奇金淋巴瘤和自身免疫性血小板减少症的患者。在开始治疗之前，已记录到血小板相关IgG的存在。当患者接受类固醇和化疗治疗时，血小板减少症得到缓解，血小板相关IgG消失。单纯脾切除术未能纠正血小板减少症。本文对霍奇金淋巴瘤和自身免疫性血小板减少症的文献进行了综述。
