Björkholm M, Holm G, Merk K
Cancer. 1982 Apr 15;49(8):1702-4. doi: 10.1002/1097-0142(19820415)49:8<1702::aid-cncr2820490827>3.0.co;2-i.
The case report of a 52-year-old woman with an eight-year history of cyclic autoimmune hemolytic anemia and progressive splenic enlargement is presented. At laparotomy the enlarged spleen and splenic hilar lymph nodes showed lymphocyte-predominant Hodgkin's disease. No specific antitumor treatment was given and three years following splenectomy the patient is in excellent health and has not experienced any new hemolytic episodes. The patient illustrates the association between Hodgkin's disease and autoimmune hemolytic anemia as well as the extreme variation in the clinical picture of the disease.
本文报告了一名52岁女性患者，她有八年周期性自身免疫性溶血性贫血病史且脾脏进行性肿大。剖腹手术时发现，肿大的脾脏和脾门淋巴结显示为淋巴细胞为主型霍奇金病。未给予特殊抗肿瘤治疗，脾切除术后三年，患者健康状况良好，未出现任何新的溶血发作。该患者说明了霍奇金病与自身免疫性溶血性贫血之间的关联以及该疾病临床表现的极端变异性。
