Christopoulos C, Papadaki T, Vlavianos P, Kokkini G
Clinical Haematology Unit, Sismanoglio General Hospital, Athens, Greece.
J Clin Pathol. 1995 Sep;48(9):871-3. doi: 10.1136/jcp.48.9.871.
A 61 year old man with long standing common variable immunodeficiency presented with pyrexia, anaemia and leucopenia. A diagnoses of Hodgkin's disease of the bone marrow was made. The typical histopathological and immunophenotypic appearances were clearly distinct from those of T cell lymphoma with Reed-Sternberg-like cells which, in contrast to Hodgkin's disease, is a known complication of common variable immunodeficiency. Complete clinical and histological remission was achieved with combination chemotherapy. The latter was complicated by severe myelosuppression, unusually severe erosive mucositis and viral retinitis.
一名患有长期常见可变免疫缺陷的61岁男性出现发热、贫血和白细胞减少。诊断为骨髓霍奇金病。典型的组织病理学和免疫表型表现与伴有里德-施特恩伯格样细胞的T细胞淋巴瘤明显不同,与霍奇金病相反,后者是常见可变免疫缺陷的已知并发症。联合化疗实现了完全的临床和组织学缓解。后者伴有严重的骨髓抑制、异常严重的糜烂性粘膜炎和病毒性视网膜炎。