Møller T, Hasselbalch H C
Epidemiafdeling M, Rigshospitalet, København.
Ugeskr Laeger. 1993 May 10;155(19):1442-6.
Infection with human immunodeficiency virus type 1 (HIV-1) primarily involves a subgroup of T-lymphocytic cells, but other cell types are also invaded by the virus, including cell lines within the haematopoietic system. Together with infectious, inflammatory and neoplasic processes, invasion of haematopoietic tissue explains the haematological alterations which are seen during the course of infection with HIV-1. Anaemia develops in the large proportion of patients. Thrombocytopenia frequently occurs during the course of the disease, but may be seen in some patients already at the time of diagnosis, where the condition may be misdiagnosed as "idiopathic" thrombocytopenic purpura. Neutropenia is seen in all disease stages, but is most severe in patients with advanced disease. Bone marrow changes include varying degrees of dysplasia in one or more cell lines, which in some patients may mimic a myelodysplastic syndrome. The number of plasma cells is always increased. In many patients the bone marrow stroma exhibits an increased amount of reticular fibres. HIV-1 infection is associated with an increased risk of non-Hodgkin malignant lymphoma. Acute myelogenous leukaemia and myelomatosis have been described in patients with advanced disease. Treatment of the above mentioned haematological abnormalities aims primarily at reducing replication of HIV-1, thereby diminishing suppression of haematopoiesis by the virus infection, and at controlling the opportunistic infections during the course of the disease. Specific antiviral therapy (AZT) is most successful in correcting thrombocytopenia. The possibility of bone marrow suppression mediated by a toxic drug effect should always be considered in this patient group.
1型人类免疫缺陷病毒(HIV-1)感染主要累及T淋巴细胞亚群,但该病毒也会侵袭其他细胞类型,包括造血系统内的细胞系。连同感染性、炎症性和肿瘤性过程一起,造血组织的侵袭解释了HIV-1感染过程中出现的血液学改变。大部分患者会出现贫血。血小板减少症在疾病过程中经常发生,但在一些患者诊断时就可能出现,此时该病症可能被误诊为“特发性”血小板减少性紫癜。中性粒细胞减少症在所有疾病阶段均可见,但在疾病晚期患者中最为严重。骨髓改变包括一个或多个细胞系不同程度的发育异常,在一些患者中可能类似骨髓增生异常综合征。浆细胞数量总是增加。许多患者的骨髓基质网状纤维数量增多。HIV-1感染与非霍奇金恶性淋巴瘤风险增加相关。晚期疾病患者中已描述有急性髓性白血病和骨髓瘤。上述血液学异常的治疗主要旨在减少HIV-1复制,从而减轻病毒感染对造血的抑制,并控制疾病过程中的机会性感染。特异性抗病毒治疗(齐多夫定)在纠正血小板减少症方面最为成功。对于该患者群体,应始终考虑有毒药物效应介导的骨髓抑制可能性。