Niggli F, Halle F, Seger R A
Universitäts-Kinderklinik, Zürich.
Monatsschr Kinderheilkd. 1991 Nov;139(11):772-4.
This study concerns 3 cases of visceral leishmaniasis with various immunological complications. One patients showed a life-threatening activation of macrophages, characterised by haemophagocytosis in the bone marrow, pancytopenia, hypofibrinogenaemia and hypertriglycerideamia. A selective deficiency of IgG subclasses persisting for months was found in all 3 cases, the clinical relevance of which is unclear. One case manifested the already well known transient decrease of cell mediated immunity to antigens. If early detection and correct management is possible, these complications may be prevented and most cases of visceral leishmaniasis be cured.
本研究涉及3例伴有各种免疫并发症的内脏利什曼病。1例患者出现危及生命的巨噬细胞活化,其特征为骨髓中的噬血细胞现象、全血细胞减少、纤维蛋白原血症和高甘油三酯血症。在所有3例患者中均发现IgG亚类选择性缺乏持续数月,其临床相关性尚不清楚。1例患者表现出对抗原的细胞介导免疫的短暂下降,这一情况已为人熟知。如果能够早期发现并进行正确处理,这些并发症可能得以预防,大多数内脏利什曼病病例也可治愈。