Beck J D, Weinig J E, Müller-Hermelink H K, Lemmel E M
Eur J Pediatr. 1977 Oct 12;126(3):175-84. doi: 10.1007/BF00442199.
The case history of a 9 months old infant with hepatosplenomegaly, pancytopnaenia and disturbances of clotting and cellular immune reactivity is reported. The spleen was removed and showed striking erythrophagocytosis by proliferating histiocytes, typical of "familial erythrophagocytic reticulosis" (Farquhar). A graft-versus-host reaction is discussed as a possible underlying cause. The favourable clinical course and full recovery point to an interrelation with primary hypersplenism.
报告了一名9个月大婴儿的病史,该婴儿患有肝脾肿大、全血细胞减少以及凝血和细胞免疫反应紊乱。切除的脾脏显示增生的组织细胞有显著的红细胞吞噬现象,这是“家族性噬血细胞性网状细胞增多症”(法夸尔)的典型表现。讨论了移植物抗宿主反应作为可能的潜在病因。良好的临床病程和完全康复表明与原发性脾功能亢进有关。