Misbah S A, Spickett G P, Esiri M M, Hughes J T, Matthews W B, Thompson R A, Chapel H M
Department of Immunology, John Radcliffe Hospital, Oxford, UK.
Postgrad Med J. 1992 May;68(799):359-62. doi: 10.1136/pgmj.68.799.359.
A patient with profound panhypogammaglobulinaemia due to common variable immunodeficiency developed two discrete intra-cranial space-occupying lesions, 10 years apart, requiring craniotomy. Histological examination revealed the intra-cranial masses to be granulomata of unknown aetiology on both occasions.
一名因常见变异型免疫缺陷导致严重全低丙种球蛋白血症的患者,在相隔10年的时间里出现了两个独立的颅内占位性病变,需要进行开颅手术。两次组织学检查均显示颅内肿块为病因不明的肉芽肿。