Kan'shina N F, Chemiakin A I, Ozhiganova I N
Arkh Patol. 1986;48(7):78-80.
An observation of the Niemann-Pick disease in a male of 53 is described. The disease developed latently, acute clinical symptoms were provoked by spontaneous rupture of the spleen containing numerous "accumulation" Pick cells. Diagnosis was established after histological examination of the operatively removed spleen.
本文描述了一例53岁男性的尼曼-匹克病。该病呈潜伏性发展,含有大量“蓄积”的匹克细胞的脾脏自发性破裂引发了急性临床症状。经手术切除脾脏的组织学检查后确诊。