Churkin N L, Mednikov S N
Arkh Patol. 1987;49(4):79-82.
A typical case of Niemann-Pick disease in a 22-month boy is presented. The disease was associated with a CNS lesion, as well as with the impairment of macrophagal-histiocytic system. The study of native material in the polarized light with subsequent confirmation by histochemical methods is considered as a method of choice for diagnosis of lingering diseases beginning in the postnatal period and with a suspicion of thesaurismosis, sphingomyelinosis, in particular.
本文介绍了一名22个月大男童的典型尼曼-匹克病病例。该疾病与中枢神经系统病变以及巨噬细胞-组织细胞系统损伤有关。利用偏振光对天然材料进行研究,并随后通过组织化学方法加以证实,被认为是诊断出生后开始的迁延性疾病,尤其是怀疑有贮积病、鞘磷脂沉积病的首选方法。