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中枢神经系统受累于恶性萎缩性丘疹病(科尔迈尔-德戈斯病):血管病和凝血病。

CNS involvement in malignant atrophic papulosis (Kohlmeier-Degos disease): vasculopathy and coagulopathy.

作者信息

Dastur D K, Singhal B S, Shroff H J

出版信息

J Neurol Neurosurg Psychiatry. 1981 Feb;44(2):156-60. doi: 10.1136/jnnp.44.2.156.

Abstract

The clinical features in a 42 year old man with malignant atrophic papulosis with CNS involvement are described. They included mental dysfunction, paraesthesiae, weakness of left limbs, with pyramidal tract signs, bilateral ptosis, progressing to total ophthalmoplegia and obtundation. There were two crops of characteristic papular lesions on trunk and limbs, with terminal evidence of a coagulopathy and bruises, resulting in death in six months. Papular biopsy revealed multiple microinfarcts in the dermal collagen. The brain showed multiple small haemorrhagic infarcts of both hemispheres, the lower mid-brain, pons and a cerebellar peduncle. Microscopy showed fibrin exudation in the leptomeninges, various stages of thrombosis of small arteries without inflammatory reaction, and corresponding acute and subacute microinfarcts. The pathogenetic basis of the disease appeared to be a combined vasculopathy and coagulopathy.

摘要

描述了一名42岁患有中枢神经系统受累的恶性萎缩性丘疹病男性的临床特征。这些特征包括精神功能障碍、感觉异常、左下肢无力并伴有锥体束征、双侧上睑下垂,进而发展为完全性眼肌麻痹和昏迷。躯干和四肢有两批特征性丘疹病变,最终出现凝血障碍和瘀斑的证据,患者在6个月后死亡。丘疹活检显示真皮胶原中有多个微梗死灶。脑部显示双侧半球、中脑下部、脑桥和一个小脑脚有多个小出血性梗死灶。显微镜检查显示软脑膜有纤维蛋白渗出,小动脉有不同阶段的血栓形成且无炎症反应,以及相应的急性和亚急性微梗死灶。该疾病的发病机制基础似乎是血管病变和凝血障碍的联合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d34/490849/e1b26492491e/jnnpsyc00058-0069-a.jpg

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