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色素失禁症的神经病理学研究。解剖学病例报告(作者译)

[Neuropathological study of incontinentia pigmenti. Anatomical case report (author's transl)].

作者信息

Hauw J J, Perié G, Bonnette J, Escourolle R

出版信息

Acta Neuropathol. 1977 May 16;38(2):159-62. doi: 10.1007/BF00688564.

Abstract

Report of a case of Incontinentia pigmenti (IP) of the Bloch-Sulzberger type, with neurological features, in a 3 month-old deceased infant. The neuropathological examination revealed signs of a destructive process which had occurred in the perinatal period: ulegyria, cavities of white matter and patchy scar softening of the cerebellar cortex. In addition, there was a diffuse inflammatory process involving the pia-arachnoid and brain tissue: perivascular cuffs of lymphocytes, histiocytes and eosinophilic polymorphs, and mononuclear nodules. No prenatal malformations or vascular lesions were found. These findings are discussed in the light of both the relevant literature on neurological abnormalities in IP and the only already reported neuropathological examination by O'Doherty and Norman (1968). Two main hypotheses might account for the frequency of neurological disturbances in IP, 1. a peculiar sensitivity of the brain to anoxia and/or ischemia: 2. its involvement by the specific inflammatory process which occurs both in the skin as other tissues in this genetically determined disease (Perié et al., 1976).

摘要

一名3个月大已死亡婴儿的布洛赫-苏尔茨贝格型色素失禁症(IP)病例报告,该病例具有神经学特征。神经病理学检查显示在围产期发生了破坏性病变的迹象:脑回状瘢痕、白质空洞以及小脑皮质的斑片状瘢痕软化。此外,存在累及软脑膜和脑组织的弥漫性炎症过程:淋巴细胞、组织细胞和嗜酸性多形核细胞的血管周围套袖,以及单核结节。未发现产前畸形或血管病变。结合IP神经异常的相关文献以及奥多尔蒂和诺曼(1968年)唯一已报道的神经病理学检查对这些发现进行了讨论。关于IP中神经功能障碍的发生率,可能有两个主要假说:1. 大脑对缺氧和/或缺血具有特殊敏感性;2. 在这种遗传决定的疾病中,皮肤和其他组织中发生的特定炎症过程累及大脑(佩里等人,1976年)。

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