Barnett J L, McDonnell W M, Appelman H D, Dobbins W O
Department of Internal Medicine, University of Michigan Hospital, Ann Arbor.
Gastroenterology. 1992 Feb;102(2):684-91. doi: 10.1016/0016-5085(92)90121-e.
A family with a visceral neuropathy manifested as chronic idiopathic intestinal pseudo-obstruction is reported. Diagnoses were made histologically by simple rectal biopsy. Discrete eosinophilic intranuclear inclusions, diagnostic of a disease known as neuronal intranuclear inclusion disease, were found in the submucosal ganglion cells. Abnormalities of the autonomic nervous system were identified by pupillary examination and electroretinography. In this family, three of four siblings were affected by the disease, which is apparently transmitted from the paternal side. This pedigree was unique for several reasons: (a) diagnosis in multiple members of two generations indicates that this familial visceral neuropathy was expressed in an autosomal dominant manner, (b) central autonomic nervous system abnormalities were detected by eye examination, and (c) the definitive pathological diagnosis was established antemortem by rectal biopsy in all cases.
本文报告了一个患有以慢性特发性肠道假性梗阻为表现的内脏神经病的家族。通过简单的直肠活检进行组织学诊断。在黏膜下神经节细胞中发现了离散的嗜酸性核内包涵体,这是一种名为神经元核内包涵体病的疾病的诊断依据。通过瞳孔检查和视网膜电图确定自主神经系统异常。在这个家族中,四个兄弟姐妹中有三个受该病影响,该病显然是从父系遗传而来。这个家系有几个独特之处:(a) 两代人中多个成员的诊断表明这种家族性内脏神经病以常染色体显性方式表现,(b) 通过眼部检查发现中枢自主神经系统异常,以及 (c) 在所有病例中均通过直肠活检在生前确立了明确的病理诊断。