Pai syndrome: a report of a case and review of the literature

被引：22

作者：

Al-Mazrou, KA

Al-Rekabi, A

Alorainy, IA

Al-Kharfi, T

Al-Serhani, AM

机构：

[1] King Abdulaziz Univ Hosp, Dept Otolaryngol, Riyadh 11411, Saudi Arabia

[2] King Saud Univ, Coll Med, King Khalid Univ Hosp, Dept Histopathol, Riyadh 11461, Saudi Arabia

[3] King Saud Univ, Coll Med, King Khalid Univ Hosp, Dept Radiol, Riyadh 11461, Saudi Arabia

[4] King Saud Univ, Coll Med, King Khalid Univ Hosp, Dept Pediat, Riyadh 11461, Saudi Arabia

来源：

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY | 2001年 / 61卷 / 02期

关键词：

Pai syndrome; upper lip cleft; cutaneous polyps; intracranial lipoma;

D O I：

10.1016/S0165-5876(01)00555-9

中图分类号：

R76 [耳鼻咽喉科学];

学科分类号：

100213 ;

摘要：

Pai syndrome is a rare congenital disorder first described in 1987. The main clinical features of the syndrome include median cleft of the upper lip, intra-cranial lipoma, and cutaneous polyps. Only four cases have been described previously. This is the fifth who is a twin of Arabian descent to be reported. Full description of the clinico-pathological features and a review of the relevant medical literature is presented. To the best of our knowledge, this is the first case of Pai syndrome in a twin in the English literature. (C) 2001 Published by Elsevier Science Ireland Ltd.

引用

页码：149 / 153

页数：5

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