Suppr超能文献

[鼻红粒病与嗜铬细胞瘤]

[Granulosis rubra nasi and pheochromocytoma].

作者信息

Heid E, Samain F, Jelen G, Boivin S

机构信息

Clinique Dermatologique, Hôpitaux Universitaires, Strasbourg.

出版信息

Ann Dermatol Venereol. 1996;123(2):106-8.

PMID:8761763
Abstract

INTRODUCTION

Granulosis rubra nasi, a papular red lesion of the nose associated with hypersudation is an uncommon dermatosis usually seen in children.

CASE REPORT

A noradrenalin secreting pheochromocytoma was found in 19-year-old girl with hyperhidrosis, granulosis rubra nasi and tachycardia. Surgical exeresis of the pheochromocytoma was followed by involution of the hyperhidrosis, regression of the nasal dermatosis and normalization of urinary catecholamines.

DISCUSSION

The diagnosis of pheochromocytoma should be entertained in patients with hypersudation and tachycardia. Granulosis rubra nasi could be a complication of hyperhidrosis.

摘要

引言

鼻红粒病是一种与多汗症相关的鼻部丘疹性红色病变,是一种罕见的皮肤病,多见于儿童。

病例报告

在一名患有多汗症、鼻红粒病和心动过速的19岁女孩中发现了一个分泌去甲肾上腺素的嗜铬细胞瘤。嗜铬细胞瘤手术切除后,多汗症消退,鼻部皮肤病好转,尿儿茶酚胺恢复正常。

讨论

对于多汗症和心动过速患者应考虑嗜铬细胞瘤的诊断。鼻红粒病可能是多汗症的一种并发症。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验