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一名患有复发性脓肿的成年患者的慢性肉芽肿病。

Chronic granulomatous disease in an adult with recurrent abscesses.

作者信息

Perry H B, Boulanger M, Pennoyer D

出版信息

Arch Surg. 1980 Feb;115(2):200-2. doi: 10.1001/archsurg.1980.01380020066015.

Abstract

Chronic granulomatous disease (CGD), produced by an inherited defect in the bactericidal capacity of polymorphonuclear neutrophils, is associated with recurrent abscess formation in regional lymph nodes, pulmonary parenchyma, and liver requiring surgical drainage. It is now becoming increasingly recognized that this is not a uniformly fatal disease of childhood. Instead, patients with milder forms of the disease are being detected during adulthood. General surgeons should be aware of the possibility of this diagnosis in a patient with recurrent pyogenic abscesses requiring drainage. Making the diagnosis of CGD is important because with chronic prophylactic antibiotic therapy and early aggressive treatment of recognized infections, the morbidity and mortality of patients can be favorably influenced. We describe a 27-year-old man with recurrent liver abscesses who was subsequently found to have CGD.

摘要

慢性肉芽肿病(CGD)是由多形核中性粒细胞杀菌能力的遗传性缺陷引起的,与区域淋巴结、肺实质和肝脏反复形成脓肿有关,这些脓肿需要手术引流。现在人们越来越认识到,这并非一种儿童期必然致命的疾病。相反,病情较轻的患者在成年期被发现。普通外科医生应意识到,对于需要引流反复化脓性脓肿的患者,有这种诊断的可能性。诊断CGD很重要,因为通过慢性预防性抗生素治疗和对已确认感染的早期积极治疗,可以对患者的发病率和死亡率产生有利影响。我们描述了一名27岁反复发生肝脓肿的男性,他随后被发现患有CGD。

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