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常染色体显性 STAT3 缺乏症患者的鉴别诊断颇具挑战性。

A challenging differential diagnosis in a patient with autosomal dominant STAT3 deficiency.

作者信息

Bravo-Queipo-de-Llano Blanca, Bonet Daniel, Del Rosal Teresa, Cámara Carmen, Ruiz de Valbuena Marta, Pérez Ana, Grasa Carlos D, Méndez-Echevarría Ana

机构信息

Department of Pediatric Infectious and Tropical Diseases, Hospital La Paz, Madrid, Spain.

Center for Biomedical, Hospital La Paz Institute for Health Research (IdiPAZ), La Paz University Hospital, Madrid, Spain.

出版信息

Pediatr Pulmonol. 2023 Feb;58(2):585-591. doi: 10.1002/ppul.26212. Epub 2022 Nov 2.

DOI:10.1002/ppul.26212
PMID:36267002
Abstract

Autosomal dominant hyper IgE syndrome (AD-HIES) is a primary immunodeficiency caused by loss-of-function (LOF) mutations in the Signal Transducer and Activator of Transcription 3 (STAT3) gene. In these patients, performing a correct differential diagnosis of pulmonary infections is difficult and challenging, as they usually have atypical presentations. However, establishing a correct diagnostic and therapeutic approach is essential, as pulmonary complications are responsible for high morbidity and mortality rates in these patients. We report the case of a teenage girl with AD-HIES and respiratory symptoms and fever in whom performing a correct differential diagnosis was challenging.

摘要

常染色体显性高免疫球蛋白E综合征(AD-HIES)是一种由信号转导和转录激活因子3(STAT3)基因功能丧失(LOF)突变引起的原发性免疫缺陷病。在这些患者中,对肺部感染进行正确的鉴别诊断困难且具有挑战性,因为他们通常有非典型表现。然而,建立正确的诊断和治疗方法至关重要,因为肺部并发症是这些患者高发病率和死亡率的原因。我们报告了一例患有AD-HIES的青少年女孩的病例,她有呼吸道症状和发热,对其进行正确的鉴别诊断具有挑战性。

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