A Case With Wiskott-Aldrich Syndrome and Ascending Aorta Aneurysm

被引：1

作者：

Barutcu, Adnan ^{[1
]}

Leblebisatan, Goksel ^{[2
]}

Leblebisatan, Serife ^{[4
]}

Cil, Metin ^{[2
]}

Sasmaz, Hatice I. ^{[2
]}

Demir, Fadli ^{[3
]}

机构：

[1] Halfeti State Hosp, Dept Pediat, TR-63950 Sanliurfa, Turkey

[2] Cukurova Univ, Med Fac, Dept Pediat Hematol, Adana, Turkey

[3] Cukurova Univ, Med Fac, Dept Pediat Cardiol, Adana, Turkey

[4] Adana City Training & Res Hosp, Dept Radiol, Adana, Turkey

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2021年 / 43卷 / 06期

关键词：

aortic dilatation; immune thrombocytopenic purpura; resistant thrombocytopenia; Wiskott-Aldrich syndrome; RESECTION;

D O I：

10.1097/MPH.0000000000001932

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency disorder that is characterized by a triad of microthrombocytopenia, severe immunodeficiency, and eczema. We report the case of a 7-year-old male patient with chronic thrombocytopenia that was diagnosed as WAS after dilatation of the ascending aorta was noticed. WAS is rare, and it is a disease that requires high suspicion for diagnosis. We recommend periodic echocardiography and magnetic resonance imaging examinations to evaluate aortic aneurysms in children with WAS and that surgical intervention should not be delayed when aneurysm is detected.

引用

页码：E774 / E776

页数：3

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