1. A Case With Wiskott-Aldrich Syndrome and Ascending Aorta Aneurysm
- Author
-
Adnan Barutçu, Fadli Demir, Serife Leblebisatan, Metin Cil, Göksel Leblebisatan, and Hatice Şaşmaz
- Subjects
Male ,medicine.medical_specialty ,Wiskott–Aldrich syndrome ,macromolecular substances ,Disease ,Aneurysm ,medicine.artery ,Ascending aorta ,medicine ,Humans ,Ascending aorta aneurysm ,Child ,Aorta ,Immunodeficiency ,medicine.diagnostic_test ,business.industry ,Magnetic resonance imaging ,Hematology ,medicine.disease ,Thrombocytopenia ,Aortic Aneurysm ,Wiskott-Aldrich Syndrome ,Surgery ,Oncology ,Pediatrics, Perinatology and Child Health ,cardiovascular system ,Primary immunodeficiency ,business - Abstract
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.
- Published
- 2020