Splenic Artery Aneurysms, a Rare Complication of Type 1 Gaucher Disease: Report of Five Cases
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Titre | Splenic Artery Aneurysms, a Rare Complication of Type 1 Gaucher Disease: Report of Five Cases |
Type de publication | Journal Article |
Year of Publication | 2019 |
Auteurs | Serratrice C, Cox TM, Leguy-Seguin V, Morris E, Yousfi K, Monnet O, Sibert A, Allaham W, Belmatoug N |
Journal | JOURNAL OF CLINICAL MEDICINE |
Volume | 8 |
Pagination | 219 |
Date Published | FEB |
Type of Article | Article |
ISSN | 2077-0383 |
Mots-clés | enzyme replacement therapy, Gaucher disease, lysosomal storage disorder, splenic arterial aneuryms |
Résumé | Type 1 Gaucher disease is a rare genetic lysosomal disorder due to acid betaglucosidase deficiency. The main features are thrombocytopenia, anemia, hepatosplenomegaly and complex skeletal disease. Complications include pulmonary hypertension, cirrhosis and splenic infarction; comorbidities, such as autoimmune phenomena, B-cell malignancies and Parkinson disease also occur. Visceral aneurysms have been only rarely noted in Gaucher disease. We report the retrospective data from patients with Gaucher disease type 1 and splenic arterial aneurysm. We describe the different outcomes of a giant splenic arterial aneurysm in five patients with type 1 Gaucher disease and discuss the main possible pathophysiological explanations. Aneurysms of the splenic artery are rare in Gaucher disease but are probably greatly under-reported. |
DOI | 10.3390/jcm8020219 |