A Case of an Splenic Artery Aneurysm and Focal Nodular Hyperplasia Associated with an Abdominal Vascular Abnormality of Hereditary Hemorrhagic Telangiectasia
Author:
Affiliation:
1. Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan
2. Department of Dermatology, Saiseikai Tondabayashi Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/advpub/0/advpub_3270-23/_pdf
Reference19 articles.
1. 1. Osler W. On a family form of recurring epistaxis, associated with multiple telangiectasias of the skin and mucous membranes. Johns Hopkins Hos Bull 128: 333-337, 1901.
2. 2. Hanes F. Multiple hereditary telangiectases causing hemorrhage (hereditary hemorrhage telangiectasia). Bull John Hopkins Hosp 20: 63-73, 1909.
3. 3. Begbie ME, Wallace GMF, Shovlin CL. Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): A view from the 21st century. Postgrad Med J 79: 18-24, 2003.
4. 4. Shovlin CL, Guttmacher AE, Buscarini E, et al. Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 91: 66-67, 2000.
5. 5. Shovlin CL, Hughes JMB, Tuddenham EGD, et al. A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3. Nat Genet 6: 205-209, 1994.
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