Simultaneous rupture of two renal artery aneurysms in a patient with tuberous sclerosis complex
Autor: | Rafael Santini-Dominguez, Patricia Mulero-Soto, Jorge L. Martinez-Trabal, Sheila Pérez, Alexandra Schoene, Gabriel Pereira |
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Rok vydání: | 2021 |
Předmět: |
congenital
hereditary and neonatal diseases and abnormalities Left renal artery medicine.medical_specialty Angiomyolipoma RD1-811 030204 cardiovascular system & hematology Genetic Condition Retroperitoneal hematoma 030218 nuclear medicine & medical imaging 03 medical and health sciences Tuberous sclerosis Epilepsy 0302 clinical medicine Aneurysm Case report medicine Diseases of the circulatory (Cardiovascular) system Renal artery aneurysms business.industry Renal artery aneurysm Coil embolization medicine.disease Autosomal dominant RC666-701 Surgery Postembolization syndrome Radiology Cardiology and Cardiovascular Medicine business |
Zdroj: | Journal of Vascular Surgery Cases and Innovative Techniques Journal of Vascular Surgery Cases and Innovative Techniques, Vol 7, Iss 2, Pp 364-367 (2021) |
ISSN: | 2468-4287 |
DOI: | 10.1016/j.jvscit.2021.04.004 |
Popis: | Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem neurocutaneous genetic condition. It is characterized by TSC-associated neuropsychiatric disorders, epilepsy, tumors, and angiomyolipoma in multiple organs, such as the skin, lungs, and kidneys. TSC is also associated with the development of aneurysms of the medium and large arteries, including the renal arteries. This condition will usually be diagnosed early in life, and active surveillance is required of tumor and aneurysm growth to prevent life-threatening events. We have presented the case of a 41-year-old patient with TSC that had not been previously diagnosed. The patient had presented with retroperitoneal hematoma secondary to the rupture of two left renal artery branch aneurysms that had likely developed within the angiomyolipoma. |
Databáze: | OpenAIRE |
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