Rasso A1*, Chaoui R1, Elloudi S1, Baybay H1, Mernissi FZ1
1Department of dermatology CHU Hassan II, Fez, Morocco
Corresponding Author: Asmae Rasso
Address: Department of Dermatology, CHU Hassan II Fez, Morocco; Tel: 00 212 672314910; E-mail: firstname.lastname@example.org
Received date: 18 February 2020; Accepted date: 02 April 2020; Published date: 19 April 2020
Tuberous sclerosis complex (TSC) is a rare genetic disorder that affects about 1 in 5000 individuals worldwide. It does can affect many organs, leading to benign tumors presenting preferentially in the skin, brain, and kidneys. We report the case of a young man with cutaneous angiofibromes who is incidentally diagnosed with renal angiomyolipoma.
Tuberous sclerosis complex is a rare disease with multi-organic disorders, some of which are severe and often asymptomatic`. The role of the doctor is to make a good clinical and paraclinical examination and a good follow-up of these patients in order to save and improve their quality of life.
Citation: Rasso A, Chaoui R, Elloudi S, Baybay H, Mernissi FZ. When Aesthetic Concern Discovered the Mister: A Renal Angiomyolipoma. Asp Biomed Clin Case Rep. 2020 Apr 8;3(2):99-101.
Copyright © 2020 Rasso A, Chaoui R, Elloudi S, Baybay H, Mernissi FZ. This is an open-access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited.
Keywords: Tuberous Sclerosis Complex; Renal Angiomyolipoma; Abdominal CT scan