ANGIOFIBROMA: A RARE CASE

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EHSANI AMIR HOUSHANG; NOURMOHAMMADPOUR P.; MORADI ATA ELAH

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Journal: Dermatology and Cosmetics Year:2010 | Volume:1 | Issue:1 Page(s): 44-46

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Title

ANGIOFIBROMA: A RARE CASE

Author(s)

EHSANI AMIR HOUSHANG | NOURMOHAMMADPOUR P. | MORADI ATA ELAH | Issue Writer Certificate

Keywords

ANGIOFIBROMAQ3

FACEQ3

TUBEROUS SCLEROSIS COMPLEXQ3

Abstract

Tuberous sclerosis complex is a genetic disorder characterized by hamartoma formation in many organs. Its characteristic dermatologic manifestations include ANGIOFIBROMA, shagreen patch, periungual fibroma and white macules. This disorder is usually accompanied by epilepsy and mental deficiency. Here, a 26-year-old man is presented who has been referred to a teaching hospital with a huge facial ANGIOFIBROMA which had led to major psychological problems for him necessitating and appropriate treatment plan.

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APA: Copy

EHSANI, AMIR HOUSHANG, NOURMOHAMMADPOUR, P., & MORADI, ATA ELAH. (2010). ANGIOFIBROMA: A RARE CASE. DERMATOLOGY AND COSMETIC, 1(1), 44-46. SID. https://sid.ir/paper/157693/en

Vancouver: Copy

EHSANI AMIR HOUSHANG, NOURMOHAMMADPOUR P., MORADI ATA ELAH. ANGIOFIBROMA: A RARE CASE. DERMATOLOGY AND COSMETIC[Internet]. 2010;1(1):44-46. Available from: https://sid.ir/paper/157693/en

IEEE: Copy

AMIR HOUSHANG EHSANI, P. NOURMOHAMMADPOUR, and ATA ELAH MORADI, “ANGIOFIBROMA: A RARE CASE,” DERMATOLOGY AND COSMETIC, vol. 1, no. 1, pp. 44–46, 2010, [Online]. Available: https://sid.ir/paper/157693/en

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