

Publisher: John Wiley & Sons Inc
E-ISSN: 1525-1470|32|3|423-424
ISSN: 0736-8046
Source: PEDIATRIC DERMATOLOGY, Vol.32, Iss.3, 2015-05, pp. : 423-424
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
AbstractAngiomyolipomas are benign tumors composed of blood vessels, smooth muscle, and adipose tissue that are frequently associated with tuberous sclerosis. Cutaneous angiomyolipomas are rare and typically present in men in the fifth or sixth decade of life. We present a case of a cutaneous angiomyolipoma masquerading as a neurofibroma in a 13‐year‐old boy with a history of neurofibromatosis type 1.
Related content


Intrahepatic plexiform neurofibroma with neurofibromatosis type 1
PEDIATRICS INTERNATIONAL, Vol. 60, Iss. 1, 2018-01 ,pp. :


An extreme case of neurofibromatosis type 1
By Štimac Davor Novak Srdjan Guina Tina
Wiener klinische Wochenschrift, Vol. 119, Iss. 3-4, 2007-03 ,pp. :




Nevus Anemicus: A Distinctive Cutaneous Finding in Neurofibromatosis Type 1
PEDIATRIC DERMATOLOGY, Vol. 32, Iss. 3, 2015-05 ,pp. :