These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Eccrine angiomatous hamartoma: a case report and review of the literature. Author: Martinelli PT, Tschen JA. Journal: Cutis; 2003 Jun; 71(6):449-55. PubMed ID: 12839255. Abstract: Eccrine angiomatous hamartoma (EAH) is a rare, benign condition recognized histologically by increased numbers of eccrine elements, as well as numerous vascular channels. Patients typically present with a solitary, sometimes enlarging, nodule of the extremities usually appearing at birth or arising during childhood. When symptomatic, EAH may be associated with hyperhidrosis or pain. We report a case of EAH on the calf of a young girl; review all other known documented cases in the literature; and summarize the clinical characteristics, histologic findings, and prognosis of this uncommon entity.[Abstract] [Full Text] [Related] [New Search]