SciELO - Scientific Electronic Library Online

vol.78 issue4Albopapuloid epidermolysis bullosa (Pasini's variant)Mosaic epidermolytic hyperkeratosis author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand




Related links


Anais Brasileiros de Dermatologia

Print version ISSN 0365-0596On-line version ISSN 1806-4841


LISE, Michelle Larissa Zini et al. Eccrine angiomatous hamartoma: a painful tumor. An. Bras. Dermatol. [online]. 2003, vol.78, n.4, pp.465-474. ISSN 0365-0596.

Eccrine angiomatous hamartoma (EAH) is a benign lesion usually present at birth. In most cases it presents as a flesh-colored or erythematous nodule or patch. It may or may not be associated with focal hyperhydrosis and pain. It is most commonly located in the lower extremities, near the knee or on the toes, but lesions on the face, sacral and cervical region and trunk have been described. The main differential diagnosis should be made with a glomus tumor. In general, EAH shows benign behavior, and spontaneous remission of pain has been described. Cases have been reported in which the pain led to excision and even to amputation of the affected member. The authors present a case of late onset EAH, with exuberant symptoms, which was difficult to treat.

Keywords : pain; hamartoma; hyperhydrosis; nevus.

        · abstract in Portuguese     · text in Portuguese     · Portuguese ( pdf epdf )


Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License