Eccrine angiomatous hamartoma, a rare entity
DOI:
https://doi.org/10.29176/2590843X.1808Keywords:
Eccrine glands, Hamartoma/Congenital, Hamartoma, Neoplasms, Vascular tissueAbstract
Angiomatous eccrine hamartoma is characterized by a proliferation of multiple eccrine and vascular structures, generally presenting from birth, with growth proportional to the individual; as solitary or multiple plaques or nodules of variable color that mainly affect the distal extremities. The exact pathogenesis is unknown, but several theories have been proposed, including abnormal heterotypic dependency induction with resulting malformation of adnexal and mesenchymal elements. The diagnosis must be confirmed with the histopathological study, where a neoplasm in the middle or deep dermis with proliferation of eccrine glands and vascular structures will be found. For symptomatic patients surgical excision is the treatment.
Author Biographies
Jennifer Arenas Sepúlveda, Universidad de Antioquia
Departamento de Dermatología, Universidad de Antioquia, Centro de Investigaciones Dermatológicas (CIDERM).
Luis Alfonso Correa-Londoño, Universidad de Antioquia
Docente de Dermatopatología, Sección de Dermatología, Facultad de Medicina, Universidad de Antioquia.
Maria Natalia MejíaBarreneche, Universidad de Antioquia
Médica dermatóloga. Docente, Sección de Dermatología, Facultad de Medicina, Universidad de Antioquia.
Laura Andrea Peña-Mejía, Universidad de Antioquia
Residente de Patología, Facultad de Medicina, Universidad de Antioquia.
References
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