Eccrine angiomatous hamartoma in a neurofibromatosis type-1 patient

Multiple and Familial Eccrine Angiomatous Hamartoma

“…The immunohistochemical analysis of EAH has only been carried out in a few recent cases (11)(12)(13)(14). As in normal eccrine glands, the secretory portion of the eccrine glands is positive for S100, carcinoembryogenic antigen (CEA), epithelial membrane antigen (EMA) and Cam5.2.…”

Eccrine naevus with clear cell syringoma

“…It is very unusual for an eccrine naevus to present as an erythematous papule in the lower eyelid as in this case, although various clinical manifestations have been described such as papules in a linear distribution, depressed patches, a solitary sweat‐discharging pore type and asymptomatic papule or polypoid lesion without sweat increase 1,2 . Moreover, our case is the first report of eccrine naevus associated with other diseases, although eccrine angiomatous hamartoma with type I neurofibromatosis had been reported 3 …”

Eccrine angiomatous hamartoma: Late onset facial presentation

“…[10] This helped us to differentiate the lesion from tufted angioma and other vascular malformations. Lesional hypertrichosis and the association of EAH with Cowden's syndrome,[11] neurofibromatosis,[12] etc., have all been reported.…”