Rl. Sulica et al., ECCRINE ANGIOMATOUS HAMARTOMA (NEVUS) - IMMUNOHISTOCHEMICAL FINDINGS AND REVIEW OF THE LITERATURE, Journal of cutaneous pathology, 21(1), 1994, pp. 71-75
Eccrine angiomatous hamartoma (nevus) is a rare form of congenital tum
orous malformation with proliferation of eccrine secretory coils and d
ucts, surrounding capillary angiomatous channels and occasionally othe
r minor elements. To date, there have been only about 24 cases reporte
d in the literature. We report an additional case with more detailed d
escription of the microscopic findings, including immunohistochemical
observations. The patient was a 28-year-old female who presented with
painless, flesh- to reddish brown-colored, violaceous or bluish subcut
aneous nodules on the extremities and trunk. The tumors did not show s
weating following exertion. The histologic features were comparable to
the previously reported cases. The hamartomatous eccrine sweat glands
and ducts and a few apocrine glands demonstrated qualitatively dimini
shed antigens commonly found in the eccrine sweat apparatuses, such as
carcinoembryonic antigen (CEA) and S-100 protein. The findings of CD3
4, CD44, human nerve growth factor receptor and Ulex europaeus antigen
s have not been previously reported. The histologic features suggested
a ''hamartomatous'' growth rather than a true neoplastic process.