Congenital smooth muscle hamartoma

Congenital smooth muscle hamartoma (CSMH) is a rare cutaneous hamartomatous lesion most often located on the lumbosacral area or proximal limbs (but rarely on atypical areas such as scalp, eyelid or foot) and characterized by a disorganized proliferation of smooth muscle fibres of arrector pili presenting usually as a localized skin-colored or hyperpigmented plaque (up to 10 cm in diameter) with prominent vellus hairs (most common classic form) or less commonly by multiple skin-colored papules that can coalesce to form irregularly shaped plaques. With time, hyperpigmentation and vellus hairs usually diminish and neither malignant transformation nor associated systemic involvement has been reported.

Melanocytic nevus

A oval and round, colored (usually medium-to dark brown, reddish brown, or flesh colored) lesion. Typically, a melanocytic nevus is less than 6 mm in diameter, but may be much smaller or larger.


Total: 1

                      


(per page)
PMID (PMCID)
16192884
MALE Infant
Congenital smooth muscle hamartoma: the importance of differentiation from melanocytic nevi.
Schmidt CS, Bentz ML.
J Craniofac Surg. 2005;16(5):926-9.
Congenital smooth muscle hamartoma: the importance of differentiation from melanocytic nevi.