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Isolation and Characterization of Satellite Cells from Rat Head Branchiomeric Muscles
Published on: July 20, 2015
Diffuse idiopathic hyperplasia of the sternocleidomastoid muscle in a child
Kamalesh Pal1, Nisar Bhat, Khaled Moghazy
1Pediatric Surgery Division, Department of Surgery, King Fahad Hospital of University, Al-Khobar, Saudi Arabia. kamalesh_pal@yahoo.com
Abstract:
Unilateral diffuse or localized enlargement of the sternocleidomastoid muscle (SCM) is an event commonly seen in infancy, and is popularly known as 'sternocleidomastoid tumor'. The condition, which usually spontaneously resolves with or without physiotherapy, is due to a hematoma following a difficult labor. The muscle regains its elasticity and complete function. In some infants it resolves with fibromatous changes in the muscle leading to shortening, fibrosis and finally culminating in torticollis. We describe a case of idiopathic diffuse enlargement of unilateral SCM in a 12-year-old child without any functional compromise or torticollis. The histopathological and clinical characteristics differentiating it from more commonly described sternocleidomastoid tumor or fibromatosis coli are described. We believe this is the first case report of idiopathic hyperplasia of SCM.
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