This Article  • Full text  • PDF  • Reply to article  • Send to a friend  • Save in My Folder  • Save to citation manager  • Permissions  Citing Articles  • Contact me when this article is cited  Related Content  • Related article  • Similar articles in this journal  Topic Collections  • Pathology of Head & Neck  • Pediatric Otolaryngology  • Diagnosis  • Alert me on articles by topic  Social Bookmarking   What's this?

Arch Otolaryngol Head Neck Surg. 2007;133(6):622-623.

	Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Diagnosis: Infantile myofibromatosis

Myofibromas are rare fibrous tumors that most commonly affect infants and young children. Typical lesions are firm or rubbery and usually present as a solitary mass or as multiple nodules with or without visceral involvement. Solitary lesions have a predilection for the head and neck (36%) and trunk (33%) and can appear in skin, muscle, subcutaneous tissue, and bone.¹ While individual tumors can present at any age, approximately 50% of solitary lesions are present at birth and more than 75% emerge before 12 months of age.^1-2 There also appears to be a predilection for boys (male-female ratio, 2:1).¹ Despite being rare overall, myofibroma is the most common fibrous tumor of infancy and childhood^2-4 and should therefore be considered in any child with a nodular growth in the head and neck region. Within the head and neck, myofibroma has been documented in the scalp, forehead, orbit, oral cavity, larynx, parotid gland, . . . [Full Text of this Article]

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter     What's this?

RELATED ARTICLE

Pathology Quiz Case 1
Justin Turner, Margaret Skinner, Michael J. Caplan, and M. Boyd Gillespie
Arch Otolaryngol Head Neck Surg. 2007;133(6):620.
EXTRACT | FULL TEXT