Cranial infantile myofibromatosis: report of three cases

Citation
F. Soylemezoglu et al., Cranial infantile myofibromatosis: report of three cases, CHILD NERV, 17(9), 2001, pp. 524-527
Citations number
23
Categorie Soggetti
Pediatrics
Journal title
CHILDS NERVOUS SYSTEM
ISSN journal
02567040 → ACNP
Volume
17
Issue
9
Year of publication
2001
Pages
524 - 527
Database
ISI
SICI code
0256-7040(200109)17:9<524:CIMROT>2.0.ZU;2-R
Abstract
Background: Infantile myofibromatosis is a proliferative disorder of infanc y and early childhood characterized by the development of single or multipl e nodular lesions arising from cutaneous or subcutaneous tissue, muscle, bo ne or visceral organs. In approximately one-third of cases, this myofibrobl astic proliferation involves the head and neck region. Case report: In this paper we report on three cases of cranial infantile my ofibromatosis in infants. The clinical presentation and the deceptive histo pathological features can make diagnosis difficult. Conclusion: The significance of recognizing this entity is stressed, since its indolent clinical behavior might prevent diagnosis.