Avtor/Urednik		Ihan-Hren, Nataša
Naslov		Infantile myofibromathosis of the maxilla. A case report
Prevedeni naslov		Infantolna miofibromatoza maksile. Prikaz primera
Tip		članek
Vir		Radiol Oncol
Vol. in št.		Letnik 36, št. 1
Leto izdaje		2002
Obseg		str. 47-51
Jezik		eng
Abstrakt		Background. Infantile myofibromatosis is a rare benign tumour in children. Its characteristic symptoms are firm masses in soft tissues, bones and visceral organs, and its common locations are head and neck. Three forms are well known: solitary, multicentric and visceral myofibromatosis. All have excellent prognosis, except the last one that may be lethal. Spontaneous regression can occur. Case report. We present an unusual case of infantile myofibromatosis of the maxilla in an adolescent. Conclusions. The infantile myofibromatosis should be managed with special caution because of the differential-diagnostic similarity with fibrosarcoma, leomyosarcoma, and histiocytosis.
Izvleček		Izhodišča. Infantilna miofibromatoza je redek benigni tumor otrok. Značilne so čvrste mase v mehkih tkivih, kosteh ali notranjih organih. Pogosto se pojavlja na glavi in vratu. Poznane so tri oblike: solitarna, multicentrična in visceralna miofibromatoza. Zadnja oblika je lahko smrtna, ostale imajo odlično prognozo. Znana je spontana regresija. Prikaz primera. Opisan je manj značilen primer najstnika z obsežno solitarno miofibromatozo zgornje čeljustnice. Zaključki. Pri diagnosticiranju infantilne miofibromatoze je potrebna posebna pozornost zaradi diferencialno diagnostične podobnosti s fibrosarkomom, leomiosarkomom, histiocitozo.
Deskriptorji		MYOFIBROMATOSIS MAXILLARY NEOPLASMS CHILD