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Title:Infantile myofibromathosis of the maxilla. A case report
Authors:ID Ihan Hren, Nataša (Author)
Files:.pdf PDF - Presentation file, download (145,86 KB)
MD5: D8E4809761ADA8DAAFD5326F6BC4E090
 
Language:English
Typology:1.04 - Professional Article
Organization:Logo OI - Institute of Oncology
Abstract:Background. Infantile myofibromatosis is a rare benign tumour in children. Itscharacteristic symptoms are firm masses in soft tissues, bones and visceralorgans, 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.
Publication status:Published
Publication version:Version of Record
Publication date:01.01.2002
Publisher:Slovenian Medical Association - Slovenian Association of Radiology, Nuclear Medicine Society, Slovenian Society far Radiotherapy and Oncology, and Slovenian Cancer Society
Year of publishing:2002
Number of pages:str. 47-51
Numbering:Letn. 36, št. 1
Source:Ljubljana
PID:20.500.12556/DiRROS-18034 New window
UDC:616-006
ISSN on article:1318-2099
COBISS.SI-ID:14748121 New window
Copyright:by Authors
Note:BSDOCID88063;
Publication date in DiRROS:31.01.2024
Views:539
Downloads:137
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IHAN HREN, Nataša, 2002, Infantile myofibromathosis of the maxilla. A case report. Radiology and oncology [online]. 2002. Vol. 36, no. 1, p. 47–51. [Accessed 6 April 2025]. Retrieved from: https://dirros.openscience.si/IzpisGradiva.php?lang=eng&id=18034
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Record is a part of a journal

Title:Radiology and oncology
Shortened title:Radiol. oncol.
Publisher:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 New window

Secondary language

Language:Slovenian
Title:Infantolna miofibromatoza maksile. Prikaz primera
Abstract:Izhodišča. Infantilna miofibromatoza je redek benigni tumor otrok. Značilne sočvrste 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.


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