Pregledni rad

Monostotic Fibrous Dysplasia of the Facial Bones

Marijo Bagatin ; Klinika za kirurgiju lica, čeljusti i usta Medicinskog i Stomatološkog fakulteta, Zagreb, Hrvatska
Spomenka Manojlović ; Zavod za opću i patološku anatomiju Medicinskog fakulteta, Zagreb, Hrvatska
Ivan Zajc ; Klinika za kirurgiju lica, čeljusti i usta Medicinskog i Stomatološkog fakulteta, Zagreb, Hrvatska
Vesna Čaćinović-Matić ; Zavod za opću i patološku anatomiju Medicinskog fakulteta, Zagreb, Hrvatska

Sažetak

Fibrous dysplasia is a rare condition in which a normal medullary bone is replaced by fibro-osseous tissue. The disorder is of unknown etiology and three forms of the disease have been recognized: monostotic fibrous dysplasia (MFD), polys to tic fibrous dysplasia (PFD) and Albright's syndrome (AS). A survey of 11 cases with monostotic fibrous dysplasia (MFD) of facial bones showed the maxilla to be more frequently affected (7) than the mandible (3), the sex ratio being approximately 1:1. Our patients confirmed that the disease to be encountered in all age groups, most often under the age o f 20. The swelling associated with functional disturbances is rare. The treatment of monostotic fibrous dysplasia is surgical and the procedure depends on the extent o f the lesion, limitation, consistency and age of the patient.

Ključne riječi

fibrous dysplasia; monostotic; jaws; facial bones

Hrčak ID:

99877

URI

https://hrcak.srce.hr/99877

Datum izdavanja:

15.3.1993.

Podaci na drugim jezicima: hrvatski

Posjeta: 8.201 *