A neurofibroma is a benign nerve-sheath tumor in the peripheral nervous system. In 90% of cases, they are found as stand-alone tumors, while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease. They can result in a range of symptoms from physical disfiguration and pain to cognitive disability.
☆ AI Dermatology — Free Service Natiijooyinka Stiftung Warentest ee 2022 ee ka yimid Jarmalka, ku qanacsanaanta macaamilka ee ModelDerm ayaa waxyar uun ka hooseysay la-talinta telemedicine-ka ee lacagta lagu bixiyo.
Neurofibroma ee bukaanka qaba neurofibromatosis.
Neurofibromas waxay u muuqdaan inay ka sii daraan da'da. Nabarrada qofkan ayaa markii ugu horreysay soo shaac baxay markuu yaraa.
Neurofibroma keli ah — papule jilicsan oo casaanka ah.
Neurofibromas waa burooyin aan waxyeello lahayn oo caadi ah oo laga helo neerfayaasha durugsan. Waxay caadi ahaan u eg yihiin papule jilicsan oo maqaarka ku yaal ama barar yar oo ka hooseeya. Waxay ka soo baxaan endoneurium iyo unugyada isku xiran ee ku wareegsan galaaska dareemayaasha durugsan. Neurofibromas are the most prevalent benign peripheral nerve sheath tumor. Often appearing as a soft, skin-colored papule or small subcutaneous nodule, they arise from endoneurium and the connective tissues of peripheral nerve sheaths.
Neurofibroma wuxuu noqon karaa dhexroor 2 ilaa 20 mm, waa jilicsan, dabacsan, iyo casaan‑cad. Biopsi ayaa loo isticmaali karaa ogaanshaha histopathology.
Neurofibroma caadi ahaan waxay soo baxaan sanadaha teenage‑ka waxayna badanaa dhacaan qaangaarnimada ka dib. Dadka qaba Neurofibromatosis Nooca I, waxay u muuqdaan inay sii wadaan inay kordhiyaan tirada iyo xajmiga inta ay qaangaarayaan.