Neurofibroma shine tumor mara cuta na jijiyoyin sheath a cikin tsarin jijiyoyin gefe. A cikin kashi 90% na lokuta, ana samun su azaman ƙwayoyin cuta masu zaman kansu ba tare da wata cuta ta kwayoyin halitta ba. Duk da haka, ana samun ragowar a cikin mutanen da ke da nau'in neurofibromatosis I (NF1), cuta mai gadon autosomal‑dominant. Suna iya haifar da kewayon alamun daga lalacewa ta jiki da zafi zuwa rashin hankali.
Neurofibroma na iya zama 2 zuwa 20 mm a diamita, mai laushi, mai sassauci, da ruwan hoda‑fari. Za a iya amfani da biopsy don ganewar asali na histopathology.
Neurofibroma yawanci yana tasowa a cikin shekarun samartaka kuma galibi bayan balaga. A cikin mutanen da ke dauke da neurofibromatosis nau'in I, suna ci gaba da karuwa a lamba da girma a duk lokacin balaga.
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.
Neurofibroma na marasa lafiya tare da neurofibromatosis.
Neurofibromas yakan tsananta da shekaru. Raunin da ke cikin wannan mutum ya fara bayyana lokacin yana matashi.
Neurofibromas sune ciwace-ciwacen da ake samu a jijiyoyi na gefe. Yawanci suna kama da dunƙule masu laushi akan fata ko ƙananan dunƙule a ƙarƙashinsa. Suna tasowa daga endoneurium da kyallen jikin da ke kewaye da sheaths na jijiya. 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 na iya zama 2 zuwa 20 mm a diamita, mai laushi, mai sassauci, da ruwan hoda‑fari. Za a iya amfani da biopsy don ganewar asali na histopathology.
Neurofibroma yawanci yana tasowa a cikin shekarun samartaka kuma galibi bayan balaga. A cikin mutanen da ke dauke da neurofibromatosis nau'in I, suna ci gaba da karuwa a lamba da girma a duk lokacin balaga.