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.
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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.