Neurofibroma shine ciwon kumburin jijiyoyi mara kyau a cikin tsarin jijiya na gefe. A cikin kashi 90% na lokuta, ana samun su azaman ciwace-ciwacen ciwace-ciwace 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 gada ta autosomal. Suna iya haifar da kewayon alamun bayyanar cututtuka daga lalacewa ta jiki da zafi zuwa rashin hankali.
Neurofibroma na iya zama 2 zuwa 20 mm a diamita, mai laushi, mai laushi, 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, sun kasance suna ci gaba da karuwa a lamba da girma a duk lokacin girma.
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.
☆ A cikin sakamakon Stiftung Warentest na 2022 daga Jamus, gamsuwar mabukaci tare da ModelDerm ya ɗan yi ƙasa kaɗan fiye da biyan shawarwarin telemedicine.
Neurofibroma na marasa lafiya tare da neurofibromatosis.
Neurofibromas yakan tsananta da shekaru. Raunin da ke cikin wannan mutum ya fara bayyana lokacin yana matashi.
Solitary neurofibroma ― Papule mai laushi mai laushi.
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 laushi, 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, sun kasance suna ci gaba da karuwa a lamba da girma a duk lokacin girma.