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.
Neurofibromas yizimila ezingenabungozi ezivamile ezitholakala emithanjeni ye-peripheral. Ngokuvamile abukeka njengamaqhubu athambile esikhumbeni noma amaqhubu amancane ngaphansi kwaso. Zikhula zisuka ku-endoneurium kanye nezicubu ezixhumeneyo ezizungeze i-peripheral nerve sheaths. 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.
i-neurofibroma (neurofibroma) ingase ibe ngu-2 kuya ku-20 mm ububanzi, ithambile, i-flaccid, futhi imhlophe ngokubomvana. I-biopsy ingasetshenziselwa ukuxilongwa kwe-histopathology.
i-neurofibroma (neurofibroma) ngokuvamile ivela eminyakeni yobusha futhi ngokuvamile ngemva kokuthomba. Kubantu abane-Neurofibromatosis Type I, bathambekele ekuqhubekeni banda ngenani nangosayizi phakathi kwabantu abadala.