Neurofibroma ndi chotupa chosaopsa cha mitsempha mumtsempha wa mitsempha. Mu 90% ya milandu, amapezeka ngati zotupa zokha popanda vuto lililonse la majini. Komabe, zotsalazo zimapezeka mwa anthu omwe ali ndi neurofibromatosis mtundu I (NF1), matenda otengera majini omwe amatengera autosomal. Zingayambitse zizindikiro zosiyanasiyana kuchokera ku kuwonongeka kwa thupi ndi ululu mpaka kulumala kwa chidziwitso.
Neurofibroma ikhoza kukhala 2 mpaka 20 mm m'mimba mwake, ndi yofewa, yosalala, ndi yoyera ngati pinki. Biopsy angagwiritsidwe ntchito kufufuza histopathology.
Neurofibroma nthawi zambiri amawonekera m'zaka zaunyamata ndipo nthawi zambiri amatha kutha msinkhu. Mwa anthu omwe ali ndi Neurofibromatosis Type I, amakonda kupitiliza kuchuluka ndi kukula muukulu wonse.
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 ya wodwala neurofibromatosis.
Neurofibromas imakonda kukulirakulira ndi ukalamba. Zilonda za munthu uyu zidawonekera koyamba ali wachinyamata.
Solitary neurofibroma ― Papule yofewa ya yotsekeka (erythematous).
Neurofibromas ndi zotupa zoyipa zomwe zimapezeka m'mitsempha yozungulira. Amawoneka ngati totupa tofewa pakhungu kapena zotupa zazing'ono pansi pake. Amapangidwa kuchokera ku endoneurium ndi minyewa yolumikizana yozungulira zotumphukira zamitsempha. 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 ikhoza kukhala 2 mpaka 20 mm m'mimba mwake, ndi yofewa, yosalala, ndi yoyera ngati pinki. Biopsy angagwiritsidwe ntchito kufufuza histopathology.
Neurofibroma nthawi zambiri amawonekera m'zaka zaunyamata ndipo nthawi zambiri amatha kutha msinkhu. Mwa anthu omwe ali ndi Neurofibromatosis Type I, amakonda kupitiliza kuchuluka ndi kukula muukulu wonse.