Ko te Neurofibroma he puku nerve-sheath pai i roto i te punaha nerve peripheral. I roto i te 90% o nga keehi, ka kitea he pukupuku tu motuhake kaore he mate ira. Engari, ko te toenga ka kitea i roto i nga tangata whai neurofibromatosis momo I (NF1), he mate tuku iho ira-autosomal. Ka puta he maha o nga tohu mai i te ahua kino o te tinana me te mamae ki te hauatanga hinengaro.
Neurofibroma pea 2 ki te 20 mm te whanui, he ngohe, he mawhero, he mawhero-ma. Ka taea te whakamahi he biopsy mo te tātaritanga histopathology.
Neurofibroma ka ara ake i roto i nga tau o te taiohi, ka mutu i muri i te pakeketanga. I nga tangata whai Neurofibromatosis Momo I, ka piki haere tonu te maha me te rahi puta noa i te pakeketanga.
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.
☆ I te 2022 Stiftung Warentest hua mai i Tiamana, he iti noa iho te pai o nga kaihoko ki a ModelDerm i nga korero mo te waea rongoa utu.
Neurofibroma o te manawanui ki te neurofibromatosis.
Neurofibromas ka kaha haere i te wa o te pakeke. I puta tuatahi nga mate o tenei tangata i te wa e taiohi ana ia.
Solitary neurofibroma ― He papule erythematous ngawari.
Ko te Neurofibromas he pukupuku ngawari noa e kitea ana i roto i nga nerves peripheral. He rite tonu te ahua ki nga putunga ngawari i runga i te kiri, i nga putunga iti ranei kei raro iho. Ka puta mai i te endoneurium me nga kopa hono e karapoti ana i nga kohanga nerve peripheral. 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 pea 2 ki te 20 mm te whanui, he ngohe, he mawhero, he mawhero-ma. Ka taea te whakamahi he biopsy mo te tātaritanga histopathology.
Neurofibroma ka ara ake i roto i nga tau o te taiohi, ka mutu i muri i te pakeketanga. I nga tangata whai Neurofibromatosis Momo I, ka piki haere tonu te maha me te rahi puta noa i te pakeketanga.