Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Ko te Neurofibroma he puku o te pūpē pūngao i roto i te pūnaha pūngao pūngao. I roto i te 90 % o ngā kēhi, ka kitea he pukupuku motuhake kāore he mate i te wā. Engari, ka kitea te toenga i roto i ngā tāngata whai Neurofibromatosis momo I (NF1), he mate tuku iho autosomal. Ka puta he maha o ngā tohu, pēnei i te āhua kino o te tinana me te mamae ki te hauatanga hinengaro.

He Neurofibroma ka rahi 2 ki te 20 mm te whānui, he ngohe, he māwhero, he māwhero‑ma. Ka taea te whakamahi i te biopsy mō te tātaritanga histopathology.

Ka ara ake te Neurofibroma i roto i ngā tau o te taiohi, ka mutu i muri i te pakeketanga. I ngā tāngata whai Neurofibromatosis Momo I, ka piki haere tonu te maha me te rahi puta noa i te pakeketanga.

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  • He neurofibroma o te manawanui, e pā ana ki te neurofibromatosis.
  • Neurofibromas ka kaha haere i te wā o te pakeke. I puta tuatahi ngā mate o tēnei tangata i te wā e tāihoia ana ia.
  • Solitary neurofibroma – He papule whero, ngawari.
References Neurofibroma 30969529 
NIH
Ko te Neurofibromas he pukupuku ngawari noa e kitea ana i roto i ngā nerve peripheral. He rite tonu te āhua ki ngā putunga ngawari i runga i te kiri, i ngā putunga iti rānei kei raro iho. Ka puta mai i te endoneurium me ngā kopa hono e karapoti ana i ngā 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.