Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Ko te Neurofibroma he tumour o te pūngao nerve‑sheath (nerve‑sheath tumour) i roto i te punaha pūngao tawhiti (peripheral nervous system). I roto i te 90 % o ngā kēti, ka kitea he pukupuku tū motuhake kāore he mate ira. Engari, ko te toenga ka kitea i roto i ngā tangata whai neurofibromatosis type I (NF1), he mate tuku iho autosomal‑dominant (autosomal‑dominant inherited disorder). Ka puta he maha o ngā tohu mai i te āhua kino o te tinana me te māmae ki te hauatanga hinengaro.

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

Neurofibroma ka ara ake i roto i ngā tau o te taiohi, ka mutu i muri i te pakeketanga. I ngā tangata whai neurofibromatosis type I, ka piki haere tonu te maha me te rahi puta noa i te pakeketanga.

☆ 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 whero (erythematous papule).
References Neurofibroma 30969529 
NIH
Ko te Neurofibromas he pukupuku ngawari noa e kitea ana i roto i nga nerve peripheral (peripheral nerves). 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 (peripheral nerves).
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.