Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Neurofibroma i‑benign nerve‑sheath tumor (tumor) iri peripheral nervous system. Muzana 90% yezviitiko, ivo vanowanikwa sezvinyorwa zvoga pasina chero genetic disorder. Zvisinei, zvakasara zvinowanikwa muvanhu vane neurofibromatosis type I (NF1), chirwere che autosomal‑dominant chinotapuriranwa nemhuri. Vanogona kuguma nehuwandu hwezviratidzo kubva pakukanganiswa kwemuviri uye kurwadziwa kusvika pakurema kwepfungwa (cognitive impairment).

Neurofibroma inogona kunge iri 2 kusvika 20 mm mudiameter, yakapfava, uye pinki chena. Biopsy inogona kushandiswa kuongorora histopathology.

Neurofibroma kazhinji inomuka mumakore ekuyaruka, kazhinji mushure mekuyaruka. Muvanhu vane Neurofibromatosis Type I, vanowanzo kuwedzera huwandu uye saizi mukukura kwese.

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  • Neurofibroma yemurwere ane neurofibromatosis.
  • Neurofibromas inowanzowedzera nezera. Maronda emunhu uyu akatanga kuonekwa achiri mudiki.
  • Neurofibroma imwechete ― papula yakapfava inotsvuka.
References Neurofibroma 30969529 
NIH
Neurofibromas ndiwo ajairika benign tumors anowanikwa mumaperipheral nerves. Anowanzoita semapundu akapfava paganda kana mapundu madiki pasi payo. Dzinokura kubva ku endoneurium uye matishu anobatanidza akatenderedza 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.