Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Neurofibroma i‑benign nerve‑sheath bundle iri mu peripheral nervous system. Muzana re90% yezviitiko, inowanikwa semahombekombe akamira ega pasina chero genetic disorder. Zvisinei, inowanikwa muvanhu vane Neurofibromatosis type I (NF1), chirwere che autosomal‑dominant genetically nhaka. Vanogona kuve nezviratidzo zvakawanda, kubva pakukanganiswa kwemuviri, kurwadziwa, kusvika pakuremara kwekuziva.

Neurofibroma inogona kunge iri 2 kusvika 20 mm muhupamhi, yakapfava, isina kusimba, uye yepingi‑chena. Biopsy inogona kushandiswa kuongorora histopathology.

Neurofibroma kazhinji inowanikwa mumakore ekuyaruka uye inowanzobuda mushure mekuyaruka. Muvanhu vane Neurofibromatosis Type I, vanowanzoenderera mberi nekuwedzera nhamba uye saizi panguva yekukura kwese.

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  • Neurofibroma yemurwere ane neurofibromatosis.
  • Neurofibromas inowanzowedzera nekukura kwemunhu. Maronda aya akatanga kuoneka achiri mudiki.
  • Neurofibroma imwechete ― papula yakapfava, inoratidza ruvara rutsvuku.
References Neurofibroma 30969529 
NIH
Neurofibromas ndiwo ajairika benign tumors anowanikwa mumaperipheral nerves. Anowanzoita semapundu akapfava paganda kana mapundu madiki pasi peganda. 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.