Neurofibromahttps://en.wikipedia.org/wiki/Neurofibroma
Neurofibroma i-benign nerve-sheath bundu iri paripheral nervous system. Mu90% yezviitiko, ivo vanowanikwa semamota akamira ega pasina chero genetic disorder. Zvisinei, zvakasara zvinowanikwa muvanhu vane neurofibromatosis type I (NF1), chirwere che autosomal-dominant genetically nhaka. Vanogona kuguma nehuwandu hwezviratidzo kubva pakukanganiswa kwemuviri uye kurwadziwa kusvika pakuremara kwekuziva.

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

Neurofibroma kazhinji inomuka mumakore ekuyaruka uye kazhinji mushure mekuyaruka. Muvanhu vane Neurofibromatosis Type I, vanowanzo ramba vachiwedzera nhamba uye saizi mukukura kwese.

☆ Mune 2022 Stiftung Warentest mhedzisiro kubva kuGermany, kugutsikana kwevatengi neModelDerm kwakangodzikira zvishoma pane nekubhadharwa kwe telemedicine kubvunzana.
  • Neurofibroma yemurwere ane neurofibromatosis.
  • Neurofibromas inowanzowedzera nezera. Maronda emunhu uyu akatanga kuonekwa achiri mudiki.
  • Solitary neurofibroma ― A soft erythematous papule.
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.