Neurofibroma jẹ tumo afẹ-ara ti ko dara ninu eto aifọkanbalẹ agbeegbe. Ni 90% awọn iṣẹlẹ, wọn rii bi awọn èèmọ ti o duro nikan laisi eyikeyi awọn rudurudu jiini. Sibẹsibẹ, awọn iyokù ni a rii ni awọn eniyan ti o ni neurofibromatosis iru I (NF1), arun ti a jogun ti ara-ara-ara. Wọn le ja si ni ọpọlọpọ awọn aami aisan lati ibajẹ ti ara ati irora si ailera ailera.
Neurofibroma le jẹ 2 si 20 milimita ni iwọn ila opin, jẹ rirọ, alailara, ati Pinkish-funfun. A le lo biopsy fun ayẹwo histopathology.
Neurofibroma ni igbagbogbo dide ni awọn ọdun ọdọ ati nigbagbogbo wa lẹhin igbalagba. Ni awọn eniyan ti o ni Neurofibromatosis Iru I, wọn maa n tẹsiwaju lati pọ si ni nọmba ati iwọn ni gbogbo igba agbalagba.
A neurofibroma is a benign nerve-sheath tumor in the peripheral nervous system. In 90% of cases, they are found as stand-alone tumors, while the remainder are found in persons with neurofibromatosis type I (NF1), an autosomal-dominant genetically inherited disease. They can result in a range of symptoms from physical disfiguration and pain to cognitive disability.
☆ Ninu awọn abajade 2022 Stiftung Warentest lati Jẹmánì, itẹlọrun alabara pẹlu ModelDerm jẹ kekere diẹ ju pẹlu awọn ijumọsọrọ telemedicine isanwo.
Neurofibroma ti alaisan pẹlu neurofibromatosis.
Neurofibromas maa n buru si pẹlu ọjọ ori. Awọn egbo ninu ẹni kọọkan farahan ni akọkọ nigbati o jẹ ọdọ.
Neurofibromas jẹ awọn èèmọ alaiṣedeede ti o wọpọ ti a rii ni awọn ara agbeegbe. Wọn maa n dabi awọn gbigbo rirọ lori awọ ara tabi awọn odidi kekere labẹ rẹ. Wọn dagbasoke lati inu endoneurium ati awọn ara asopọ ti o wa ni ayika awọn apofẹlẹfẹlẹ ti agbeegbe. 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.
Neurofibroma le jẹ 2 si 20 milimita ni iwọn ila opin, jẹ rirọ, alailara, ati Pinkish-funfun. A le lo biopsy fun ayẹwo histopathology.
Neurofibroma ni igbagbogbo dide ni awọn ọdun ọdọ ati nigbagbogbo wa lẹhin igbalagba. Ni awọn eniyan ti o ni Neurofibromatosis Iru I, wọn maa n tẹsiwaju lati pọ si ni nọmba ati iwọn ni gbogbo igba agbalagba.