Neurofibroma est tumor benignus nervi peripheralis. In 90 % casuum soli tumores, sine ulla perturbatione genetica, reperiuntur. Reliquae tamen in personis cum generis I (NF1, neurofibromatosis) reperiuntur, hereditate autosomali dominanti. Possunt manifestari variis signis, inter deformitates corporis, dolorem, et defectus cognitivos.
Neurofibroma typice habet diametrum 2–20 mm, est molle, flaccidum, et albido‑reniforme. Biopsia adhiberi potest ad diagnosis histopathologicam.
Neurofibroma saepe in adolescens aetate oritur et plerumque post pubertatem apparens. In hominibus cum Neurofibromatosis Type I, numerus et magnitudo tumorum per aetatem augentur.
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.
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Neurofibroma patientis cum neurofibromatosis.
Neurofibromas aetate peior fit. Laesiones in hoc individuo primum apparuerunt cum erat teenager.
Neurofibromas communes benigni tumores in nervis periphericis inveniri possunt. Plerumque mollis in cute se manifestat vel parvas massas sub cutis observare licet. Evolvunt ex endoneuro et tela connectiva circum nervum periphericum. 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 typice habet diametrum 2–20 mm, est molle, flaccidum, et albido‑reniforme. Biopsia adhiberi potest ad diagnosis histopathologicam.
Neurofibroma saepe in adolescens aetate oritur et plerumque post pubertatem apparens. In hominibus cum Neurofibromatosis Type I, numerus et magnitudo tumorum per aetatem augentur.