Results 21 to 30 of about 20,018 (209)
A case of two sporadic cellular neurofibromas with atypia and one widespread hyalinization neurofibroma of the lumbar spine in a 51-year-old man without evidence of neurofibromatosis-1 is reported. Cellular neurofibroma with atypia is an unusual variant.
Shih-Wen Hu +3 more
doaj +1 more source
Solitary intraosseous neurofibroma of the mandible. Apropos of a case [PDF]
Neurofibroma is a benign neoplasm derived from peripheral nerves. Most of these are associated with Neurofibromatosis but may also occur as solitary lesions. When found on the head and neck they are generally located in the soft tissue.
Deichler, Javiera +5 more
core +1 more source
Genetically engineered minipigs model the major clinical features of human neurofibromatosis type 1. [PDF]
Neurofibromatosis Type 1 (NF1) is a genetic disease caused by mutations in Neurofibromin 1 (NF1). NF1 patients present with a variety of clinical manifestations and are predisposed to cancer development.
Carlson, Daniel F +21 more
core +2 more sources
Pigmented neurofibroma of the skin
Pigmented neurofibroma is a rare variant of neurofibroma commonly associated with neurofibromatosis 1 of diffuse type. Histopathologic examination is essential to differentiate it from other pigmented lesions.
Hemalata Mahantappa +2 more
doaj +1 more source
Voice characteristics in adults with neurofibromatosis type 1 [PDF]
Introduction and aims of the study: Change or loss of voice in patients with neurofibromatosis type 1 (NF1) has been associated with head and neck neurofibromas.
Corthals, Paul +4 more
core +2 more sources
Cutaneous Neurofibroma of the Lacrimal Caruncule: A Case Report
We describe the case of a neurofibroma on the lacrimal caruncle of a female patient with neurofibromatosis type 1 (NF1). NF1 is an autosomal dominant genetic disease with a wide variety of clinical manifestations, one of the most common of which is ...
Mario Motta, Mauro Geller, Cesar Motta
doaj +1 more source
Pigmented neurofibroma with hypertrichosis
Background: Pigmented (or melanocytic) neurofibroma (PN) constitutes only 1% of cases and is considered a rare variant of neurofibroma containing melanin-producing cells. In addition, the association of PN with hypertrichosis is infrequent.
Juan A. Godínez-Chaparro +6 more
doaj +1 more source
Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report [PDF]
Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. The diagnosis of Neurofibromatosis type 1 is not dilemmatic because of typical clinical features.
Gogineni, Subhas Babu +1 more
core +1 more source
Accuracy of mobile digital teledermoscopy for skin self-examinations in adults at high risk of skin cancer: an open-label, randomised controlled trial [PDF]
Background: Skin self-examinations supplemented with mobile teledermoscopy might improve early detection of skin cancers compared with naked-eye skin self-examinations.
Avilés-Izquierdo +25 more
core +1 more source
Revisiting the NPcis mouse model: A new tool to model plexiform neurofibroma.
Neurofibromatosis Type I (NF1) is a rare genetic disorder. NF1 patients frequently develop a benign tumor in peripheral nerve plexuses called plexiform neurofibroma.
Camille Plante +9 more
doaj +1 more source

