Results 21 to 30 of about 20,018 (209)

Cellular Neurofibroma with Atypia Mimics Sarcoma: Report of a Case with Immunohistochemical Staining Pattern Analysis and Literature Review

open access: yesKaohsiung Journal of Medical Sciences, 2006
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]

open access: yes, 2011
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]

open access: yes, 2018
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

open access: yesArchives of Medicine and Health Sciences, 2015
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]

open access: yes, 2010
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

open access: yesCase Reports in Ophthalmology, 2017
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

open access: yesBoletín Médico del Hospital Infantil de México, 2023
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]

open access: yes, 2011
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]

open access: yes, 2020
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.

open access: yesPLoS ONE
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

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