Results 61 to 70 of about 12,175 (184)

Solitary neurofibroma of the inferior orbit: A rare occurrence

open access: yesMuller Journal of Medical Sciences and Research, 2015
Solitary neurofibroma in the absence of neurofibromatosis is of rare occurrence and very few have been reported in the literature till now especially in the inferior orbit. A case of solitary neurofibroma of the inferior orbit is presented here.
V Sowmya   +3 more
doaj   +1 more source

A Rare Case of Diffuse Extra‐Cranial Schwannomatosis of the Trunk and Limbs

open access: yesClinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Schwannomas are benign peripheral nerve sheath tumors (PNSTs) arising from myelin sheaths, with schwannomatosis characterized by multiple lesions without neurofibromatosis type 1 (NF1) or type 2 (NF2) stigmata. Malignant transformation is rare but documented.
Bernadette Pedun   +5 more
wiley   +1 more source

Chemokine receptor CCR3 is important for migration of mast cells in neurofibroma

open access: yesDermatologica Sinica, 2010
Background: Neurofibroma consists of abundant extracellular matrix and many types of cells, including Schwann cells (SCs), mast cells (MCs), fibroblasts and endothelial cells.
Wei-Chun Tai   +4 more
doaj   +1 more source

Pacinian neurofibroma [PDF]

open access: yesCancer, 1952
R W, PRICHARD, R P, CUSTER
openaire   +2 more sources

Solitary eyelid neurofibroma presenting as tarsal cyst: Report of a case and review of literature

open access: yesAmerican Journal of Ophthalmology Case Reports, 2018
Purpose: To report a rare case of solitary eyelid neurofiboma presenting as tarsal cyst. Observation: A 64 year old male, presented with a painless, non progressive swelling in the right upper eye lid.
Nisar Sonam Poonam   +3 more
doaj   +1 more source

Neurofibroma subungueal solitário: relato de um caso inédito no sexo masculino Solitary subungual neurofibroma: a previously unreported finding in a male patient

open access: yesAnais Brasileiros de Dermatologia, 2011
Neurofibroma é uma proliferação hamartomatosa de origem neuromesenquimal. Pode ser encontrado associado à neurofibromatose ou como tumor solitário, sendo sua apresentação subungueal solitária bastante rara.
Dionne de Almeida Stolarczuk   +4 more
doaj   +1 more source

Distinctive mesenchymal-like neurofibroma stem cells shape NF1 clinical phenotypes controlled by BDNF microenvironment

open access: yesTranslational Oncology
Background: Neurofibroma type I (NF1) often presents with multiple clinical phenotypes due to mutations of NF1 gene. The aim of this study was to determine the phenotypic and therapeutic relevance of tumor microenvironment in NF1 patients. Methods: Tumor
Jingcun Shi   +9 more
doaj   +1 more source

Neurofibroma: Case Series with Clinical Features and Recommendations

open access: yesActa Neurologica Taiwanica
Neurofibroma is an autosomal benign disorder. It can be localized, diffuse or invasive like plexiform neurofibroma that involves the nerves, muscle, tissues, skeleton.
Nasreen Khatri   +5 more
doaj  

A Giant Scrotal Neurofibroma in a Child Masquerading as Filariasis: Uncommon Presentation of a Common Disease

open access: yesPrague Medical Report
Neurofibroma of the scrotum is a very uncommon benign neoplasm, specifically when it affects teenagers and is not associated with neurofibromatosis type I.
Anurag Singh   +3 more
doaj   +1 more source

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