Results 1 to 10 of about 12,175 (184)

Neurofibroma of the Palate [PDF]

open access: yesCase Reports in Dentistry, 2014
Neurofibroma is a benign peripheral nerve sheath tumor comprising variable mixture of Schwann cells, perineurial-like cells, and fibroblasts. Neurofibroma may occur as solitary lesion or as part of a generalised syndrome of neurofibromatosis or very ...
Tirumalasetty Sreenivasa Bharath   +5 more
doaj   +3 more sources

Proof-of-principle of NF1 gene therapy in plexiform neurofibroma xenograft mouse models [PDF]

open access: yesCommunications Biology
Neurofibromatosis type I is a rare neurocutaneous syndrome characterized by the development of disfiguring neurofibroma tumors with unmet clinical needs.
Dhanushka Hewa Bostanthirige   +11 more
doaj   +2 more sources

Neurofibroma of the Lingual Nerve: A Case Report

open access: yesKaohsiung Journal of Medical Sciences, 2006
A neurofibroma of the lingual nerve is a rare clinical finding, the most common lesion site of a lingual neurofibroma being the tongue. In most situations, it is difficult to determine the precise nerve origins.
Hsun-Mo Wang   +4 more
exaly   +3 more sources

Human cutaneous neurofibroma matrisome revealed by single-cell RNA sequencing

open access: yesActa Neuropathologica Communications, 2021
Neurofibromatosis Type I (NF1) is a neurocutaneous genetic syndrome characterized by a wide spectrum of clinical presentations, including benign peripheral nerve sheath tumor called neurofibroma.
Jean-Philippe Brosseau   +6 more
doaj   +1 more source

A case report of a 4-year-old girl with neurofibromatosis type 1

open access: yesCancer Treatment and Research Communications, 2022
Neurofibromatosis type 1 is a rare genetic disorder, which is a benign nerve tumor resulting from aberrant growth of the cells of nerve sheath. NF1 patients were associated with multisystem involvement, characterized by neurofibroma, of which 50% were ...
Mengying Peng, Yuqing Zhang, Qiong Zhou
doaj   +1 more source

An Unusual Presentation of Neurofibroma Masquerading as a Vascular Hamartoma, Post-Iatrogenic Intervention [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Neurofibroma is a localized discrete mass of benign nerve sheath tumour in the peripheral nervous system. Mostly present as skin lesions. Solitary neurofibroma may occur in deep soft tissue or subcutaneous plane in rare cases associated with syndromes ...
Abhishek Mukesh Shah   +4 more
doaj   +1 more source

Mechanical Ptosis in Neurofibromatosis Type 1 Heralding the Diagnosis of Right Sided Cervical Vagus Nerve Neurofibroma: A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Neurofibromatosis type 1 (NF1) is an autosomal dominant, multisystem disorder. In NF1, involvement of vagus nerve can occur in the form of neurofibroma.
Jyotiranjan Mallick   +4 more
doaj   +1 more source

A case report of solitary neurofibroma of the Vas deferens

open access: yesUrology Case Reports, 2020
Solitary neurofibroma of the male genital tract is a rare benign peripheral nerve sheath tumor which is considered to originate from the Schwann cell. Neurofibroma of the male genital tract has been reported extremely rarely in the literature. We present
Abdullah, Jun-ping Xing
doaj   +1 more source

Intrascrotal Solitary Neurofibroma [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2020
A BSTRACT Solitary Neurofibroma of the scrotum is a rare benign tumour, particularly when it is not associated with neurofibromatosis Type I, hence, less number of cases have been reported in the English literature.
Abhishek Gupta, Suhas N Jajoo
doaj   +1 more source

Histopathological Variants of Cutaneous Neurofibroma: A Compendious Review

open access: yesDermatopathology, 2022
The first description of histopathological variants of neurofibroma dates back to 1994. Over the years, many individual case reports elucidating unusual histologic features in neurofibroma have been added to the literature, some of which have defined ...
Neha S. Nagrani, Jag Bhawan
doaj   +1 more source

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