Results 61 to 70 of about 5,977 (216)

Neurofibromatosis type 1: Fundamental insights into cell signalling and cancer [PDF]

open access: yes, 2016
Neurofibromatosis type 1 (NF1) is an autosomal dominant tumour predisposition syndrome that is caused through loss of function mutations of a tumour suppressor gene called Neurofibromin 1.
Rad, Ellie, Tee, Andrew
core   +2 more sources

Lateral Cutaneous Branch of the Intercostal Nerve as a Donor Site for Nerve Reconstruction Following Enucleation of an Upper Extremity Schwannoma

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Fascicular defect after median nerve schwannoma enucleation reconstructed with a graft from the lateral cutaneous branch of the intercostal nerve. ABSTRACT The lateral cutaneous branch of the intercostal nerve is a reliable donor for upper extremity nerve reconstruction after schwannoma enucleation, offering easy anatomical access and potential for ...
Erika Koyama   +2 more
wiley   +1 more source

Bilateral Giant Plexiform Neurofibromas In Neurofibromatosis Type 1

open access: yesIndian Journal of Dermatology, 2002
A single plexiform neurofibroma or two of any type are considered diagnostic of neurofibromatosis type 1 (NF). Plexiform neurofibromas are congenital and pathognomonic for NF-1.
Thappa D . M   +2 more
doaj  

Large pelvic plexiform schwannoma presenting with a perineal bulge in a child: A case report

open access: yesHuman Pathology Reports, 2023
Plexiform schwannoma (PS) is a rare tumor that accounts for only 5 % of all schwannomas. Most cases are small, measuring less than 3 cm in diameter, and involve the skin and superficial tissue of the head, neck, or trunk.
Najla Ben Ghashir   +4 more
doaj   +1 more source

Emerging genotype-phenotype relationships in patients with large NF1 deletions. [PDF]

open access: yes, 2017
The most frequent recurring mutations in neurofibromatosis type 1 (NF1) are large deletions encompassing the NF1 gene and its flanking regions (NF1 microdeletions).
Cooper, David N   +2 more
core   +2 more sources

Rare Association Between Neurofibromatosis Type 1 and Adrenocortical Carcinoma

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Axial slice CT abdomen pelvis with portal venous contrast, revealing a well circumscribed 22 × 20 × 22 mm left adrenocortical adenocarcinoma (ACC) in a patient with neurofibromatosis type 1 (NF1). ABSTRACT Although rare, adrenocortical carcinoma (ACC) should be considered in individuals with neurofibromatosis type 1 (NF1) presenting with adrenal ...
Zachary Pluim   +6 more
wiley   +1 more source

Solitary neurofibroma in the male breast [PDF]

open access: yes, 2007
BACKGROUND: Neurofibroma of the male breast outside of neurofibromatosis is extremely rare with only one previous case having been reported. CASE PRESENTATION: A 48 year old male patient with a neurofibroma in the breast presenting with gynaecomastia is ...
Deva S Jeyaretna   +11 more
core   +3 more sources

Unraveling a Hidden Mass: A 10‐Year Mystery of Groin Swelling Reveals an Unexpected Diagnosis of Neurofibroma

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
Unravelling a Hidden Mass: Case of 70‐year‐old female presenting with 10‐year history of painless groin swelling. Intraoperative discovery revealed an unexpected neurofibroma. ABSTRACT This case presents the perplexing journey of a 70‐year‐old woman with a decade‐long history of painless, gradually enlarging left‐side groin swelling.
Alaa Tajeldeen Habeeb Abdallah   +6 more
wiley   +1 more source

Facial plexiform neurofibroma in a child with neurofibromatosis type I: A case report

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2007
Plexiform neurofibroma is a non-circumscribed, thick, and irregular benign tumor of the peripheral nerve sheath. It is a virtually pathognomonic and often disabling feature of neurofibromatosis type I.
Patil K, Mahima V, Shetty S, Lahari K
doaj  

Neurofibroma plexiforme en mucosa yugal: presentación de un caso clínico [PDF]

open access: yes, 2004
Presentamos un caso clínico de neurofibroma plexiforme localizado en región geniana, a nivel submucoso. Su interés radica en que, a pesar de ser el tumor de origen neurógeno más frecuente, es una entidad poco habitual y que rara vez se localiza a nivel ...
Fernández-Alba Luengo, Javier   +4 more
core   +1 more source

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