Clinical course in children and adolescents with neurofibromatosis type 1: clinical features in correlation with age of manifestation and molecular genetics [PDF]
, 2023 Background: Neurofibromatosis type I (NF1) is the most frequent tumour-disposing genetic disorder and occurs worldwide with an incidence of about 1:3000 births (1).
Ryczek, Monika
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S1‐Leitlinie kutane Angiosarkome – Update 2021
, 2021 JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 19, Issue 12, Page 1801-1813, December 2021.
Thomas Vogt +11 more
wiley +1 more source
Schwannoma of the tongue in a child [PDF]
, 2010 A schwannoma or neurilemmoma is a benign, slow growing, usually solitary and encapsulated tumour originating from Schwann cells of the nerve sheath.
Lukšić, Ivica +4 more
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Mandibular trigeminal schwannoma: case report [PDF]
, 2001 We report one case of peripheral trigeminal schwannoma originated from the mandibular branch (V3) and located inside the infratemporal and pterygopalatine fossae with slight intracranial extension.
Braga, Fernando de Menezes +2 more
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Neurofibrome de l’avant bras: à propos d’un cas [PDF]
, 2016 Les tumeurs des nerfs périphériques sont rares et mal connues. Le diagnostic en est rarement fait avant l'intervention. Le traitement chirurgical est difficile, et risque d'entrainer des dégâts nerveux irréversibles s'il est mal conduit. Nous rapportons
Fahim, Hda, Hasnaoui, Khadija
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An Isolated Neurofibromal Polyp of the Colon [PDF]
Case Reports in Gastroenterology, 2012 Solitary neurofibromal colonic polyps are a rare entity, particularly outside the setting of neurofibromatosis type 1. The clinical significance of such lesions has not yet been established. Though typically benign tumors, neurofibromas have been reported to undergo malignant transformation, with an increased risk of malignancy when associated with ...
Pierre Hindy +5 more
openaire +3 more sources
Tumeur maligne des gaines nerveuses périphériques révélant une neurofibromatose type 1 [PDF]
, 2010 La Neurofibromatose type 1 (NF1) ou maladie de Von Recklinghausen est une affection à expression clinique variable. La transformation maligne est rare et redoutable.
Boudawara, T +10 more
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Pertinence du neuromonitoring multimodal dans les lesions doubles : A propos de la prise en charge, a l’hopital neurologique de lyon, d’une scoliose congenitale avec deficit neurologique rapide [PDF]
, 2021 Nous rapportons un cas illustrant qu’une évaluation clinique, radiologique et neurophysiologique exhaustive est obligatoire avant une chirurgie de scoliose sévère.
Andre-Obadia, Nathalie +5 more
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Chondroblastome para vertébrale et iliaque : une observation rare: Para vertebral and iliac chondroblastoma: a rare case report [PDF]
, 2021 Chondroblastoma, a rare benign cartilage tumor, most often found in long bones, rarely in flat bones. The authors report a case of para vertebral and right iliac chondroblastoma in a 31-year-old patient with tumefaction in the right lumbar fossa ...
Esika, Jean Paul +4 more
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