Results 91 to 100 of about 31,395 (237)
Large pelvic plexiform schwannoma presenting with a perineal bulge in a child: A case report
Human 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
Neurofibromatosis 2011: a report of the Children’s Tumor Foundation Annual Meeting [PDF]
, 2011 The 2011 annual meeting of the Children\u27s Tumor Foundation, the annual gathering of the neurofibromatosis (NF) research and clinical communities, was attended by 330 participants who discussed integration of new signaling pathways into NF research ...
Alison C. Lloyd +21 more
core +3 more sources
Cancer Medicine, Volume 15, Issue 2, February 2026.Encouraging survival is achieved in phakomatosis syndromes with conventional multimodality treatment (Surgery, RT, chemotherapy). There is an urgent need for easily administered systemic therapies which improve both quality and quantity of life. ABSTRACT Purpose Phakomatoses‐associated primary central nervous system (CNS) tumors are therapeutically ...
Anuradha Krishnan +10 more
wiley +1 more source
Emerging genotype-phenotype relationships in patients with large NF1 deletions. [PDF]
, 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
Cancer, Volume 132, Issue 3, 1 February 2026.Abstract Background Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas with a 5‐year survival rate of approximately 50%, secondary to their metastatic potential and resistance to therapy. MPNSTs can arise sporadically, as a late toxicity from therapeutic radiotherapy, or in patients with neurofibromatosis type 1 (NF1).
Rachel E. Aubrey +7 more
wiley +1 more source
Facial plexiform neurofibroma in a child with neurofibromatosis type I: A case report
Journal 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
Solitary neurofibroma in the male breast [PDF]
, 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
European Journal of Neurology, Volume 33, Issue 2, February 2026.Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley +1 more source
BMC Surgery, 2020 Background A large plexiform neurofibroma in patients with neurofibromatosis type I can be life threatening due to possible massive bleeding within the lesion.
Taro Mikami +11 more
doaj +1 more source
Solitary intraosseous neurofibroma of the mandible. Apropos of a case [PDF]
, 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