Results 121 to 130 of about 31,395 (237)

Plexiform Neurofibroma of the Submandibular Salivary Gland in a Child

Canadian Journal of Gastroenterology, 2001
Plexiform neurofibromas in major salivary glands are rarely described. In the literature, most reported tumours have been present in the parotid gland region.
Jacqueline M Bourgeois, Jasim Radhi, Lisa Elden, Gerald Gill   +3 more
doaj   +1 more source

Morphological spectrum of peripheral nerve sheath tumors: A series of 126 cases

Indian Journal of Pathology and Microbiology, 2009
By convention, soft tissue tumors include the peripheral nerve sheath tumor (PNST) although they arise from neuroectoderm. PNSTs display a wide spectrum of morphology and biological behavior.
Gabhane Sushma, Kotwal Mrunamayi, Bobhate Sudhakar   +2 more
doaj  

Multidisciplinary Management of a Giant Plexiform Neurofibroma by Double Sequential Preoperative Embolization and Surgical Resection

Case Reports in Neurological Medicine, 2013
Plexiform neurofibromas are benign tumors originating from subcutaneous or visceral peripheral nerves, which are usually associated with neurofibromatosis type 1.
Roberto Vélez, Sergi Barrera-Ochoa, David Barastegui, Mercedes Pérez-Lafuente, Cleofe Romagosa, Manuel Pérez   +5 more
doaj   +1 more source

Diffuse plexiform neurofibroma [PDF]

Indian Journal of Surgery, 2010
S Sujith, Kumar, D Muthiah Selva, Kumar, R, Thirunavukuarasu   +2 more
openaire   +2 more sources

Giant Plexiform Neurofibroma

Journal of Surgical Dermatology, 2020
We report a rare case of giant plexiform neurofibroma in a patient affected by type-1 neurofibromatosis and we describe the correct surgical management of such lesions in order to avoid intra- and post-op blood loss related complications.
Michelangelo Giovanni Vestita, Rossella Elia, Giuseppe Giudice   +2 more
openaire   +3 more sources

Pelvic neurofibroma arising from prostate in a case of neurofibromatosis-1

Indian Journal of Urology, 2011
Pelvic neurofibroma is a rare condition and can be associated with neurofibromatosis-1 (NF-1). The diagnosis is primarily based on histopathology, though certain characteristic imaging features like the ′target sign′ on T2W MRI are highly suggestive of ...
Manisha Jana, Shivanand Gamanagatti, Rajeev Kumar, Sandeep Aggarwala   +3 more
doaj   +1 more source

Syndrome in question [PDF]

, 2016
Neurofibromatosis is extremely variable in its presentation. Segmental neurofibromatosis (SNF), which corresponds to NF-type 5 in the Riccardi classification, is a rare disorder. It may go unrecognized if few lesions are observed.
Carvalho, S., Horta, M., Oujo, E., Rosmaninho, A.   +3 more
core   +3 more sources

Unilateral Creeping Destruction of Deformed Mandibular Ramus and Angle Associated with Extensive Facial Plexiform Neurofibroma in Neurofibromatosis Type 1: A Case Report with Analysis of the Literature for Diagnosing Osteolytic Events of the Mandible in Tumor-suppressor Gene Syndrome

Anticancer Research, 2018
Neurofibromatosis type (NF1) is an autosomal dominant inherited tumor-suppressor gene syndrome of significant phenotypic variability with probable complete penetrance of the disease. Skeletal malformations of the skull belong to the phenotype of NF1.
R. Friedrich, H. Scheuer
semanticscholar   +1 more source

Facial transplantation: a concise update [PDF]

, 2013
Objectives: Update on clinical results obtained by the first worldwide facial transplantation teams as well as review of the literature concerning the main surgical, immunological, ethical, and follow-up aspects described on facial transplanted patients.
Barrera Pulido, Fernando, Gacto Sánchez, Purificación, García-Perla García, Alberto, González Padilla, J.D., Gómez Cia, Tomás, Hernández Guisado, J. M., Infante Cossío, Pedro, Lagares Borrego, Araceli, Narros Giménez, Rocío, Sicilia Castro, D.   +9 more
core   +1 more source

A case of large diffuse cutaneous neurofibroma masquerading as plexiform variant: Diagnostic challenges [PDF]

Journal of Krishna Institute of Medical Sciences University
Diffuse Cutaneous Neurofibroma (DCN) is an infrequently encountered clinical entity that can be challenging to diagnose due to its variable clinical presentation, radiological findings, and histopathological features.
Shivani S Rao , Ranjana S Ranade
doaj