Results 91 to 100 of about 5,977 (216)

Acute median nerve palsy due to hemorrhaged schwannoma: case report [PDF]

, 2007
Schwannomas are common, benign nerve tumors originating from the sheath of peripheral nerves. In this article, a 54 year old woman suffered from sudden onset motor and sensory deficit at her first radial three fingers on her right hand.
Mehmet Aydin, Dilcan Kotan, Muzaffer Keles   +2 more
core   +2 more sources

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

Malignant peripheral nerve sheath tumour: A rare tumour of the breast [PDF]

, 2010
Malignant peripheral nerve sheath tumour is a rare tumour of the breast and this report highlights the radiological and histological features and the difficulties in making a diagnosis. A high index of suspicion when dealing with a breast lesion that has
Akhator, A, Inikori, A, Nwanchokor, FN, Oside, CP   +3 more
core  

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

Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine [PDF]

, 2015
Malignant peripheral nerve sheath tumors (MPNSTs) are soft-tissue sarcomas that can arise either sporadically or in association with neurofibromatosis type 1 (NF1).
Adriana López‐Doriga, Alberto Villanueva, August Vidal, Bernat Gel, Conxi Lázaro, Diana Pérez‐Sidelnikova, Eduard Serra, Ernest Terribas, Ferner RE, Gabriel Capellá, Guha A, Ignacio Blanco, Javier García‐del Muro, Joan Castellsagué, Joan Maria Viñals, Juana Fernández‐Rodríguez, Miguel Angel Pujana, Rafael Valdés‐Mas, Roger Llatjós, Turk AN, Xose S Puente, Yolanda Benavente   +21 more
core   +2 more sources

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  

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