نتایج جستجو برای: schwannomas

تعداد نتایج: 1871  

Journal: :International journal of oncology 2009
Victor Martinez-Glez Carmen Franco-Hernandez Luis Alvarez Jose M De Campos Alberto Isla Jesus Vaquero Luis Lassaletta Cacilda Casartelli Juan A Rey

Microarray gene expression profiling is a high-throughput system used to identify differentially expressed genes and regulation patterns, and to discover new tumor markers. As the molecular pathogenesis of meningiomas and schwannomas, characterized by NF2 gene alterations, remains unclear and suitable molecular targets need to be identified, we used low density cDNA microarrays to establish exp...

Journal: :World Journal of Surgical Oncology 2008
Theodosios Theodosopoulos Vaia K Stafyla Paraskevi Tsiantoula Anneza Yiallourou Athanasios Marinis Agathi Kondi-Pafitis Achilleas Chatziioannou Efstathios Boviatsis Dionysios Voros

BACKGROUND Retroperitoneal schwannomas are rare, usually benign tumors that originate in the neural sheath and account for only a small percentage of retroperitoneal tumors. The aim of this clinical study is to present our experience in managing retroperitoneal schwannomas with a review of the current literature and to point out the surgical technical difficulties we faced, due to the tumor's s...

Journal: :Ortopedia, traumatologia, rehabilitacja 2016
Ranjit Kumar Baruah Suresh Bora Russel Haque

UNLABELLED To report a case of segmental schwannomatosis involving the dorsal and lumbar spine and describe its excision as well as review of literature on schwannomatosis involving the spine. SUMMARY OF BACKGROUND DATA Schwannomas are nerve sheath tumours which usually occur as solitary lesions. Presence of multiple schwannomas suggests a genetic predisposition to tumorogenesis and possible ...

Journal: :Journal of clinical and diagnostic research : JCDR 2013
A L Hemalatha Vani D Giripunja M Bharathi M Geetanjali S

Schwannomas otherwise referred to as neurilemmomas are benign, slowly progressing, encapsulated tumors arising from Schwann cells in the peripheral nerve sheath. They may grow along any peripheral or cranial nerve. Amongst the cranial nerve schwannomas, the eigth cranial nerve is the commonest site. But orbit is a rare site for their occurrence. Solitary orbital schwannomas account for 1% of or...

Journal: :AJNR. American journal of neuroradiology 1991
J Abramowitz J E Dion M E Jensen M Lones G R Duckwiler F Viñuela J R Bentson

Schwannomas are tumors derived from nerve sheath cells, which are often located in the head and neck, including the CNS. Although a definitive vascular pattern has been previously characterized for these lesions, preoperative embolization of the more vascular schwannomas has not been described. In a review of eight patients with schwannomas who underwent angiography at our institution since 198...

2017
Erdal Uysal Göktürk Maralcan Türkay Kırdak Hasan Bakır Mehmet Sökücü Reşat Kervancıoğlu

Schwannomas are tumors originating from Schwann cells in the nerve sheath. Although they can appear on many parts of the body, they occur most frequently in the head and neck. Furthermore, they are very rarely seen in the retroperitoneal region. Ancient schwannoma is a sub-type of schwannomas that is quite rare. In this study, the case of a retroperitoneal ancient schwannoma, which showed cysti...

2013
MIGUEL TORRES-MARTIN LUIS LASSALETTA JESUS SAN-ROMAN-MONTERO JOSE M. DE CAMPOS ALBERTO ISLA JAVIER GAVILAN BARBARA MELENDEZ GIOVANNY R. PINTO ROMMEL R. BURBANO JAVIER S. CASTRESANA JUAN A. REY

Vestibular schwannomas are benign neoplasms that arise from the vestibular nerve. The hallmark of these tumors is the biallelic inactivation of neurofibromin 2 (NF2). Transcriptomic alterations, such as the neuregulin 1 (Nrg1)/ErbB2 pathway, have been described in schwannomas. In this study, we performed a whole transcriptome analysis in 31 vestibular schwannomas and 9 control nerves in the Aff...

Journal: :Neuro-oncology 2014
Alizée Boin Anne Couvelard Christophe Couderc Isabel Brito Dan Filipescu Michel Kalamarides Pierre Bedossa Leanne De Koning Carine Danelsky Thierry Dubois Philippe Hupé Daniel Louvard Dominique Lallemand

BACKGROUND Inactivation of the NF2 gene predisposes to neurofibromatosis type II and the development of schwannomas. In vitro studies have shown that loss of NF2 leads to the induction of mitogenic signaling mediated by receptor tyrosine kinases (RTKs), MAP kinase, AKT, or Hippo pathways. The goal of our study was to evaluate the expression and activity of these signaling pathways in human schw...

Journal: :Journal of neuropathology and experimental neurology 2005
Christian Mawrin Stefan Schulz Anja Hellwig-Patyk Elmar Kirches Albert Roessner Uwe Lendeckel Raimund Firsching Christian K Vorwerk Gerburg Keilhoff Knut Dietzmann Kirsten Grimm Guy Lindberg David H Gutmann Bernd W Scheithauer Arie Perry

Although somatostatin receptors have been detected in many normal and neoplastic tissues, little is known of their expression and function in peripheral nerve tumors. In the present study, we examined the expression of all 5 somatostatin receptor subtypes (sst1-5) in 3 normal peripheral nerves, 3 traumatic neuromas, 27 schwannomas, 18 neurofibromas, and 177 malignant peripheral nerve sheath tum...

2004
Samson W. Fine Steve A. McClain Maomi Li

We studied 25 cases of schwannoma and 42 cases of neurofibroma immunohistochemically with antibodies to calretinin and S-100 protein to explore the potential usefulness of calretinin in differentiating schwannomas from neurofibromas. Of 25 schwannomas, 24 (96%) showed moderate to strong staining for calretinin, with the extent of staining ranging from focal to diffuse. In contrast, only 3 (7%) ...

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