Results 51 to 60 of about 8,039 (180)

UGT1A1 genotype testing for irinotecan: A guideline developed by the UK Centre of Excellence in Regulatory Science and Innovation in Pharmacogenomics (CERSI‐PGx)

British Journal of Clinical Pharmacology, EarlyView.
Abstract Irinotecan, a topoisomerase I inhibitor, is available as both non‐pegylated and pegylated formulations. The non‐pegylated formulation is licensed for use in advanced colorectal cancer either in combination with other agents or as monotherapy.
Dharmisha Chauhan, Cinzia Dello Russo, Jack Thompson, Dyfrig A. Hughes, Katherine Payne, Maria Tsakiroglou, Paul Ross, Rena Chauhan, Simon Jenkinson, Jessica Keen, Sophie Harding, Eleanor Lau, Michael Braun, Roshan Agarwal, Richard Adams, Elisabeth Rolf, Farah Al‐Sheikhli, Sarah Mitchell, Ruth Hammond, Rosie Roberts, Lorna Cairns, Shirley Heggarty, Janet Graham, Justin Mencel, Munir Pirmohamed   +24 more
wiley   +1 more source

Extraskeletal Ewing’s Sarcoma Arising from the Sciatic Nerve: A Diagnostic Challenge [PDF]

, 2015
Ewing’s sarcoma is a common bone tumour of childhood but is a rare occurrence in individuals over 20 years of age. Few cases are reported as originating from peripheral nerves.
Aadhar Sharma, John Skinner, Jeremy Whelan, Michael Fox, Kate Brown   +4 more
core   +1 more source

Primitive Neuroectodermal Tumor of the Cervix Uteri

International Journal of Hematology-Oncology and Stem Cell Research, 2012
Ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.It is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide.
Zineb Benbrahim, Christine Haie-Meder, Pierre Duvillard, Omar El Mesbahi, Axel Le Cesne, Patricia Pautier   +5 more
doaj  

Gene expression response to EWS–FLI1 in mouse embryonic cartilage

Genomics Data, 2014
Ewing's sarcoma is a rare bone tumor that affects children and adolescents. We have recently succeeded to induce Ewing's sarcoma-like small round cell tumor in mice by expression of EWS–ETS fusion genes in murine embryonic osteochondrogenic progenitors ...
Miwa Tanaka, Ken-ichi Aisaki, Satoshi Kitajima, Katsuhide Igarashi, Jun Kanno, Takuro Nakamura   +5 more
doaj   +1 more source

Extra-skeletal Ewing’s sarcoma of the leg with multiple skeletal and pulmonary metastases: A rare pediatric case report

SAGE Open Medical Case Reports, 2023
Being the second most common malignant bone tumor in children and young adults, Ewing’s sarcoma can also occur as a primary soft-tissue tumor called extraosseous or extra-skeletal Ewing’s sarcoma.
Yahya El Harras, Safaa Choayb, Khadija Laasri, Nazik Allali, Latifa Chat, Siham El Haddad   +5 more
doaj   +1 more source

Challenges and Pitfalls to Diagnosing NUTM1‐Rearranged Neoplasia of the Pancreas by Cytology and Ancillary Studies

Diagnostic Cytopathology, EarlyView.
ABSTRACT Fine‐needle aspiration cytology specimens are frequently utilized for ancillary studies to identify diagnostic and prognostic information. This case highlights diagnostic pitfalls and challenges in diagnosing NUTM1‐rearranged neoplasia on pancreatic cytology.
Terrance J. Lynn
wiley   +1 more source

Primary renal Ewing’s sarcoma in an adult: an enigma

, 2021
Extraskeletal Ewing’s sarcoma is a rarity, with a renal primary in an adult, being even rarer. There is no consensus on the optimal imaging modality, as well as best therapeutic option, making them an enigma for ...
Aggarwal Gaurav, Gupta Sujoy, Das Suvraraj, Midha Divya   +3 more
core   +1 more source

Primitive Neuroectodermal Tumor of the Cervix Uteri: A case report and review of literature

International Journal of Hematology-Oncology and Stem Cell Research, 2015
Ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.It is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide.
Zineb Benbrahim, Christine Haie-Meder, Pierre Duvillard, Omar El-Mesbahi, Axel Le-Cesne, Patricia Pautier   +5 more
doaj  

Primary Pulmonary Mesenchymal Neoplasm With EWSR1::CREM Fusion: Cytologic Findings and Molecular Diagnosis

Diagnostic Cytopathology, EarlyView.
ABSTRACT Background Primary pulmonary mesenchymal neoplasms with EWSR1::CREM fusion are rare. These lesions are challenging to diagnose by morphology and immunohistochemistry alone. Case A 66‐year‐old woman (ex‐smoker) was found to have a 1.3‐cm right lower lobe lung nodule that had grown very slowly over a 9‐year period.
Priya Upadhyay, Sanjay Mukhopadhyay, Swikrity U. Baskota   +2 more
wiley   +1 more source

Ewing’s sarcoma / Primitive Neuroectodermal tumor of uterine cervix: a rare case report

, 2016
Ewing’s sarcoma, a round cell malignancy of bone and soft tissue occurs predominantly in adolescents and young adults. Extraosseous Ewing’s sarcoma is extremely rare.
R. Tanwar, N. Rastogi, P. Mandawat, N. Soni, A. Gupta, R.K. Singh   +5 more
core   +1 more source