Results 1 to 10 of about 78,942 (313)

YAP1::MAML2 fusion, a newly identified genetic anomaly in a posterior fossa infant tumor, associated with the methylation class “embryonal tumor with multilayered rosettes, non-C19MC-altered” in the Heidelberg central nervous system tumor classifier and “embryonal tumor with multilayered rosettes-DICER” in the NIH classifier [PDF]

Acta Neuropathologica Communications
Embryonal tumors with multilayered rosettes (ETMR) are rare embryonal tumors that usually affect children under two years old. They are characterized histologically by the presence of multilayered rosettes and by the immunohistochemical expression of ...
Catherine Godfraind, Nabil Djebbour, Romain Appay, Anne Pagnier, Raia Doumit, Julien Masliah-Planchon, Fabien Forest, Fanny Burel-Vandenbos, Jean Boutonnat, Berengere Dadone-Montaudié   +9 more
doaj   +2 more sources

Mutant CTNNB1 and histological heterogeneity define metabolic subtypes of hepatoblastoma [PDF]

EMBO Molecular Medicine, 2017
Hepatoblastoma is the most common malignant pediatric liver cancer. Histological evaluation of tumor biopsies is used to distinguish among the different subtypes of hepatoblastoma, with fetal and embryonal representing the two main epithelial components.
Stefania Crippa, Pierre‐Benoit Ancey, Jessica Vazquez, Paolo Angelino, Anne‐Laure Rougemont, Catherine Guettier, Vincent Zoete, Mauro Delorenzi, Olivier Michielin, Etienne Meylan   +9 more
doaj   +4 more sources

A rare case of pure-type embryonal carcinoma in a 75-year-old woman mimicking epithelial ovarian carcinoma [PDF]

Kosin Medical Journal, 2022
Embryonal carcinoma, a very rare ovarian germ cell tumor, involves pure and mixed phenotypes. Pure-type embryonal carcinoma has never been reported in postmenopausal women. The current case was, thus, misdiagnosed as an epithelial ovarian carcinoma based
Hyun Been Jo, Eun Taeg Kim, Nam Kyung Lee, Kyung Un Choi, Eon Jin Kim, Yun Joo Shin, Ki Hyung Kim, Dong Soo Suh   +7 more
doaj   +1 more source

Clinical Characteristics and Treatment Outcome of Pediatric Rhabdomyosarcoma; Retrospective Review

Journal of Cancer and Allied Specialties, 2021
Introduction: Rhabdomyosarcoma is the most common soft tissue sarcoma in children. This paper aimed to assess the stage, site, and treatment outcome among rhabdomyosarcoma (RMS) patients.
Zunaira Shaukat, Raheela Mansoor, Najma Shaheen, Saliha Sarfraz, Komal Seher   +4 more
doaj   +1 more source

Embryonal Rhabdomyosarcoma of Prostate in Adult: A Rare Case Report

Folia Medica Indonesiana, 2021
Rhabdomyosarcoma is the fifth most common type of soft tissue solid tumor in children and the most common in the last two decades. Rhabdomyosarcoma of the urogenital organ is a rare mesenchymal tumor, covering 22% of all Rhabdomyosarcoma cases.
Dimas Panca Andhika, Sunaryo Hardjowijoto   +1 more
doaj   +1 more source

Case Report: Pediatric Hepatic Rhabdomyosarcoma With Maximum Lifetime

Frontiers in Medicine, 2022
Primary intrahepatic rhabdomyosarcoma is an extremely rare malignant tumor. Here, we describe a case of embryonal rhabdomyosarcoma of the liver in a 7-year-old boy without any symptoms.
Xu Li, Xiang Li, Dian-Fei Yang, Miao Li, Hong-Qin Xu, Shuang Zheng, Pu-Jun Gao   +6 more
doaj   +1 more source

Hepatoblastoma in an 18- Year Old Female; Rare Entity

Nepalese Medical Journal, 2020
Hepatoblastoma is a rare malignant hepatic tumor in adults. It is associated with poor prognosis as it is usually diagnosed late when the tumor is completely unresectable.
Daisy Maharjan, Deepshikha Gaire, Ram Chandra Adhikari   +2 more
doaj   +1 more source

Paratesticular Rhabdomyosarcoma in Young Adult- A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2015
Para testicular rhabdomyosarcoma is a rare malignant tumour, which usually presents as a painless mass in the scrotum or groin. A case of para testicular rhabdomyosarcoma in a 17-year-old male is being reported here who presented with chronic scrotal ...
NAVIN KUMAR SINHA
doaj   +1 more source

Survival of Testicular Pure Embryonal Carcinoma vs. Mixed Germ Cell Tumor Patients across All Stages

Medicina, 2023
Background and Objectives: The impact of pure histological subtypes in testicular non-seminoma germ cell tumors on survival, specifically regarding pure embryonal carcinoma, is not well established.
Cristina Cano Garcia, Andrea Panunzio, Stefano Tappero, Mattia Luca Piccinelli, Francesco Barletta, Reha-Baris Incesu, Kyle W. Law, Lukas Scheipner, Zhe Tian, Fred Saad, Shahrokh F. Shariat, Derya Tilki, Alberto Briganti, Ottavio De Cobelli, Carlo Terrone, Alessandro Antonelli, Severine Banek, Luis A. Kluth, Felix K. H. Chun, Pierre I. Karakiewicz   +19 more
doaj   +1 more source

Embryonal Rhabdomyosarcoma of the Biliary Tree as a Differential in a Paediatric Patient Presenting with Biliary Dilatation: Not Always a Choledochal Cyst

Acta Medica Lituanica, 2022
Rhabdomyosarcoma is a soft tissue malignant musculoskeletal tumour and is the most prevalent soft-tissue sarcoma in the paediatric population. Although, Embryonal RMS of the biliary tree is a rare entity, however, it is the most common cause of ...
Tara Prasad Tripathy, Yashwant Patidar, Karamvir Chandel, Annapoorani Varadarajan, Vikrant Sood, Shalini Thapar Laroia   +5 more
doaj   +1 more source