Results 101 to 110 of about 50,529 (255)
Embryonal Rhabdomyosarcoma of Upper Lid in 15-Year-Old Patient
Case Reports in Ophthalmological Medicine, 2014 Rhabdomyosarcoma is the most common childhood primary malignant tumor of orbit. Most of patients present between the ages of 7 and 8 years. Pure eyelid rhabdomyosarcoma is a very rare tumor with only a few reported cases in the literature. We introduce a
Mohammad Sharifi
doaj +1 more source
European Journal of Haematology, EarlyView.ABSTRACT Background and Aims Retroperitoneal Infantile Fibrosarcoma (RIFS) is a rare, locally aggressive pediatric soft tissue tumor. Its retroperitoneal location poses challenges due to proximity and potential invasion of critical structures such as the inferior vena cava (IVC).
Gaia Brunetti +8 more
wiley +1 more source
Histopathology, EarlyView.New concepts, innovations and some issues have emerged since the adoption a decade ago of WHO/ISUP grading for CCRCC and PRCC. Continued use of the WHO/ISUP grading for CCRCC and PRCC has been upheld by newer studies, and practice guidance for some of the grading issues, where data are available, is provided.
Gladell P. Paner +4 more
wiley +1 more source
Dermatomyositis Associated with Laryngeal Rhabdomyosarcoma: A Case Report
The Turkish Journal of Gastroenterology, 2013 Dermatomyositis is a systemic autoimmune inflammatory disorder which is characterized by cutaneous manifestations and associated with various types of malignancies.
Gökçe Saygı UYSAL +4 more
doaj
Journal of Paediatrics and Child Health, EarlyView.ABSTRACT Aim Kaposiform haemangioendothelioma is a rare vascular tumour. Management has evolved over the last two decades, with most cases receiving vincristine or sirolimus. We aim to describe our experience with managing this tumour, with a focus on the safety and efficacy of vincristine.
Bronwen Kirk +4 more
wiley +1 more source
Soft Tissue: Rhabdomyosarcoma [PDF]
, 1900 Embryonal Rhabdomyosarcoma in Gluteal Region Metastatic to Lung (2 ...
MUSC Department of Pathology and Laboratory Medicine
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Case Reports in Genetics, 2017 Costello syndrome is caused by heterozygous de novo missense mutations in the protooncogene HRAS with tumor predisposition, especially rhabdomyosarcoma. We here report two pediatric patients with Costello syndrome and umbilical ligament rhabdomyosarcoma.
Carlos Sánchez-Montenegro +7 more
doaj +1 more source
TANC1::HTRA1 fusion in schwannomas
Brain Pathology, EarlyView.
Ilay Caliskan +3 more
wiley +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 8, August 2026.ABSTRACT Background Osteosarcoma (OS) and Ewing sarcoma (EWS) are the most common primary bone cancers in children, but acute thrombosis is poorly characterized in this population. Our study evaluated the rates of venous thromboembolism (VTE) and associated risk factors in pediatric patients with bone sarcomas treated over a 10‐year period encompassing
Sarah Kappa +8 more
wiley +1 more source
Embryonal Rhabdomyosarcoma [PDF]
, 2001 A case of embryonal rhabdomyosarcoma of vagina in an infant is being reported here because of its rarity and the changing trend in the ...
Halder A +4 more
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