Results 51 to 60 of about 5,407 (151)

Safety and Efficacy of Nephron‐Sparing Surgery in Bilateral Wilms Tumors: A Systematic Review and Meta‐Analysis

Health Science Reports, Volume 9, Issue 1, January 2026.
ABSTRACT Background and Aims Bilateral Wilms tumor (BWT) presents a significant challenge in pediatric oncology, necessitating a delicate balance between achieving oncological control and preserving renal function. While nephron‐sparing surgery (NSS) has emerged as a promising alternative to radical nephrectomy, its overall safety and efficacy profile ...
Menna Sarhan, Yasmine Adel Mohammed, Ayah Abdulgadir, Ibrahim Moqbel, Yehia Nabil Abdalla, Salma Allam, Ahmad Alkheder, Khaled Alsayed Abualkhair   +7 more
wiley   +1 more source

Alternative Chemotherapy Schedules in Ewing's Sarcoma: An Indian Perspective

Asian Journal of Oncology, 2018
Advances in the treatment of Ewing's sarcoma family of tumors (ESFTs) are a result of improvements in systemic and local therapies. VACA (vincristine, Adriamycin [doxorubicin], cyclophosphamide, dactinomycin) chemotherapy alone versus VACA + IE (VACA ...
Pramod Kumar Singh, Rakesh Kapoor, Ravi Teja, Ritesh Kumar, Amit Bahl   +4 more
doaj   +1 more source

Results of novel strategies for treatment of Wilms' tumor

International Brazilian Journal of Urology, 2007
OBJECTIVE: To evaluate treatment outcomes in Wilms' tumor (WT). MATERIALS AND METHODS: We studied 53 children with median age of 2 years with WT, stages I-19, II-14, III-12, IV-6 and V-2.
Silvio Tucci Jr, Adauto J. Cologna, Haylton J. Suaid, Elvis T. Valera, Luis F. Tirapelli, Edson L. Paschoalin, Antonio C. Martins   +6 more
doaj   +1 more source

Synchronous Ectopic Adrenal Rhabdomyosarcoma and Ipsilateral Cystic Nephroma Revealing a Diagnosis of DICER1‐Related Tumor Predisposition: A Case Report

Case Reports in Surgery, Volume 2026, Issue 1, 2026.
DICER1‐related tumor predisposition (DRTP) results from loss‐of‐function germline variants that predispose patients to numerous benign and malignant tumors. Cystic nephromas are among the most common neoplasms in patients with DRTP; however, there are no reports of rhabdomyosarcoma from adrenal tissue in children with DRTP.
Alejandro O. Chara, Vikas S. Gupta, Jiancong Liang, Scott C. Borinstein, Daniel J. Benedetti, Julia Shelton, Semonti Nandi   +6 more
wiley   +1 more source

Whole abdominopelvic intensity-modulated radiation therapy for peritoneal disseminated rhabdomyosarcoma with three-year follow-up: a case report

Radiation Oncology, 2019
Background The role of local radiotherapy in the treatment of metastatic rhabdomyosarcoma is important. However, with peritoneal dissemination, the application of local therapy is challenging. Although there are few reports addressing the efficacy of the
Mariko Kawamura, Kuniyasu Okudaira, Yoshiyuki Itoh, Takeshi Kamomae, Eri Nishikawa, Hideki Muramatsu, Yoshiyuki Takahashi, Kazuki Yokota, Shinji Naganawa   +8 more
doaj   +1 more source

Resection of a Deep Pubic Alveolar Rhabdomyosarcoma With an Inferior Pubic Ramus Osteotomy Through a Perineal Approach: A Case Report

Case Reports in Orthopedics, Volume 2026, Issue 1, 2026.
Case A 17‐year‐old male who presented with urinary retention was found to have an alveolar rhabdomyosarcoma involving the peritoneum, prostate, and bladder. After neoadjuvant chemotherapy, a residual mass in the obturator internus muscle was resected through a perineal approach and inferior pubic ramus osteotomy.
Brian Kwan, Dylan Shafer, Bonnie Balzer, Leo Mascarenhas, Daniel C. Allison, Shashank Kaushik   +5 more
wiley   +1 more source

A Case of Ewing’s Sarcoma of the Mediastinum in a 63‐Year‐Old Woman Initially Misdiagnosed as Non‐Small‐Cell Lung Cancer Successfully Treated With Chemotherapy and Radiation With a Durable Response

Case Reports in Oncological Medicine, Volume 2026, Issue 1, 2026.
Mediastinal Ewing’s sarcoma is an exceptionally rare malignancy, with an incidence of approximately 0.3%. Due to the rarity of the tumor and challenges such as limited tissue availability, diagnosis can be difficult. Curative treatment typically requires a multimodal approach, including intensive chemotherapy, surgery, and radiation therapy.
Anusha Manje Gowda, Navkirat Kahlon, Nagaraju Mupparapu   +2 more
wiley   +1 more source

Inflammation of actinic keratoses after the use of docetaxel plus cyclophosphamide

Current Problems in Cancer: Case Reports
Actinic keratoses are common pre-malignant lesions of the skin that have been documented to become inflamed after the use of chemotherapy. Several agents, such as 5-fluorouracil, capecitabine, pentostatin, dactinomycin, vincristine, dacarbazine ...
Ashley Wittmer, Lindsey Finklea, Jonathan Joseph   +2 more
doaj   +1 more source

Multiomics Integration and Pharmacovigilance Mining to Decode the Molecular Mechanisms and Biomarkers of Drug‐Induced Hepatic Sinusoidal Obstruction Syndrome

International Journal of Clinical Practice, Volume 2026, Issue 1, 2026.
Purpose This study aimed to systematically identify drug‐associated signals for hepatic veno‐occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) using large‐scale real‐world data and to decode the underlying molecular mechanisms of high‐risk agents.
Yafei He, Tianyu She, Wenhua Lin, Shanshan Cai, Hongliang Cong, Zhiwen Luo   +5 more
wiley   +1 more source

Tuberous Sclerosis Associated with Biphasic Adult Wilms' Tumor: A Case Report and Review of Literature

Indian Journal of Medical and Paediatric Oncology
Tuberous sclerosis is an autosomal dominant genetic disorder characterized by lesions in the skin and benign tumors in various organs—retina, lungs, heart, brain, skin, and kidneys. Wilms' tumor is rare in adults. We present a unique case of Wilms' tumor
Amit R. Sharma, R. T. Raghavendra, Pradhuman Yadav   +2 more
doaj   +1 more source