Results 121 to 130 of about 54,150 (267)
Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Persistent unilateral otalgia, especially when refractory to treatment and associated with cranial nerve signs, should prompt early imaging and nasopharyngeal evaluation to avoid delayed diagnosis of aggressive malignancies such as Burkitt lymphoma.
Sultaneh Haddad +9 more
wiley +1 more source
Rhabdomyosarcoma of the maxillary gingiva
, 2018 Rhabdomyosarcoma is a malignant skeletal muscle neoplasm. The tumor is much more common in children, and the most frequent site is head and neck region.
Samira Derakhshan +3 more
core +1 more source
Cytoskeletal Dynamics in Cancer: From Pathogenesis to Treatment
MedComm, Volume 7, Issue 10, October 2026.This review systematically addresses the fundamental roles of the cytoskeleton (actin filaments, microtubules, and intermediate filaments) in cancer progression. We focus on how cytoskeletal dynamics regulate tumor proliferation, metastasis, and programmed cell death, while also modulating the immune microenvironment. Understanding these mechanisms may
Jie Chen +9 more
wiley +1 more source
Current chemotherapeutic strategies for rhabdomyosarcoma.
, 2005 Rhabdomyosarcoma is a typical tumor of childhood and adolescence. Over the years there has been a gradual but important improvement in survival for patients with this tumor, despite its high grade of malignancy. These results are due to multidisciplinary
Ferrari A, Casanova M.
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The extract of Nicotiana glauca induces apoptosis in rhabdomyosarcoma cells
Rhabdomyosarcoma, a malignant tumor commonly found in children and adolescents, often carriesa poor prognosis. We conducted studies on the effects of the liposoluble extract of Nicotiana glauca (N.
Pronsato, Lucía +4 more
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Superficial Ewing Sarcoma of the Rectum: A Case Report and the Utility of Molecular Diagnostics
Journal of Cutaneous Pathology, Volume 53, Issue 10, Page 917-920, October 2026.ABSTRACT Ewing sarcoma is an undifferentiated small round cell sarcoma that most commonly presents as a malignant bone tumor in pediatric and young adult patients. The diagnosis is typically confirmed by molecular genetic identification of a fusion protein, most commonly involving members of the FET and ETS gene families.
Jessica L. Muldoon +3 more
wiley +1 more source
Histopathology, Volume 89, Issue 4, Page 574-589, October 2026.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
Rhabdomyosarcoma of the prostate [PDF]
, 1986 We report a case of rhabdomyosarcoma of the prostate. The patient was a 56-year-old man who complained of anal pain and dysuria. Tumor of the prostate was suspected after rectal examination.
村瀬, 達良 +5 more
core
A 3‐year‐old girl with a left optic nerve tumor
Brain Pathology, EarlyView.
Samuel López Muñoz +10 more
wiley +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 9, September 2026.ABSTRACT Pediatric radiation therapy presents unique challenges compared to adult treatments, including those of immobilization, potential need for sedation, and the critical importance of accurate, reproducible positioning. Additionally, heightened attention to imaging doses is necessary to minimize long‐term toxicity in survivors.
Parham Alaei +17 more
wiley +1 more source