Results 71 to 80 of about 7,740 (174)

Combined Neurolysis of the Gasserian and Sphenopalatine Ganglia in Children with Sinonasal Alveolar Rhabdomyosarcoma: Innovative Strategies for Pediatric Oncological Pain Management

open access: yesIndian Journal of Pain
Rhabdomyosarcoma is an uncommon tumor but is the most frequent soft-tissue sarcoma in children. It is classified into four histological subtypes: embryonal, alveolar, pleomorphic, and spindle cell.
Bilena Margarita Molina Arteta   +2 more
doaj   +1 more source

A bright future for multidisciplinary approach to cancer care in the setting of limited resource

open access: yesTranslational Oncology
We report a case of alveolar rhabdomyosarcoma of the infratemporal region in a female child. An 8year old female was diagnosed with alveolar rhabdomyosarcoma 10 years ago.
Mary-Ann Dadzie   +3 more
doaj   +1 more source

An extremely rare case of testicular malign neoplasm; alveolar subtype of rhabdomyosarcoma with long term follow-up.

open access: yesJournal of Health Sciences, 2014
Testicular neoplasm usually occur in men aged between 15 and 35. These are solid organ tumours and also should be operated when there is a suspicious clinical findings. Testis tumours are levelled after histopathology evaluation.
Tumay Ipekci   +3 more
doaj   +1 more source

Primary Gastric Alveolar Rhabdomyosarcoma

open access: yesInternal Medicine
Primary gastric alveolar rhabdomyosarcoma (RMS) is an extremely rare condition. We report a case of a 32-year-old man who presented with abdominal distension and anorexia. Imaging revealed a gastric mass with peritoneal dissemination and vertebral metastasis. Endoscopy revealed a large, ulcerative lesion. Histopathology revealed small round cells in an
Sakata, Yuhei   +9 more
openaire   +2 more sources

Pleomorphic rhabdomyosarcoma in adults: a case report

open access: yesJournal of Medical Case Reports
Background Rhabdomyosarcoma is a rare type of soft-tissue sarcoma that is more frequently observed in children and is less common in adults. Rhabdomyosarcoma can occur in any part of the body, including tissues without skeletal muscles. The main subtypes
Zahra Aminparast   +2 more
doaj   +1 more source

Alveolar Rhabdomyosarcoma of the Nasal Dorsum of a Pediatric Patient: A Case Report

open access: yesEar, Nose & Throat Journal
Alveolar rhabdomyosarcoma is a rare pediatric malignant tumor with a poor prognosis, and it is exceedingly rare for this tumor to manifest on the skin of the nasal dorsum. Therefore, timely and accurate treatment can improve the survival rate of patients.
Jingyu Chen BS   +4 more
doaj   +1 more source

Entinostat as a combinatorial therapeutic for rhabdomyosarcoma

open access: yesScientific Reports
Rhabdomyosarcoma (RMS) is the most common childhood soft tissue sarcoma. For the alveolar subtype (ARMS), the presence of the PAX3::FOXO1 fusion gene and/or metastases are strong predictors of poor outcome. Metastatic PAX3::FOXO1 + ARMS often responds to
Shefali Chauhan   +11 more
doaj   +1 more source

Silent Killer in the Nose: Two Cases of Nasal Alveolar Rhabdomyosarcoma in Adults. [PDF]

open access: yesCureus, 2023
Ahmad Fahmi AK   +4 more
europepmc   +1 more source

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