Results 91 to 100 of about 12,658 (224)

Embryonal Rhabdomyosarcoma in the Pelvis of a 22-Year-Old Female: A Case Report

Marshall Journal of Medicine, 2022
Embryonal rhabdomyosarcoma is a rare soft-tissue sarcoma that is responsible for less than 1% of malignancies in the adult population. We present a case of a 22-year-old female with a six-month history of abnormal uterine bleeding that was found to have ...
Amber Wright, Jared Justice, Niru Nahar, Nadim Bou Zgheib   +3 more
doaj   +1 more source

Imaging insights suggesting a sinister cause of a breast mass in adolescents: A case of rhabdomyosarcoma in a teenager

European Journal of Case Reports in Internal Medicine
Background: Sarcomas of the breast are exceedingly rare, accounting for less than 1% of malignant breast tumors, with primary rhabdomyosarcomas being even rarer.
Mariam Malik, Rana Bilal Idrees, Maham Khalid, Ameema Munir, Saba Nawaz, Zainab Nawaz, Muhammad Hamid Chaudhary   +6 more
doaj   +1 more source

Giant intrascrotal embryonal rhabdomyosarcoma in an adult: a case report and review of the literature

Journal of Medical Case Reports, 2018
Background Intrascrotal embryonal rhabdomyosarcoma in adults is a rare tumor with high aggression and a poor prognosis. We report our patient’s case and review the relevant literature to improve the understanding of this rare disease. Case presentation A
Wentao Gong, Qingqiang Gao, Zhipeng Xu, Yutian Dai   +3 more
doaj   +1 more source

Embryonal rhabdomyosarcoma of orbit-A case report

Indian Journal of Ophthalmology, 1990
Embryonal rhabdomyosarcoma of orbit presenting as a case of rapid proptosis of the right eye is reported in a 4 year old male child. There was no evidence of recurrence during a follow up of 6 months.
Maurya OPS, Patel R, Thakur V, Singh Rajendra, Kumar Mohan   +4 more
doaj  

Congenital Embryonal Rhabdomyosarcoma of the Extraperitoneal Pelvic Space with a Prenatal Onset: A Case Report

대한영상의학회지, 2019
Rhabdomyosarcoma is the most common pediatric soft tissue malignancy, however, extraperitoneal origin of the tumor is rare and prenatal onset of the tumor is even more rare.
Seung-Jin Yoo, Bo-Kyeong Kang, Mimi Kim, Soon-Young Song, Byung-Hee Koh   +4 more
doaj   +1 more source

An Adult Case of Paratesticular Spindle Cell Rhabdomyosarcoma

Urology Case Reports, 2014
Paratesticular rhabdomyosarcoma (RMS) occurs more frequently in children and is rare in adults. Embryonal RMS is the most common subtype of paratesticular RMS.
Joan C. Delto, George F. Wayne, Sofia Garces, Ana M. Medina, Alan M. Nieder   +4 more
doaj   +1 more source

Rhabdomyosarcoma embryonal type: in a three and a half year old girl [PDF]

, 2008
Rhadomyosarcoma is the most common tumour of the soft tissues in infants and children. We report a case of a 3 1/2 year old girl who presented with a swelling over the neck. Swelling was diagnosed as Rhabdomyosarcoma (embryonal type).
Fatimi, Saulat H., Gowani, Saqib Ali, Khan, Asmatullah, Khowaja, Ameer A   +3 more
core   +1 more source

Characterisation of Wnt/β-catenin signaling in rhabdomyosarcoma [PDF]

Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and accounts for about 5% of all malignant paediatric tumours. β-Catenin, a multifunctional nuclear transcription factor in the canonical Wnt signaling pathway, is active in ...
Annavarapu, SR, Ceccarelli, S, Cialfi, S, Dominici, C, Helliwell, TR, Kokai, GK, McDowell, HP, Uccini, S   +7 more
core   +1 more source

Embryonal rhabdomyosarcoma at an unusual age and in an atypical site: a case report

Journal of Medical Case Reports
Background Rhabdomyosarcoma is classified into histologic subtypes: embryonal, alveolar, pleomorphic, spindle, and mixed-type. Embryonal rhabdomyosarcoma is mainly a disease of children. It occurs rarely in adults.
Ayla Kouli, Mouna Baddoura, Miriam Laflouf, Seham Sulaiman   +3 more
doaj   +1 more source

High grade sarcoma, with predominant neuroectodermal and minor embryonal rhabdomyosarcomatous tumor of the uterus: A case report

Gynecologic Oncology Reports, 2019
Background: There have been few documented cases of combined primitive neuroectodermal and embryonal rhabdomyosarcomas (ERMS) in the uterus. Due to their rarity, there is no consensus on the optimal treatment for patients with primitive neuroectodermal ...
Leona Chang, Miriam Enriquez, Nati Lerman, Robin Wilson-Smith   +3 more
doaj   +1 more source