نتایج جستجو برای: rhabdomyosarcoma

تعداد نتایج: 21356  

Journal: :Molecular cancer research : MCR 2013
Hok Khim Fam Cheryl Walton Sheetal A Mitra Miraj Chowdhury Nichola Osborne Kunho Choi Guobin Sun Patrick C W Wong Maureen J O'Sullivan Gulisa Turashvili Samuel Aparicio Timothy J Triche Mason Bond Catherine J Pallen Cornelius F Boerkoel

UNLABELLED Rhabdomyosarcoma is the most common soft tissue sarcoma in children. Metastatic rhabdomyosarcoma in children has a 5-year event-free survival rate of <30%, and a recent clinical trial with irinotecan, a topoisomerase I inhibitor, failed to improve outcome. Therefore, it was surmised that failure of irinotecan may be the result of overexpression of the DNA repair enzyme tyrosyl-DNA ph...

2016
Somen Misra Kunal Patil Neeta Misra

Rhabdomyosarcoma is a malignant neoplasm of primitive mesenchyme exhibiting skeletal muscle differentiation. Rhabdomyosarcoma, which can histopathologically be of embryonal, alveolar, botryoid and pleomorphic types; is a rare tumor in children, with an annual incidence of 4.3 cases per million. Pleomorphic rhabdomyosarcomas is a rare variant, occurring more commonly in adults. We report a rare ...

2016
Hans-Ulrich Schildhaus Suvi Lokka Werner Fenner Jens Küster Ingrid Kühnle Ernst Heinmöller

BACKGROUND Embryonal rhabdomyosarcoma of the prostate in an adult is a very rare event with only a few cases published. Diagnosis usually occurs with advanced disease frequently already with metastatic spread. In adults prognosis is very poor, therefore early diagnosis is crucial. To date, only three cases of spindle cell subtype of embryonal rhabdomyosarcoma of the prostate in an adult have be...

Journal: :Facial plastic surgery clinics of North America 2014
Sherard A Tatum

Rhabdomyosarcoma is the most common soft tissue sarcoma in infants and children. The peak incidence of rhabdomyosarcoma occurs in children between 2 and 5 years of age, and a second peak is seen in teenagers between 15 and 19 years of age. In the final report of 686 patients from the First Intergroup Rhabdomyosarcoma Study (IRS), the median age at diagnosis for a child presenting with rhabdomyo...

Journal: :The British journal of radiology 2004
C W Mak C K Chou C C Su S K Huan J M Chang

Rhabdomyosarcoma is the most common tumour of the lower genitourinary tract in children in the first two decades. Paratesticular rhabdomyosarcoma is associated with a significantly better outcome than lesions elsewhere in the genitourinary tract. Although ultrasound is considered the imaging modality of choice for evaluating intrascrotal pathology, the ultrasound appearance of paratesticular rh...

2011
Young Eun Bahn Sang Kwon

dren and they are far less frequent in adults. Histologically, they are classified into three subtypes: embryonal, alveolar and pleomorphic. While the head and neck are the principal locations for childhood rhabdomyosarcoma, head and neck rhabdomyosarcoma is rare in adults (1). The overall survival is worse for adults than for children (2). The major sites of metastases are lung, bone, bone mar...

Journal: :Oncology reports 2009
Takao Matsubara Katsuyuki Kusuzaki Akihiko Matsumine Hiroaki Murata Haruhiko Satonaka Ken Shintani Tomoki Nakamura Hajime Hosoi Tomoko Iehara Toru Sugimoto Atsumasa Uchida

Rhabdomyosarcoma is a common malignant soft tissue that frequently involves bone and major neurovascular structures and resection of deep-seated rhabdomyosarcoma can cause severe dysfunction in the affected limbs. Based on the mouse osteosarcoma model, we developed a new surgical approach involving photodynamic surgery (PDS), photodynamic therapy (PDT) and radiodynamic therapy (RDT) using acrid...

Journal: :journal of research in medical sciences 0
santosh kumar mondal palash kumar mandal anindya adhikari bijan basak

primary sarcoma of the breast is very rare and constitutes less than 1% of all breast cancers. herein, we report a case of pleomorphic rhabdomyosarcoma (prms) of the right breast in a 49-year-old female patient presented with a mass (7 cm × 6.5 cm). mammography and ultrasonography suspected a malignant lesion and a diagnosis of poorly differentiated carcinoma was made on fine needle aspiration ...

Journal: :iranian journal of radiation research 0
sh. fang department of ultrasound, the affiliated hospital of qingdao university medical college, 16 jiang su road, qingdao, shandong province 266003, china y. sun department of ultrasound, the affiliated hospital of qingdao university medical college, 16 jiang su road, qingdao, shandong province 266003, china m.p.h. yuan wang the university of texas medical school at houston, houston, texas, u.s.a.

primary rhabdomyosarcoma (rms) of the kidney is a rare malignant mesenchymal tumor with an aggressive clinical course. adult renal rms is typically a pleomorphic histologic subtype and only a few cases have ever been reported. we herein present a new case of renal rms of the embryonal histologic subtype in a 26-year-old woman.

2013

Introduction: Rhabdomyosarcoma is the commonest soft tissue sarcoma of childhood. The tumour commonly occurs in the body regions of the head and neck, genitourinary and extremities. Primary rhabdomyosarcoma of the breast is extremely rare and present diagnostic challenges especially in resource limited centers. It is an aggressive tumour with a poor prognosis especially when diagnosed late. Cas...

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