نتایج جستجو برای: embryonal rhabdomyosarcoma

تعداد نتایج: 24466  

Introduction: Rhabdomyosarcoma is the most frequently occurring intrusive soft tissue sarcoma in the pediatric age group. Orbit is the most common location for a pediatric rhabdomyosarcoma, but it can occur in the oral cavity, pharynx, face and neck in the descending order of incidence. Rhabdomyosarcoma in the ear is extremely rare.   Case Report: A 5-year-old girl prese...

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.

Journal: :iranian journal of pathology 2014
mary mathew padmapriya jaiprakash lakshmi rao nalini bhaskaranand

congenital or neonatal rhabdomyosarcoma is a rare entity, usually presenting as masses in the head and neck region as well as genitourinary tract. the embryonal variant is the most common type occurring in infancy. this is a case of congenital rhabdomyosarcoma with a huge forearm mass, with metastatic discrete nodules in the soft tissues of the neck and scapular region, resembling a ‘blueberry ...

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...

2004
NORMAN ASHTON

smNopsis A series of 34 cases of embryonal sarcoma and embryonal rhabdomyosarcoma of the orbit has been placed histologically into three groups according to their maximum degree of differentiation at any stage: (a) embryonal sarcoma, (b) non-striated embryonal rhabdomyosarcoma, and (c) striated embryonal rhabdomyosarcoma. The patients were then followed up. This paper presents a summary of the ...

Lakshmi Rao Mary Mathew Nalini Bhaskaranand Padmapriya Jaiprakash,

Congenital or neonatal rhabdomyosarcoma is a rare entity, usually presenting as masses in the head and neck region as well as genitourinary tract. The embryonal variant is the most common type occurring in infancy. This is a case of congenital rhabdomyosarcoma with a huge forearm mass, with metastatic discrete nodules in the soft tissues of the neck and scapular region, resembling a ‘blueberry ...

Journal: :iranian red crescent medical journal 0
yining li department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china zhongying fu department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china weilun chen department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china lixin yang department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china wei zhu department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china; department of otolaryngology and head and neck surgery, the first hospital of jilin university, changchun, china. tel: +86-13756661259, fax: +86-043184808105

case presentation herein, we reported a case of a 22-year-old woman diagnosed with erms, t1n0m0 stage, localized at the right vocal cord. tumor was successfully treated with a radical excision and selective neck dissection and followed-up for 5 years with no evidence of local recurrence. introduction although embryonal rhabdomyosarcomas (erms) represent the most common (50% - 60%) clinical form...

2016
Maryam Sadat Hosseini Tahereh Ashrafganjoei Ainaz Sourati Morteza Tabatabeifar Mahdiss Mohamadianamiri

INTRODUCTION Rhabdomyosarcoma has known as a highly malignant soft tissue sarcoma. It has been the most common soft tissue sarcoma in childhood, accounting for about 3 to 4 % of all cases of childhood cancer. Rhabdomyosarcoma was rare in adults, accounting for 3% of all soft-tissue sarcomas. embryonal rhabdomyosarcoma of female genital tract including uterine cervix in an adult was rare. CASE...

Journal: :American journal of clinical pathology 2008
Jian Wang Xiaoyu Tu Weiqi Sheng

We report 5 cases of sclerosing rhabdomyosarcoma. The patients included 4 adults and 1 adolescent. In the 5 cases, 3 tumors occurred in the head and neck region and 2 in an extremity. Histologically, all 5 tumors were characterized by the presence of abundant extracellular hyaline matrix, mimicking osteoid or chondroid tissue. They were composed mostly of primitive small round cells that displa...

Journal: :Journal of clinical pathology 1985
J A Royds S Variend W R Timperley C B Taylor

A comparative study of beta enolase and myoglobin as markers of muscle differentiation in rhabdomyosarcoma was carried out, using an immunoperoxidase peroxidase antiperoxidase technique. Material from 26 cases of childhood rhabdomyosarcoma was studied and subdivided into embryonal and alveolar types. Positive cytoplasmic staining for beta enolase was seen in 85% of tumours studied (91% alveolar...

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