Embryonal rhabdomyosarcoma of the cervix with focal pleomorphic areas

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Sarcoma botryoides (embryonal rhabdomyosarcoma) of the uterine cervix in sisters.

Sarcoma botryoides (embryonal rhabdomyosarcoma) rarely arises in the uterine cervix. We report a case of a 14-year-old female with sarcoma botryoides who presented with prolonged vaginal bleeding and cervical polyp. The biopsy specimen confirmed sarcoma botryoides. The patient underwent radical surgery of the tumor and hysterectomy without adjuvant chemotherapy. The sister of the patient had di...

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Embryonal Rhabdomyosarcoma of the Uterine Cervix: Two Cases Report and Literature Review

Introduction: Embryonal rhabdomyosarcoma (RMS) of the uterine cervix is a rare and extremely aggressive malignant entity. However, prognosis seems to be improved with the use of multimodality approach treatment. Cases: We report the cases of 50and 51-year-old women, presenting with vaginal bleeding and mass. The two patients underwent radical surgery. Histological examination revealed RMS of ut...

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Embryonal Rhabdomyosarcoma of the Cervix: A Rare Disease at an Uncommon Age

Embryonal rhabdomyosarcoma (RMS) is a rare type of sarcoma, primarily seen in the pediatric and adolescent population. Three subtypes of embryonal RMS are described, with the botryoid type being the most common. The incidence of this disease in adult females is 0.4% to 1% with the affected age group being patients in the third to fourth decade of life. It is exceedingly rare in patients above 4...

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Adult Duodenal Pleomorphic Rhabdomyosarcoma

A 73-year-old woman was admitted with severe anemia. An esophagogastroduodenoscopy revealed the presence of a tumor in the second portion of the duodenum (Figure 1); biopsies showed pleomorphic rhabdomyosarcoma (RMS; Figure 2). Phosphotungstic acid-hematoxylin staining highlighted cytoplasmic cross in tumor cells, and immunohistochemical staining demonstrated that the tumor was positive for mus...

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A Case of Embryonal Rhabdomyosarcoma of Cervix Uteri in a 14 Year Old Girl

Rhabdomyosarcoma is an aggressive soft tissue malignancy of childhood and adolescence arising from embryonal mesenchyme [1]. As compared to literature available, these tumours are mainly discussed in context of case studies. Most common affected sites are head, neck, abdomen and genitourinary tract [2]. Embryonal rhabdomyosarcoma is the most common subtype, of which botryoid is a polypoidal var...

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ژورنال

عنوان ژورنال: Journal of Clinical Pathology

سال: 2007

ISSN: 0021-9746

DOI: 10.1136/jcp.2005.034769