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Carcinosarcoma is a rare biphasic malignancy consisting of intermixed epithelial and mesenchymal elements. Carcinosarcoma is particularly rare among children. We accepted a 7 year old patient with retroperitoneal carcinosarcoma. The tumor was totally resected and no recurrence is found 11 months after operation. Literatures has been reviewed and there are few reports of primary retroperitoneal carcinosarcoma in children up to date. So we report the patient's clinical character, surgical resection, pathological and immunohistochemical analysis.
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http://dx.doi.org/10.1186/1477-7819-8-99 | DOI Listing |
Int J Gynaecol Obstet
June 2025
Department of Internal Medicine, Division of Hematology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
The aim of the present study was to evaluate the occurrence of synchronous or metachronous hematologic and gynecologic malignancies. The medical database of the pathology department at a tertiary center was searched from 2016 to 2024 for cases involving both hematologic and gynecologic tumors. A literature search using Google Scholar and PubMed was also conducted between May and June 2024.
View Article and Find Full Text PDFNihon Hinyokika Gakkai Zasshi
April 2025
Department of Urology, Sapporo Medical University School of Medicine.
We present a case of retroperitoneal carcinosarcoma. A 48-year-old woman with left-sided abdominal pain and a 15 cm tumor in the lower left renal retroperitoneal region on computed tomography (CT) was referred to our hospital. Contrast-enhanced CT showed a well-defined tumor with contrast effect on the retroperitoneum.
View Article and Find Full Text PDFCurr Probl Cancer
December 2023
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Muğla Sıtkı Koçman University, Faculty of Medicine, Muğla, Turkey.
To investigate the risk factors for occult omental metastasis and the effect of omentectomy on the survival of type 2 endometrial cancer (EC) patients. This study enrolled patients who were diagnosed with high-risk (grade 3, serous, clear cell, undifferentiated, carcinosarcoma, or mixed type) EC between 2000 and 2021 and underwent surgery in our center. Data from 482 patients were analyzed retrospectively.
View Article and Find Full Text PDFDiagnostics (Basel)
October 2022
Department of Hematology/Oncology, Georgia Cancer Center, Augusta, GA 30912, USA.
Adrenal cortical carcinosarcomas are a rare and typically aggressive malignancy with few reported cases in medical literature. We present a case of a 78-year-old female who presented with complaints of fatigue and right shoulder pain. Imaging of the abdomen with computed tomography visualized a large mass in the right upper quadrant.
View Article and Find Full Text PDFAm J Case Rep
May 2021
Department of Surgery, Shiga General Hospital, Moriyama, Shiga, Japan.