Primary retroperitoneal carcinosarcoma in a child: a case report.

World J Surg Oncol

Special treatment department, Eastern Hepatobiliary Surgery Hospital, 225 Changhai Road, Shanghai 200438, China.

Published: November 2010


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000840PMC
http://dx.doi.org/10.1186/1477-7819-8-99DOI Listing

Publication Analysis

Top Keywords

retroperitoneal carcinosarcoma
12
primary retroperitoneal
8
carcinosarcoma rare
8
carcinosarcoma
5
carcinosarcoma child
4
child case
4
case report
4
report carcinosarcoma
4
rare biphasic
4
biphasic malignancy
4

Similar Publications

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 PDF

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 PDF

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 PDF

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 PDF
Article Synopsis
  • Advanced malignancies in the lower abdomen can invade surrounding spaces and metastasize to lymph nodes, leading to complex cases of paraaortic and pelvic tumors (PPT).
  • A study presents 7 cases over 16 years where aggressive resection of malignant PPTs was performed alongside synthetic arterial graft (SAG) reconstruction of the abdominal aorta and iliac arteries.
  • The outcomes show that this surgical approach is safe, effective in achieving clear margins, maintains patency of grafts long-term, and demonstrates promising long-term oncological results, suggesting its viability in managing malignant PPTs.
View Article and Find Full Text PDF