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Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association

Desmoplastic small round cell tumors (DSRCTs) are rare and aggressive malignant tumors. The aim of the present study was to analyze computed tomography (CT) and fluorodeoxyglucose positron emission tomography (FDG-PET)/CT imaging features of intra-abdominal desmoplastic DSRCT, and investigate the as...

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Autores principales: CHEN, JINGJING, WU, ZENGJIE, SUN, BINBIN, LI, DACHENG, WANG, ZHENGUANG, LIU, FANGJUN, HUA, HUI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840839/
https://www.ncbi.nlm.nih.gov/pubmed/27123106
http://dx.doi.org/10.3892/ol.2016.4421
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author CHEN, JINGJING
WU, ZENGJIE
SUN, BINBIN
LI, DACHENG
WANG, ZHENGUANG
LIU, FANGJUN
HUA, HUI
author_facet CHEN, JINGJING
WU, ZENGJIE
SUN, BINBIN
LI, DACHENG
WANG, ZHENGUANG
LIU, FANGJUN
HUA, HUI
author_sort CHEN, JINGJING
collection PubMed
description Desmoplastic small round cell tumors (DSRCTs) are rare and aggressive malignant tumors. The aim of the present study was to analyze computed tomography (CT) and fluorodeoxyglucose positron emission tomography (FDG-PET)/CT imaging features of intra-abdominal desmoplastic DSRCT, and investigate the association of these features with histopathological results. The present study was a retrospective investigation of 4 patients with DSRCT. All patients underwent CT and dynamic CT, and 1 additionally underwent FDG-PET/CT scanning. Following a tumor resection, routine hematoxylin and eosin staining, and immunostaining, were performed and evaluated. Multiple large abdominopelvic masses were identified in all 4 patients; however, no indications of their site of origin were demonstrated. CT revealed soft-tissue masses with patchy foci of hypodense lesions. Contrast-enhanced CT revealed slightly or moderately heterogeneous enhancement of the lesions. Other observations from these patients included calcification (n=2), peritoneal seeding (n=3), hepatic metastasis (n=3), retroperitoneal lymphadenopathy (n=3) and ascites (n=2). FDG-PET/CT revealed multiple nodular increased FDG uptake in the abdominopelvic masses, and in the liver and peritoneum in 1 case. Intra-abdominal DSRCT demonstrated significant diagnostic characteristics on plain and contrast-enhanced CT. Multiple, bulky soft-tissue masses inside the peritoneal cavity, particularly in male adolescents and young adults, should be considered as potential cases of DSRCT. FDG-PET/CT techniques may be utilized to aid the staging of tumors.
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spelling pubmed-48408392016-04-27 Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association CHEN, JINGJING WU, ZENGJIE SUN, BINBIN LI, DACHENG WANG, ZHENGUANG LIU, FANGJUN HUA, HUI Oncol Lett Articles Desmoplastic small round cell tumors (DSRCTs) are rare and aggressive malignant tumors. The aim of the present study was to analyze computed tomography (CT) and fluorodeoxyglucose positron emission tomography (FDG-PET)/CT imaging features of intra-abdominal desmoplastic DSRCT, and investigate the association of these features with histopathological results. The present study was a retrospective investigation of 4 patients with DSRCT. All patients underwent CT and dynamic CT, and 1 additionally underwent FDG-PET/CT scanning. Following a tumor resection, routine hematoxylin and eosin staining, and immunostaining, were performed and evaluated. Multiple large abdominopelvic masses were identified in all 4 patients; however, no indications of their site of origin were demonstrated. CT revealed soft-tissue masses with patchy foci of hypodense lesions. Contrast-enhanced CT revealed slightly or moderately heterogeneous enhancement of the lesions. Other observations from these patients included calcification (n=2), peritoneal seeding (n=3), hepatic metastasis (n=3), retroperitoneal lymphadenopathy (n=3) and ascites (n=2). FDG-PET/CT revealed multiple nodular increased FDG uptake in the abdominopelvic masses, and in the liver and peritoneum in 1 case. Intra-abdominal DSRCT demonstrated significant diagnostic characteristics on plain and contrast-enhanced CT. Multiple, bulky soft-tissue masses inside the peritoneal cavity, particularly in male adolescents and young adults, should be considered as potential cases of DSRCT. FDG-PET/CT techniques may be utilized to aid the staging of tumors. D.A. Spandidos 2016-05 2016-04-07 /pmc/articles/PMC4840839/ /pubmed/27123106 http://dx.doi.org/10.3892/ol.2016.4421 Text en Copyright: © Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
CHEN, JINGJING
WU, ZENGJIE
SUN, BINBIN
LI, DACHENG
WANG, ZHENGUANG
LIU, FANGJUN
HUA, HUI
Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title_full Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title_fullStr Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title_full_unstemmed Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title_short Intra-abdominal desmoplastic small round cell tumors: CT and FDG-PET/CT findings with histopathological association
title_sort intra-abdominal desmoplastic small round cell tumors: ct and fdg-pet/ct findings with histopathological association
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4840839/
https://www.ncbi.nlm.nih.gov/pubmed/27123106
http://dx.doi.org/10.3892/ol.2016.4421
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