A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment

Retroperitoneal sarcomas are rare neoplasms that account for only 1%-2% of all solid tumors and liposarcomas represent the most frequent histological type. We describe the case of a 44-year-old female with a retroperitoneal myxoid liposarcoma of 22 × 19 × 8 cm in size. The only symptoms were persist...

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Main Authors: Emanuele Grasso, Fabio Marino, Michele Bottalico, Michele Simone
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Case Reports in Surgery
Online Access:http://dx.doi.org/10.1155/2014/572805
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author Emanuele Grasso
Fabio Marino
Michele Bottalico
Michele Simone
author_facet Emanuele Grasso
Fabio Marino
Michele Bottalico
Michele Simone
author_sort Emanuele Grasso
collection DOAJ
description Retroperitoneal sarcomas are rare neoplasms that account for only 1%-2% of all solid tumors and liposarcomas represent the most frequent histological type. We describe the case of a 44-year-old female with a retroperitoneal myxoid liposarcoma of 22 × 19 × 8 cm in size. The only symptoms were persistent pain and progressive tenderness of the abdomen lasting for two months. The mass was radically excised during laparotomy. CT and MRI were useful to clarify the site of origin of the tumor, relationships with other organs, and planning surgery but final diagnosis was based on histological findings. Here we review the literature about the challenging diagnosis, treatment, and prognostic factors of this disease.
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institution Kabale University
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series Case Reports in Surgery
spelling doaj-art-3a15fe849a9a4b44a9e3c9366d6cf38b2025-02-03T01:12:58ZengWileyCase Reports in Surgery2090-69002090-69192014-01-01201410.1155/2014/572805572805A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and TreatmentEmanuele Grasso0Fabio Marino1Michele Bottalico2Michele Simone3Department of General Surgery, Casa di Cura Santa Maria, Via De Ferrariis 22, 70124 Bari, ItalyDepartment of General Surgery, Casa di Cura Santa Maria, Via De Ferrariis 22, 70124 Bari, ItalyDepartment of Urology, Casa di Cura Santa Maria, Bari, ItalyDepartment of General Surgery, Casa di Cura Santa Maria, Via De Ferrariis 22, 70124 Bari, ItalyRetroperitoneal sarcomas are rare neoplasms that account for only 1%-2% of all solid tumors and liposarcomas represent the most frequent histological type. We describe the case of a 44-year-old female with a retroperitoneal myxoid liposarcoma of 22 × 19 × 8 cm in size. The only symptoms were persistent pain and progressive tenderness of the abdomen lasting for two months. The mass was radically excised during laparotomy. CT and MRI were useful to clarify the site of origin of the tumor, relationships with other organs, and planning surgery but final diagnosis was based on histological findings. Here we review the literature about the challenging diagnosis, treatment, and prognostic factors of this disease.http://dx.doi.org/10.1155/2014/572805
spellingShingle Emanuele Grasso
Fabio Marino
Michele Bottalico
Michele Simone
A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
Case Reports in Surgery
title A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
title_full A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
title_fullStr A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
title_full_unstemmed A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
title_short A Case of Myxoid Liposarcoma of the Retroperitoneum: A Challenging Tumour for Diagnosis and Treatment
title_sort case of myxoid liposarcoma of the retroperitoneum a challenging tumour for diagnosis and treatment
url http://dx.doi.org/10.1155/2014/572805
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