A Case of Primary Duodenal Liposarcoma

Soft tissue sarcomas are common neoplasms accounting for 1% of all adult malignancies; however, soft tissue sarcomas infrequently arise from the abdominal viscera. Many case reports discuss gastric and esophageal neoplasms. In the group of gastrointestinal liposarcomas, primary duodenal liposarcomas...

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Main Authors: Zachary Whitham, Aaron Blackham, Victoria Loven
Format: Article
Language:English
Published: Karger Publishers 2020-06-01
Series:Case Reports in Oncology
Subjects:
Online Access:https://www.karger.com/Article/FullText/507479
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spelling doaj-9e931cec3cfa416088cdc28f21c692732020-11-25T03:25:10ZengKarger PublishersCase Reports in Oncology1662-65752020-06-0113264965410.1159/000507479507479A Case of Primary Duodenal LiposarcomaZachary WhithamAaron BlackhamVictoria LovenSoft tissue sarcomas are common neoplasms accounting for 1% of all adult malignancies; however, soft tissue sarcomas infrequently arise from the abdominal viscera. Many case reports discuss gastric and esophageal neoplasms. In the group of gastrointestinal liposarcomas, primary duodenal liposarcomas are among the rarest, with only three previous cases reported in the literature. Herein, we discuss a case of primary duodenal liposarcoma. A 59-year-old woman presented with symptoms consistent with anemia raising suspicion for an upper gastrointestinal bleed. Upper endoscopy revealed an ulcerated mass in the first portion of the duodenum. The patient underwent a segmental duodenal resection and distal gastrectomy with Roux-en-Y reconstruction. A diagnosis of dedifferentiated liposarcoma was rendered on the resected specimen. At 16 months’ follow-up, the patient remains without evidence of disease recurrence. We have presented a case of primary duodenal liposarcoma, which is among the rarest locations for gastrointestinal sarcomas with only three previous reports in the literature. Liposarcomas should be included in the differential for submucosal masses of the duodenum.https://www.karger.com/Article/FullText/507479duodenumliposarcomasarcoma
collection DOAJ
language English
format Article
sources DOAJ
author Zachary Whitham
Aaron Blackham
Victoria Loven
spellingShingle Zachary Whitham
Aaron Blackham
Victoria Loven
A Case of Primary Duodenal Liposarcoma
Case Reports in Oncology
duodenum
liposarcoma
sarcoma
author_facet Zachary Whitham
Aaron Blackham
Victoria Loven
author_sort Zachary Whitham
title A Case of Primary Duodenal Liposarcoma
title_short A Case of Primary Duodenal Liposarcoma
title_full A Case of Primary Duodenal Liposarcoma
title_fullStr A Case of Primary Duodenal Liposarcoma
title_full_unstemmed A Case of Primary Duodenal Liposarcoma
title_sort case of primary duodenal liposarcoma
publisher Karger Publishers
series Case Reports in Oncology
issn 1662-6575
publishDate 2020-06-01
description Soft tissue sarcomas are common neoplasms accounting for 1% of all adult malignancies; however, soft tissue sarcomas infrequently arise from the abdominal viscera. Many case reports discuss gastric and esophageal neoplasms. In the group of gastrointestinal liposarcomas, primary duodenal liposarcomas are among the rarest, with only three previous cases reported in the literature. Herein, we discuss a case of primary duodenal liposarcoma. A 59-year-old woman presented with symptoms consistent with anemia raising suspicion for an upper gastrointestinal bleed. Upper endoscopy revealed an ulcerated mass in the first portion of the duodenum. The patient underwent a segmental duodenal resection and distal gastrectomy with Roux-en-Y reconstruction. A diagnosis of dedifferentiated liposarcoma was rendered on the resected specimen. At 16 months’ follow-up, the patient remains without evidence of disease recurrence. We have presented a case of primary duodenal liposarcoma, which is among the rarest locations for gastrointestinal sarcomas with only three previous reports in the literature. Liposarcomas should be included in the differential for submucosal masses of the duodenum.
topic duodenum
liposarcoma
sarcoma
url https://www.karger.com/Article/FullText/507479
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