Coexistence of gastric gastrointestinal stromal tumor, intro-abdominal and retroperitoneal liposarcomas –a case report
- 243 Downloads
Gastric gastrointestinal stromal tumor (GIST), intro-abdominal and retroperitoneal neoplasms are distinct tumors arising from different cell layers; therefore, coexistence of such tumors is relatively rare.
A man complained of early satiety for 2 mouths, whose upper gastrointestinal (GI) endoscopy showed a tumor arising from the greater curvature of gastric body and extending into the lumen. Abdominal computed tomography (CT) revealed coexistence of gastric, intro-abdominal and retroperitoneal masses. Wedge resection for gastric tumor, resection for intro-abdominal and retroperitoneal tumors were done. The postoperative histological examination suggested simultaneous development of a gastric GIST, intro-abdominal and retroperitoneal myxoid liposarcomas.
Although both GISTs and liposarcomas originate from mesenchymal tissues, simultaneous development of a gastric GIST, intro-abdominal and retroperitoneal liposarcomas is the first such case to be reported in the literature.
KeywordsGIST Intro-abdominal liposarcoma Retroperitoneal liposarcoma Myxoid liposarcoma
Gastrointestinal stromal tumor
World Health Organization
Past decades have witnessed frequent cases of synchronous occurrence of a GIST and another neoplasms [1, 2]. However, gastric GISTs simultaneous development of a liposarcoma is rarely reported. Liposarcoma represents 20–30% of adult soft tissue tumors, most commonly -arising from the extremities, followed by the retroperitoneum . Furthermore, its abdominal localization occurs only in 5% of cases . Although both GISTs and liposarcomas originate from mesenchymal tissues, simultaneous development of a gastric GIST, intro-abdominal and retroperitoneal liposarcomas is extremely rare in the literature.
A 56-year-old male with early satiety for 2 mouths was admitted to our hospital. There was no history of weight loss, without relevant past and family history. An 18*25 cm oval tumor with medium texture was palpable below the left costal margin during the physical examination.
A surgical operation was performed. Intraoperatively, a huge oval lobulated oozing soft mass (about 18.0*25.0*15.0 cm) originating from the descending colon mesentery was identified. A tumor (about 2.5*2.0*2.0 cm) at the greater curvature of gastric body and a tumor (about 5.0*4.0*2.5 cm) close to the left psoas were detected. Adjacent to the anterior wall of the abdominal aorta, the intro-abdominal tumor was surrounded by the small bowel and left hemicolon. The round-like lobulated retroperitoneal tumor was found among the left psoas, left iliac vessels, sigmoid colon and intro-abdominal tumor. The tumors were well-circumscribed from the surrounding organs and without signs of infiltrating tumor growth. Furthermore, the tumors were not related to the adjacent major vessels, without the detection of distant metastasis or nodal involvement. Wedge resection for gastric tumor, complete resection for intro-abdominal and retroperitoneal tumors were performed.
GISTs, comprising about 0.1–3% of all gastrointestinal malignant tumors, are rare.These tumors, strongly expressing the c-KIT protein (CD117; a type III tyrosine kinase receptor encoded by the c-kit proto-ongogene), are identified as arise from interstitial cells of Cajal or their precursors . As one of the most common mesenchymal neoplasms of the gastrointestinal tract, GISTs arise mainly from the stomach, small bowel and duodenum. Although GISTs usual present with alimentary tract hemorrhage, abdomen mass, abdominal pain and gastrointestinal obstruction, one-third of all cases are found incidentally. As shown in our case, based on the tumor detected during gastrointestinal endoscopy and CT scans due to the symptoms related to the huge liposarcoma, the gastric GIST could be classified as an incidental tumor.
According to the World Health Organization (WHO), lipomatous tumors were classified into well-differentiated, myxoid, pleomorphic and dedifferentiated subtypes . Myxoid liposarcoma, a common subtype, is usually asymptomatic, incidentally identified, which occurs most commonly in deep soft tissues of the extremities while uncommon sites include the head and neck, thorax, and subcutis .The retroperitoneum is the most frequent site of liposarcoma. Up to 40% of liposarcomas occur in the intro-abdominal localization while those originated from the mesentery are rare. It is worth noting that primary retroperitoneal myxoid liposarcomas have been considered rare or even nonexistent , according to the recent studies. Furthermore, clinicopathologic studies confirmed that myxoid liposarcomas prefer to metastasize to deep soft tissues or bones, and the retroperitoneum stands for one of the most common metastatic locations . As shown in our case, retroperitoneal liposarcoma could be considered as a metastatic mass from intro-abdominal myxoid liposarcoma.
Both GISTs and liposarcomas arise from mesenchymal tissues, coincidence of which is rarely reported. We only found two previously reported cases in the literature [8, 9]. One case showed a gastric GIST coexistence of a retroperitoneal liposarcoma , while the other reported a case of coincident abdominal carcinoid tumor, GIST and well-differentiated liposarcoma in a NF1 patient . Various hypotheses including gene mutations, expression of metallothioneins (MT) and influenced neighboring tissues by the same carcinogen have been used to explain the simultaneous development of a GIST and other carcinomas [10, 11]. It is worth noting that genetic changes and polymorphisms play an important role in the development of sarcomas . Furthermore, there is emerging data on genetic polymorphisms associated with susceptibility to a wide range of neoplasms [13, 14], which can be reasonably explained by genetic changes and polymorphisms.
Radical surgery is the main treatment for all mesenchymal tumors. Standing for the only curable chance for primary GIST, surgical resection can be achieved by only a wedge resection of the stomach or a segmental resection of the small bowel, while extensive surgery is occasionally performed for larger or poorly positioned GISTs . Surgical resection is the only effective treatment for liposarcoma. During the procedure, the tissues or the organs adherent to the tumor usually need to be removed . Even debulking surgery is sometimes helpful to treat with nettlesome symptoms of recurrence or un-resectable liposarcoma . However, debulking surgery is not recommended in the recurrent or un-resectable GIST and for these patients, tyrosine-kinase inhibitor is a reasonable choice. In our case, the patient was diagnosed as simultaneous development of low grade gastric GIST, intro-abdominal andretroperitoneal myxoid liposarcomas. The evidence supporting the application of chemotherapy and radiotherapy for liposarcoma is limited . A retrospective study showed a good local control rate for myxoid liposarcoma patients accepting surgery and radiotherapy , thereby, the patient was suggested to accept radiotherapy. The patient received CT scans twice a year, displaying no evidence of tumor recurrence in a follow up period of 15 months, making a long follow-up period necessary.
We wish to thank pathologists Dr. Hai-ou Zhao for his contribution in the preparation of pathology images used in this report.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
YZ and XW compiled all information relating to the patient and wrote the manuscript. QS, CX and JJ were involved in data interpretation and manuscript preparation. All authors read and approved the final manuscript.
Ethics approval and consent to participate
The study was reviewed and approved by the Yancheng City No. 1 People’s Hospital Institutional Review Board.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and accompanying images.
No potential conflicts of interest were disclosed.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- 9.James AW, Chang L, Genshaft S, Dry SM. Coincident liposarcoma, carcinoid and gastrointestinal stromal tumor complicating type 1 neurofibromatosis: Case report and literature review. J Orthop. 2013;12(Suppl 1):S111–6.Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.