Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2024 Jun 4;16(6):e61642.
doi: 10.7759/cureus.61642. eCollection 2024 Jun.

A Gastrointestinal Stromal Tumor (GIST) and a Pseudocyst of the Pancreas: A Peculiar Case of Both Co-existing in the Same Patient

Affiliations
Case Reports

A Gastrointestinal Stromal Tumor (GIST) and a Pseudocyst of the Pancreas: A Peculiar Case of Both Co-existing in the Same Patient

Manwar S Ali et al. Cureus. .

Abstract

Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasms of the gastrointestinal (GI) tract, typically originating from the interstitial cells of Cajal. The clinical presentations are variable according to their size and shape but rarely present as a palpable abdominal mass. Pancreatic pseudocysts are common complications of chronic pancreatitis characterized by fluid collections surrounded by a non-epithelialized wall of fibrous and granulation tissue. Patients may present with non-specific symptoms like abdominal pain, nausea, and vomiting and they generally have a history of acute pancreatitis. Small pseudocysts often resolve spontaneously, but larger ones often become symptomatic and may lead to complications. It is rare to find both a GIST of the stomach and a pseudocyst of the pancreas in the same patient. We present a unique case of a giant GIST and a pancreatic pseudocyst in a 72-year-old male who was experiencing abdominal pain and distension. Imaging revealed a massive lesion originating from the posterior gastric wall, which resembled a pseudocyst, along with a distinct cystic lesion adjacent to the pancreatic body. During surgical exploration, a complex interplay of both pathologies was discovered, requiring a comprehensive resection approach. The successful outcome highlights the importance of careful evaluation and personalized management in such rare cases.

Keywords: cyst; gastrointestinal stromal tumor (gist); mesenchymal tumors; pancreatic pseudocyst; stomach.

PubMed Disclaimer

Conflict of interest statement

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Figures

Figure 1
Figure 1. Pre-operative images of the abdomen (A) Front view and (B) lateral view.
Figure 2
Figure 2. Intra-operative images. (A) Intra-operative mass arising from the posterior wall of the stomach. (B) Distal pancreatectomy done for the pseudocyst arising from the body and tail of the pancreas. (C) After resection of the intra-operative mass.
Figure 3
Figure 3. GIST arising from the posterior wall of the stomach. (A) Section from the gastric mass showing normal compressed gastric mucosa at one end and the tumor arising in the submucosa and muscularis propria. (B) The tumor is composed of cells arranged in nodules separated by fibrous stroma. (C) The cells are immunopositive for cKIT. (D) The tumor cells are immunopositive for DOG1.
GIST: Gastrointestinal stromal tumor
Figure 4
Figure 4. Pseudocyst arising from the body and tail of the pancreas. (A) A section of the cyst shows a fibro-collagenous wall. (B) The cyst does not have a lining epithelium. Its lumen shows inflammatory granulation tissue, plasma cells, and histiocytes.

Similar articles

Cited by

References

    1. Gastrointestinal stromal tumor (GIST) Joensuu H. https://www.sciencedirect.com/science/article/pii/S0923753419637014 Ann Oncol. 2006;1:280–286. - PubMed
    1. Giant gastrointestinal stromal tumor (GIST) of the stomach cause of high bowel obstruction: surgical management. Cappellani A, Piccolo G, Cardì F, et al. https://link.springer.com/article/10.1186/1477-7819-11-172. World J Surg Oncol. 2013;11:172. - PMC - PubMed
    1. Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors. Hirota S, Isozaki K, Moriyama Y, et al. https://www.science.org/doi/abs/10.1126/science.279.5350.577. Science. 1998;279:577–580. - PubMed
    1. A gist of gastrointestinal stromal tumors: a review. Rammohan A, Sathyanesan J, Rajendran K, et al. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3708046/ World J Gastrointest Oncol. 2013;5:102–112. - PMC - PubMed
    1. Giant gastrointestinal stromal tumor presenting as a palpable abdominal mass: an unusual presentation. Patil S, Jain S, Kaza RC, Chamberlain RS. https://www.hindawi.com/journals/isrn/2011/894829/ Int Sch Res Notices. 2011;2011:894829. - PMC - PubMed

Publication types

LinkOut - more resources