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Endoscopic mucosal resection confirms rare gastric plasmacytoma in 53-year-old manRare Gastric Plasmacytoma Diagnosed After Acid Reflux Workup

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Key Takeaway
Consider gastric plasmacytoma in patients with atypical gastric lesions; EMR can aid diagnosis.

This is a case report of a 53-year-old man presenting with acid reflux and heartburn who was found to have a primary solitary gastric plasmacytoma after undergoing endoscopic mucosal resection (EMR). The diagnosis was confirmed through histopathology, immunohistochemistry, bone marrow aspiration, serum and urine free light chain assays, and PET-CT, ruling out multiple myeloma and other plasma cell disorders. The report highlights the role of EMR in obtaining tissue for definitive diagnosis of this rare extramedullary plasmacytoma.

The authors note that gastric plasmacytoma is an uncommon presentation of plasma cell neoplasms, and this case adds to the limited literature. Key limitations include the single-patient design, which precludes any conclusions about treatment efficacy or prognosis. Follow-up duration and long-term outcomes were not reported.

For clinicians, this report serves as a reminder to consider plasma cell tumors in the differential diagnosis of gastric lesions, especially when endoscopic findings are atypical. However, practice recommendations cannot be drawn from a single case. Further studies with larger cohorts are needed to establish diagnostic and management guidelines.

A 53-year-old man with acid reflux and heartburn was found to have a rare tumor called a gastric plasmacytoma. This is a type of plasma cell cancer that starts in the stomach lining. Doctors used a procedure called endoscopic mucosal resection (EMR) to remove the growth and confirm the diagnosis.

The diagnosis was backed by several tests: tissue analysis, special stains, bone marrow aspiration, blood and urine tests for abnormal proteins, and a PET-CT scan. All pointed to a solitary plasmacytoma, meaning the cancer was limited to one spot in the stomach.

Because this is a single case report, the findings are very limited. Case reports describe one person's experience and cannot be generalized to others. No information on treatment outcomes, side effects, or long-term follow-up was provided.

For readers, this report highlights that rare tumors can sometimes be discovered during routine care for common symptoms like heartburn. However, it does not change standard medical practice. Anyone with persistent digestive symptoms should discuss them with their doctor.

What this means for you:
A rare stomach tumor was found in one patient; this does not change standard care.

Common questions

What is a gastric plasmacytoma?

It is a rare tumor made of plasma cells that occurs in the stomach. In this case, it was solitary, meaning only one tumor was found.

How was the diagnosis confirmed?

Doctors used several tests: tissue analysis, immunohistochemistry, bone marrow aspiration, blood and urine tests for abnormal proteins, and a PET-CT scan.

Is this cancer common?

No, gastric plasmacytoma is very rare. This report describes only one case, so it does not tell us how common it is in the general population.

Should I worry about this if I have heartburn?

No. Heartburn is very common and usually not caused by a tumor. This single case does not change what doctors recommend for typical acid reflux.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedJul 2026
View Original Abstract ↓
Extramedullary plasmacytoma (EMP) is a rare plasma cell malignancy, accounting for approximately 3% of all plasma cell neoplasms. Gastric plasmacytoma, a distinct subtype of EMP arising from B lymphocytes, is extremely uncommon, representing roughly 2% of EMP cases, and lacks specific clinical manifestations. Herein, we report a 53-year-old male presenting with persistent acid reflux and heartburn. Gastroscopy identified a flat, elevated lesion in the gastric body. Endoscopic mucosal resection (EMR) was performed to obtain the lesion specimen. The diagnosis of primary solitary gastric plasmacytoma was confirmed via histopathology, immunohistochemistry, bone marrow aspiration, serum and urine free light chain assays, and positron emission tomography–computed tomography (PET-CT). We further review the clinical features, diagnostic approaches, therapeutic strategies, and prognosis of this disease, aiming to provide a reference for the diagnosis and management of rare gastric plasma cell tumors in clinical practice.
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