Southern Clinics of Istanbul Eurasia (Jan 2018)

Primary Duodenal Mucosa-Associated Lymphoid Tissue Lymphoma (MALToma): A Case Report

  • Arzu Cennet Işık,
  • Seydahmet Akın,
  • Mesut Ayer,
  • Tuğba Sevinç Gamsız,
  • Begüm Damla Şencan,
  • Özcan Keskin

DOI
https://doi.org/10.14744/scie.2018.35220
Journal volume & issue
Vol. 28, no. 4
pp. 297 – 299

Abstract

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Primary duodenal mucosa-associated lymphoid tissue (MALT) lymphoma is the most rarely seen type of non-Hodgkin lymphoma and is diagnosed most commonly in the stomach. A 20-year-old male patient presented with progressive vomiting, weight loss, and abdominal pain. There was nothing remarkable on 2 consecutive gastroduodenoscopies, but his complaints persisted. A double-contrast barium examination was performed, which revealed a filling defect in the duodenum. A biopsy specimen from the patient determined the presence of Helicobacter pylori and the patient was diagnosed with poorly-differentiated B-cell MALT lymphoma Successful chemotherapy and H. pylori eradication therapy were performed and follow-up revealed no recurrence.

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