S5250 An Atypical Presentation of Refractory Peptic Ulcer Disease

Introduction: Peptic ulcer disease (PUD) refractory to standard high dose proton pump inhibitor (PPI) therapy raises concerns for patient non-compliance, rapid CYP metabolizers or an atypical underlying etiology including malignancy or Crohn’s disease. We describe a patient with a refractory gastric ulcer, found to have diffuse large-cell lymphoma (DLBCL). Case Description: A 72-year-old man presented with multiple episodes of gastrointestinal bleeding over 6 months, attributed to PUD despite the use of high-dose PPIs. He was found to have rapid metabolism of CYP2C19 and hence started on vonoprazan. Despite this, he continued to have melena and abdominal pain. Laboratory tests noted a hemoglobin drop from 16.8 to 10.5 within a month. He underwent endoscopy, that showed a large, non-bleeding cratered gastric ulcer with a clean ulcer base (Forrest Class III) in the antrum with benign-appearing, intrinsic severe stenosis immediately distal to the ulcer. Prior endoscopic biopsies were negative. Further workup for the etiology of this ulcer was pursued. CT imaging revealed gastric distension, irregular thickening of the peripyloric region with mildly prominent adjacent lymph nodes. Positron emission tomography-CT showed abnormal 18‐fluorodeoxyglucose uptake within the gastric antrum with a maximum standardized uptake value of 26.7. EUS revealed a hypoechoic intramural (subepithelial) lesion in the antrum appearing to originate from muscularis propria (layer 4), underlying the area of ulceration. Fine needle biopsies were obtained, and pathological findings revealed diffuse proliferation of large atypical lymphoid cells. Immunohistochemical staining was positive for CD10, CD20, BCL6, and MYC. The patient was diagnosed with DLBCL, Not Otherwise Specified (Germinal Center B-cell phenotype) and has started treatment. Discussion: This case demonstrates the importance of evaluating for underlying etiologies in cases with refractory or atypical presentations PUD.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001148460.98431.68
Primary Topic
Diagnosis and treatment of tuberculosis
Type
article
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article

S5250 An Atypical Presentation of Refractory Peptic Ulcer Disease

Mayank Goyal, Ashwariya Ohri, Preeyati Chopra, Ryan Law et al.
The American Journal of Gastroenterology
Diagnosis and treatment of tuberculosis
article

S5250 An Atypical Presentation of Refractory Peptic Ulcer Disease

Mayank Goyal, Ashwariya Ohri, Preeyati Chopra, Ryan Law, Maunil Bhatt, Khushboo Gala
article en

Abstract

Introduction: Peptic ulcer disease (PUD) refractory to standard high dose proton pump inhibitor (PPI) therapy raises concerns for patient non-compliance, rapid CYP metabolizers or an atypical underlying etiology including malignancy or Crohn’s disease. We describe a patient with a refractory gastric ulcer, found to have diffuse large-cell lymphoma (DLBCL). Case Description: A 72-year-old man presented with multiple episodes of gastrointestinal bleeding over 6 months, attributed to PUD despite the use of high-dose PPIs. He was found to have rapid metabolism of CYP2C19 and hence started on vonoprazan. Despite this, he continued to have melena and abdominal pain. Laboratory tests noted a hemoglobin drop from 16.8 to 10.5 within a month. He underwent endoscopy, that showed a large, non-bleeding cratered gastric ulcer with a clean ulcer base (Forrest Class III) in the antrum with benign-appearing, intrinsic severe stenosis immediately distal to the ulcer. Prior endoscopic biopsies were negative. Further workup for the etiology of this ulcer was pursued. CT imaging revealed gastric distension, irregular thickening of the peripyloric region with mildly prominent adjacent lymph nodes. Positron emission tomography-CT showed abnormal 18‐fluorodeoxyglucose uptake within the gastric antrum with a maximum standardized uptake value of 26.7. EUS revealed a hypoechoic intramural (subepithelial) lesion in the antrum appearing to originate from muscularis propria (layer 4), underlying the area of ulceration. Fine needle biopsies were obtained, and pathological findings revealed diffuse proliferation of large atypical lymphoid cells. Immunohistochemical staining was positive for CD10, CD20, BCL6, and MYC. The patient was diagnosed with DLBCL, Not Otherwise Specified (Germinal Center B-cell phenotype) and has started treatment. Discussion: This case demonstrates the importance of evaluating for underlying etiologies in cases with refractory or atypical presentations PUD.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Diagnosis and treatment of tuberculosis
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