S6007 The Hidden Culprit: Duodenal Lipoma Presenting as Chronic Abdominal Pain in a Young Adult

Introduction: Intestinal lipomas are uncommon benign tumors with an unknown etiology and an estimated incidence between 0.15% and 4.4%. Large lipomas can lead to complications such as intussusception or obstruction. We present a rare case of a young man with non-specific abdominal complaints found to have intestinal intussusception secondary to a duodenal lipoma. Case Description/Methods: A 34-year-old man with class 3 obesity presented with 7 months of worsening postprandial abdominal pain and fullness. He reported a 10-pound unintentional weight loss over 2 months and denied overt gastrointestinal bleeding. Exam revealed pale conjunctiva and a soft, non-tender abdomen. Laboratory workup was notable for microcytic anemia: hemoglobin 4.4 g/dL, MCV 68 fL, and ferritin 4 ng/mL. Complete metabolic panel including liver tests was unremarkable. He received 4 units of packed red blood cells with improvement in anemia. Computed tomography abdomen/pelvis showed a 10 cm lipomatous mass in the descending duodenum with upstream intussusception. Upper endoscopy revealed a duodenal mass originating in the bulb, causing intussusception. Superficial biopsies showed polypoid duodenal mucosa with foveolar metaplasia, ulceration/erosion, and granulation tissue. Tumor markers (CA 19-9, CEA, Chromogranin A) were normal. His hemoglobin remained stable and abdominal pain improved. Surgery team planned for outpatient lipoma resection, however he was lost to follow-up. Discussion: Duodenal lipomas are rare and can present with vague and non-specific gastrointestinal symptoms, which can lead to delayed diagnosis until complications occur. A literature review of 59 reported cases noted that 39% of duodenal lipomas arose in the second portion of the duodenum, with peak incidence typically between the fifth and seventh decades of life. Diagnosis is often established via radiologic imaging, commonly detected incidentally during computed tomography scans performed for non-specific abdominal complaints. Importantly, the mucosal surface of a lipoma may exhibit areas of ulceration or erosion that can cause anemia. Large symptomatic lipomas are treated with surgical or endoscopic resection, with endoscopic submucosal dissection. This case highlights the need to consider duodenal lipomas in small bowel intussusception and to recognize when surgical or endoscopic intervention is warranted to prevent future recurrences.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001152488.51863.31
Primary Topic
Gastrointestinal disorders and treatments
Type
article
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article

S6007 The Hidden Culprit: Duodenal Lipoma Presenting as Chronic Abdominal Pain in a Young Adult

Sunil Dacha, Scott Berger, Neal K. Bhachawat, Neha Mathur
The American Journal of Gastroenterology
Gastrointestinal disorders and treatments
article

S6007 The Hidden Culprit: Duodenal Lipoma Presenting as Chronic Abdominal Pain in a Young Adult

Sunil Dacha, Scott Berger, Neal K. Bhachawat, Neha Mathur
article en

Abstract

Introduction: Intestinal lipomas are uncommon benign tumors with an unknown etiology and an estimated incidence between 0.15% and 4.4%. Large lipomas can lead to complications such as intussusception or obstruction. We present a rare case of a young man with non-specific abdominal complaints found to have intestinal intussusception secondary to a duodenal lipoma. Case Description/Methods: A 34-year-old man with class 3 obesity presented with 7 months of worsening postprandial abdominal pain and fullness. He reported a 10-pound unintentional weight loss over 2 months and denied overt gastrointestinal bleeding. Exam revealed pale conjunctiva and a soft, non-tender abdomen. Laboratory workup was notable for microcytic anemia: hemoglobin 4.4 g/dL, MCV 68 fL, and ferritin 4 ng/mL. Complete metabolic panel including liver tests was unremarkable. He received 4 units of packed red blood cells with improvement in anemia. Computed tomography abdomen/pelvis showed a 10 cm lipomatous mass in the descending duodenum with upstream intussusception. Upper endoscopy revealed a duodenal mass originating in the bulb, causing intussusception. Superficial biopsies showed polypoid duodenal mucosa with foveolar metaplasia, ulceration/erosion, and granulation tissue. Tumor markers (CA 19-9, CEA, Chromogranin A) were normal. His hemoglobin remained stable and abdominal pain improved. Surgery team planned for outpatient lipoma resection, however he was lost to follow-up. Discussion: Duodenal lipomas are rare and can present with vague and non-specific gastrointestinal symptoms, which can lead to delayed diagnosis until complications occur. A literature review of 59 reported cases noted that 39% of duodenal lipomas arose in the second portion of the duodenum, with peak incidence typically between the fifth and seventh decades of life. Diagnosis is often established via radiologic imaging, commonly detected incidentally during computed tomography scans performed for non-specific abdominal complaints. Importantly, the mucosal surface of a lipoma may exhibit areas of ulceration or erosion that can cause anemia. Large symptomatic lipomas are treated with surgical or endoscopic resection, with endoscopic submucosal dissection. This case highlights the need to consider duodenal lipomas in small bowel intussusception and to recognize when surgical or endoscopic intervention is warranted to prevent future recurrences.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Gastrointestinal disorders and treatments
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