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DOI: 10.1055/s-0034-1392874
Primary small-bowel diffuse large B-cell lymphoma presenting as hematemesis
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Publication History
Publication Date:
03 November 2015 (online)
A 32-year-old man with a past medical history of gastroesophageal reflux disease and gastric ulcers presented to the emergency department with hematemesis. He endorsed epigastric pain, one melanotic bowel movement, dizziness, and weakness. He denied previous episodes, aspirin or nonsteroidal anti-inflammatory drug use, and alcohol consumption.
On examination, the patient had hypotension and tachycardia, with epigastric tenderness in response to palpation and black stool on rectal examination. Laboratory test results indicated microcytic anemia, with a hemoglobin level of 8.0 g/dL that dropped to 6.2 g/dL after fluid resuscitation.
The patient was admitted to the intensive care unit, received blood products and intravenous esomeprazole, and underwent emergency esophagogastroduodenoscopy (EGD). This revealed blood in the gastric chamber and an ulcerated, oozing, circumferentially infiltrative mucosa in the second portion of the duodenum ([Fig. 1 a], [Fig.1 b], [Fig.1 c]). Abdominal computed tomography displayed localized thickening of the duodenal wall ([Fig. 2]).




During a second EGD, oozing from the lesion had ceased, so that tissue sampling was possible ([Fig. 1 d]). The histological and immunohistochemical findings were consistent with diffuse large B-cell lymphoma (DLBCL) ([Fig. 3 a], [Fig. 3 b], [Fig. 3 c], [Fig. 3 d], [Fig. 3 e], [Fig. 3 f]). Positron emission tomography (PET) revealed an area of increased metabolic activity in the second portion of the duodenum ([Fig. 4 a], [Fig. 4 b]).




The patient's treatment consisted of six cycles of chemotherapy with rituximab (Rituxan, Genentech and Biogen Idec), cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) given every 3 weeks. The patient tolerated the chemotherapy adequately, and interim PET after three cycles revealed a complete response to treatment ([Fig. 4 c], [Fig. 4 d]). The patient’s clinical course and imaging are summarized in [Video 1].
Clinical course and imaging of a patient with primary small-bowel diffuse large B-cell lymphoma presenting as hematemesisThe gastrointestinal tract is the most common site of extranodal non-Hodgkin lymphoma. However, isolated primary lesions of the duodenum are rare, accounting for fewer than 0.8 % of the cases [1]. The manifestations of gastrointestinal lymphoma vary with the subtype and anatomical location. For DLBCL, these frequently include weight loss, obstructive symptoms, abdominal pain, and lower gastrointestinal bleeding [2] [3]. This case is important in that it is the first well-documented case of intestinal DLBCL presenting with hematemesis.
Endoscopy_UCTN_Code_CCL_1AB_2AZ_3AB
Competing interests: None
Acknowledgments
We would like to thank Dr. Sarayu Chandrashekhar for her invaluable assistance in the pathologic interpretation of the tissue samples.
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References
- 1 Bautista-Quach MA, Ake CD, Chen M et al. Gastrointestinal lymphomas: morphology, immunophenotype and molecular features. J Gastrointest Oncol 2012; 3: 209-225
- 2 Koch P, del Valle F, Berdel WE et al. Primary gastrointestinal non-Hodgkin’s lymphoma: anatomic and histologic distribution, clinical features, and survival data of 371 patients registered in the German Multicenter Study GIT NHL 01/92. J Clin Oncol 2001; 19: 3861-3873
- 3 Ghimire P, Wu G-Y, Zhu L. Primary gastrointestinal lymphoma. World J Gastroenterol 2011; 17: 697-707
Corresponding author
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References
- 1 Bautista-Quach MA, Ake CD, Chen M et al. Gastrointestinal lymphomas: morphology, immunophenotype and molecular features. J Gastrointest Oncol 2012; 3: 209-225
- 2 Koch P, del Valle F, Berdel WE et al. Primary gastrointestinal non-Hodgkin’s lymphoma: anatomic and histologic distribution, clinical features, and survival data of 371 patients registered in the German Multicenter Study GIT NHL 01/92. J Clin Oncol 2001; 19: 3861-3873
- 3 Ghimire P, Wu G-Y, Zhu L. Primary gastrointestinal lymphoma. World J Gastroenterol 2011; 17: 697-707








