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Case Reports
. 2021 Mar 18;15(1):379-388.
doi: 10.1159/000513972. eCollection 2021 Jan-Apr.

Collision Tumor Comprising Primary Malignant Lymphoma and Adenocarcinoma in the Ascending Colon

Affiliations
Case Reports

Collision Tumor Comprising Primary Malignant Lymphoma and Adenocarcinoma in the Ascending Colon

Jun Kataoka et al. Case Rep Gastroenterol. .

Abstract

We describe the case of a 78-year-old man with collision tumor from the primary malignant lymphoma and adenocarcinoma in the ascending colon. He suffered anemia from sigmoid colon cancer, and colonoscopy revealed early-stage colorectal cancer with a diameter of 20 mm in the cecum, the biopsy specimen showed moderately differentiated adenocarcinoma. Contrast-enhanced computed tomography (CT) revealed bowel wall thickening with contrast enhancement at the cecum; however, no lymph node and organ metastases were found. As above, we performed laparoscopic ileocecal resection with D3 lymph node dissection. The postoperative course was uneventful, and he was discharged from the hospital on postoperative day 11. Histopathological findings were moderately differentiated adenocarcinoma which invaded the muscularis propria and serosa from the submucosa, while the adjacent serosa showed a highly diffuse proliferation of atypical cells with an irregular nuclear-to-cytoplasmic ratio. Besides, immunohistochemical staining findings were diffuse large B-cell lymphoma, and diffuse large B-cell lymphoma was coexistent with moderately differentiated adenocarcinoma. We treated the patient with cyclophosphamide, doxorubicin, vincristine, and prednisolone in combination with rituximab (R-CHOP therapy) during 3 months postoperatively. When the 8 courses had been completed, postoperative positron emission tomography-CT (PET-CT) confirmed complete response, and the disease control has been doing well. Malignant lymphoma of the colorectal region is relative rare, and the occurrence of synchronous lymphoma and adenocarcinoma of the colon is also rare. Furthermore, collision tumor by these different entities is very unusual. We presented here such a case. The accurate clinical determination of the dominant tumor and a close follow-up is required for proper treatment in these cases.

Keywords: Adenocarcinoma; Collision tumor; Diffuse large B-cell lymphoma; Ileocecal region.

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Conflict of interest statement

The authors have no conflicts of interest to disclose.

Figures

Fig. 1
Fig. 1
Preoperative total colonoscopy. a, b Total colonoscopy detected a 20-mm-sized ulcerative mass in the ascending colon (black arrow), and a biopsy specimen from the mass revealed a moderately differentiated adenocarcinoma of the colon.
Fig. 2
Fig. 2
Macroscopic findings. The specimen showed a long ulcerative mass with a diameter of 18 mm, a moderately differentiated adenocarcinoma of the colon which invaded the muscularis propria and serosa from the submucosa.
Fig. 3
Fig. 3
Microscopic, morphological, and immunohistochemical findings. a A photograph of the specimen (hematoxylin and eosin [H&E] staining, original magnification 40×) shows evidence of a colliding lymphoma (lower) and moderately differentiated adenocarcinoma (upper). b H&E-stain of moderately differentiated adenocarcinoma that invaded the muscularis propria and serosa from the submucosa (original magnification 100×). c H&E-stain of highly diffused proliferation of atypical cells with irregular nuclear-to-cytoplasmic ratio was observed in the adjacent serosa (original magnification 100×); and cytoplasmic immunohistochemical positivity for B-cell marker cluster of differentiation 20 through; d immunochemical staining 20×, and e immunochemical staining 40×, for cluster of differentiation (CD) 20; f immunochemical staining 20×, and g immunochemical staining 40×, for CD79α; h immunochemical staining 20×, and i immunochemical staining 40×, for CD 3; j immunochemical staining 20×, and k immunochemical staining 40×, for B-cell lymphoma (Bcl)-2; l immunochemical staining 20×, and m immunochemical staining 40×, for Bcl-6; n immunochemical staining 20×, and o immunochemical staining 40×, for Epstein Barr virus nuclear antigen2.

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