Endoscopy 2014; 46(S 01): E126-E127
DOI: 10.1055/s-0034-1364941
Cases and Techniques Library (CTL)
© Georg Thieme Verlag KG Stuttgart · New York

Mantle cell lymphoma of the colon

Authors

  • Mohammad Esmadi

    Department of Internal Medicine, University of Missouri School of Medicine, Columbia, Missouri, USA
  • Dina S. Ahmad

    Department of Internal Medicine, University of Missouri School of Medicine, Columbia, Missouri, USA
  • Deiter J. Duff

    Department of Internal Medicine, University of Missouri School of Medicine, Columbia, Missouri, USA
  • Hazem T. Hammad

    Department of Internal Medicine, University of Missouri School of Medicine, Columbia, Missouri, USA
Further Information

Corresponding author

Mohammad Esmadi, MD
One Hospital Dr.
DC043.00 Health Sciences Center
Columbia
MO 65212
USA   
Fax: +1-573-884-5690   

Publication History

Publication Date:
27 March 2014 (online)

 

An 81-year-old man with a history of stage IV mantle cell lymphoma (MCL) diagnosed from a submental lymph node biopsy in 2006 was evaluated for new-onset melena and blood clots with bowel movements. He had been treated for his MCL with 6 cycles of CHOP-R (cyclophosphamide, doxorubicin, vincristine, prednisone, and rituximab) in 2006, followed by 13 cycles of maintenance rituximab. In 2012, he was started on lenalidomide (Revlimid), but decided to stop after an exacerbation of his heart failure.

On presentation, his hemoglobin was 5.2 g/dL. Colonoscopy showed a 4-cm mass in the cecal base ([Fig. 1]), a 5-cm ulcerated mass encircling the ileocecal valve, and six sessile odd-looking polypoid masses in the cecal base. Biopsy was consistent with MCL ([Fig. 2], [Fig. 3], [Fig. 4], [Fig. 5]). Because of the patient’s heart failure, surgical resection was not favored. He was started on radiotherapy and chlorambucil.

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Fig. 1 Colonoscopy picture showing a 4-cm mass in the cecal base with multiple polypoid masses.
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Fig. 2 a Low-power H&E-stained section shows a diffuse lymphoid infiltrate underlying colonic mucosa. Overall, the architecture was vaguely nodular. b Higher-power H&E-stained section shows a monotonous population of small- to intermediate-size lymphocytes with scant cytoplasm and irregular nuclear borders.
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Fig. 3 Immunohistochemical stain for PAX5 (a B-cell marker) is positive in tumor cells.
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Fig. 4 Immunohistochemical stain for CD20 (a B-cell marker) is positive in tumor cells.
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Fig. 5 Immunohistochemical stain for cyclin D1 is positive.

MCL is one of the mature B-cell non-Hodgkin lymphomas. Most patients with MCL present with advanced-stage disease, and up to 80 % have involvement of extranodal sites, including the spleen, bone marrow, and gastrointestinal tract. Gastrointestinal tract involvement was detected in 10 % – 28 % of MCL cases in various series [1] [2]. The typical appearance of intestinal MCL is multiple lymphomatous polyposis. Less commonly, it appears as protruded lesions or superficial lesions. MCL expresses pan-B-cell antigens, CD5, and FMC7. Cyclin D1 is helpful to distinguish MCL from other lymphomas.

Endoscopy_UCTN_Code_CCL_1AD_2AC


Competing interests: None


Corresponding author

Mohammad Esmadi, MD
One Hospital Dr.
DC043.00 Health Sciences Center
Columbia
MO 65212
USA   
Fax: +1-573-884-5690   


Zoom
Fig. 1 Colonoscopy picture showing a 4-cm mass in the cecal base with multiple polypoid masses.
Zoom
Fig. 2 a Low-power H&E-stained section shows a diffuse lymphoid infiltrate underlying colonic mucosa. Overall, the architecture was vaguely nodular. b Higher-power H&E-stained section shows a monotonous population of small- to intermediate-size lymphocytes with scant cytoplasm and irregular nuclear borders.
Zoom
Fig. 3 Immunohistochemical stain for PAX5 (a B-cell marker) is positive in tumor cells.
Zoom
Fig. 4 Immunohistochemical stain for CD20 (a B-cell marker) is positive in tumor cells.
Zoom
Fig. 5 Immunohistochemical stain for cyclin D1 is positive.