Endoscopy 2008; 40: E149
DOI: 10.1055/s-2007-995772
Unusual cases and technical notes

© Georg Thieme Verlag KG Stuttgart · New York

Chronic anemia masking a primary large B-cell lymphoma of the small intestine, finally diagnosed by double-balloon enteroscopy

K.  Weigand1 , T.  M.  Ganten1 , M.  Andrulis2 , W.  Stremmel1 , P.  Sauer1 , A.  Schaible3
  • 1Department of Gastroenterology and Hepatology, University Hospital Heidelberg, Germany
  • 2Department of Pathology, University Hospital Heidelberg, Germany
  • 3Department of General Surgery, University Hospital Heidelberg, Germany
Further Information

K. Weigand,MD 

Department of Gastroenterology and Hepatology

Medizin IV, University Hospital Heidelberg

Im Neuenheimer Feld 410

69120 Heidelberg

Germany

Email: kilian_weigand@med.uni-heidelberg.de

Publication History

Publication Date:
16 July 2008 (online)

Table of Contents

A 78-year-old woman was transferred to our hospital with a history of chronic anemia (hemoglobin 80 – 90 g/L) for several months that was refractory to iron treatment. Repeated gastroscopy and colonoscopy showed no abnormal findings. During the ensuing wireless capsule endoscopy, mucosal changes interpreted as ‘possibly ulcerations’ located within the distal part of the jejunum were identified as a possible source of bleeding. We performed double-balloon enteroscopy (DBE) to confirm these findings and carry out tissue sampling. Approximately 250 cm distal to the ligament of Treitz we identified a polypoid elevated mucosal lesion of inflamed appearance with erosions and flat ulcerations ([Fig. 1]). During further diagnostic evaluation using hydro-CT, a lymphoma of the small bowel (jejunum) was suggested ([Fig. 2]). In addition, many nonenlarged mesenteric and retroperitoneal lymph nodes were described. Histological analysis of the biopsies taken during DBE showed an intestinal B-cell lymphoma with diffuse large cells ([Fig. 3]). Any thoracic or mediastinal manifestation was excluded by CT scan. Bone marrow histology and cytology demonstrated normal findings with slightly enhanced erythropoiesis and no infiltration by lymphoma cells. Serology showed slight anemia and iron deficiency, as well as enhanced values for CD25 (6601 U/mL, normal < 900 U/mL), LDH (350 U/L, normal < 248 U/L) and β-microglobulin (4.9 mg/L, normal < 2.5 mg/L). A diagnosis of primary B-cell lymphoma of the small intestine was made.

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Fig. 1 a, b Endoscopy showing a suspect area approximately 250 cm distal to the ligament of Treitz.

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Fig. 2 Contrast-enhanced hydro-CT scan showing thickened wall of the jejunum and enlarged lymph nodes, suggestive of lymphoma infiltration.

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Fig. 3 Histological section of the mucosal area shown in Fig. 1, showing a diffuse large B-cell lymphoma. All proliferating cells are immunohistochemically stained using MiB-1. Original magnification × 20.

Small-bowel lymphomas are not typically associated with occult bleeding [1] [2]. The most commonly described symptoms are weight loss, diarrhea, obstruction, and abdominal pain [3] [4]. The case presented here supports the idea that capsule endoscopy and DBE may be considered as preferred procedures in evaluating chronic anemia that is suggestive of intestinal lymphoma.

Endoscopy_UCTN_Code_CCL_1AC_2AC

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References

  • 1 Daum S, Ullrich R, Heise W. et al . Intestinal non-Hodkin’s lymphoma: a multicenter prospective clinical study from the German Study Group on Intestinal non-Hodkin’s Lymphoma.  J Clin Oncol. 2003;  21 2740
  • 2 Hatzaras I, Palesty J A, Abir F. et al . Small-bowel tumors: epidemiologic and clinical characteristics of 1260 cases from the Connecticut tumor registry.  Arch Surg. 2007;  142 229-235
  • 3 Yin L, Chen C Q, Peng C H. et al . Primary small-bowel non-Hodgkin’s lymphoma: a study of clinical features, pathology, management and prognosis.  J Int Med Res. 2007;  35 406-415
  • 4 Al-Saleem T, Al-Mondhiry H. Immunoproliferative small intestinal disease (IPSID): a model for mature B-cell neoplasms.  Blood. 2005;  105 2274-2280

K. Weigand,MD 

Department of Gastroenterology and Hepatology

Medizin IV, University Hospital Heidelberg

Im Neuenheimer Feld 410

69120 Heidelberg

Germany

Email: kilian_weigand@med.uni-heidelberg.de

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References

  • 1 Daum S, Ullrich R, Heise W. et al . Intestinal non-Hodkin’s lymphoma: a multicenter prospective clinical study from the German Study Group on Intestinal non-Hodkin’s Lymphoma.  J Clin Oncol. 2003;  21 2740
  • 2 Hatzaras I, Palesty J A, Abir F. et al . Small-bowel tumors: epidemiologic and clinical characteristics of 1260 cases from the Connecticut tumor registry.  Arch Surg. 2007;  142 229-235
  • 3 Yin L, Chen C Q, Peng C H. et al . Primary small-bowel non-Hodgkin’s lymphoma: a study of clinical features, pathology, management and prognosis.  J Int Med Res. 2007;  35 406-415
  • 4 Al-Saleem T, Al-Mondhiry H. Immunoproliferative small intestinal disease (IPSID): a model for mature B-cell neoplasms.  Blood. 2005;  105 2274-2280

K. Weigand,MD 

Department of Gastroenterology and Hepatology

Medizin IV, University Hospital Heidelberg

Im Neuenheimer Feld 410

69120 Heidelberg

Germany

Email: kilian_weigand@med.uni-heidelberg.de

Zoom Image
Zoom Image

Fig. 1 a, b Endoscopy showing a suspect area approximately 250 cm distal to the ligament of Treitz.

Zoom Image

Fig. 2 Contrast-enhanced hydro-CT scan showing thickened wall of the jejunum and enlarged lymph nodes, suggestive of lymphoma infiltration.

Zoom Image

Fig. 3 Histological section of the mucosal area shown in Fig. 1, showing a diffuse large B-cell lymphoma. All proliferating cells are immunohistochemically stained using MiB-1. Original magnification × 20.