Waldenström macroglobulinaemia presenting with suspected protein-losing enteropathy and nodular polypoidal duodenal mucosal changes: a case report

Gastrointestinal involvement in Waldenström macroglobulinaemia is uncommon, and presentation with features suggestive of protein-losing enteropathy and nodular polypoidal duodenal mucosa is particularly rare. A 67-year-old man presented with persistent, non-bloody diarrhoea, progressive anorexia, and significant weight loss for three years. Laboratory evaluation revealed profound hypoalbuminaemia and mild normocytic anaemia, with preserved hepatic and renal function. Extensive gastrointestinal investigations, including upper and lower endoscopies with biopsies, revealed nodular polypoidal duodenal abnormalities. Histopathological examination repeatedly showed intravascular fibrinoid material, which can occur in various vascular or inflammatory conditions, but did not establish a definitive diagnosis. Despite symptomatic management, his condition gradually worsened. Bone marrow aspiration and biopsy showed lymphoplasmacytic infiltration with an immunophenotype supporting lymphoplasmacytic lymphoma. Subsequent serum protein electrophoresis demonstrated a monoclonal protein, and the overall clinicopathological findings supported a diagnosis of lymphoplasmacytic lymphoma/Waldenström macroglobulinaemia. Treatment with dexamethasone, rituximab, and cyclophosphamide led to marked clinical and biochemical improvement, with resolution of diarrhoea and normalisation of serum albumin, suggesting an association between Waldenström macroglobulinaemia and the gastrointestinal manifestations. This case highlights an unusual gastrointestinal manifestation of Waldenström macroglobulinaemia presenting with chronic diarrhoea and severe hypoalbuminaemia suggestive of protein-losing enteropathy. When conventional gastrointestinal investigations are unrevealing, underlying haematological malignancies should be considered in the differential diagnosis of unexplained hypoalbuminaemia and chronic diarrhoea.

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Journal
BMC Gastroenterology
Published
2026-09-28
DOI
https://doi.org/10.1186/s12876-026-05392-2
Primary Topic
Celiac Disease Research and Management
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article
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article

Waldenström macroglobulinaemia presenting with suspected protein-losing enteropathy and nodular polypoidal duodenal mucosal changes: a case report

Chamara Sarathchandra, Sisira Hemananda Siribaddana, Umavi Halkewela, Chinthaka Viduranga De Silva et al.
BMC Gastroenterology
Celiac Disease Research and Management
article

Waldenström macroglobulinaemia presenting with suspected protein-losing enteropathy and nodular polypoidal duodenal mucosal changes: a case report

Chamara Sarathchandra, Sisira Hemananda Siribaddana, Umavi Halkewela, Chinthaka Viduranga De Silva, Amila Amarasena, Asanthi Jayanjana Nileththi
article en

Abstract

Gastrointestinal involvement in Waldenström macroglobulinaemia is uncommon, and presentation with features suggestive of protein-losing enteropathy and nodular polypoidal duodenal mucosa is particularly rare. A 67-year-old man presented with persistent, non-bloody diarrhoea, progressive anorexia, and significant weight loss for three years. Laboratory evaluation revealed profound hypoalbuminaemia and mild normocytic anaemia, with preserved hepatic and renal function. Extensive gastrointestinal investigations, including upper and lower endoscopies with biopsies, revealed nodular polypoidal duodenal abnormalities. Histopathological examination repeatedly showed intravascular fibrinoid material, which can occur in various vascular or inflammatory conditions, but did not establish a definitive diagnosis. Despite symptomatic management, his condition gradually worsened. Bone marrow aspiration and biopsy showed lymphoplasmacytic infiltration with an immunophenotype supporting lymphoplasmacytic lymphoma. Subsequent serum protein electrophoresis demonstrated a monoclonal protein, and the overall clinicopathological findings supported a diagnosis of lymphoplasmacytic lymphoma/Waldenström macroglobulinaemia. Treatment with dexamethasone, rituximab, and cyclophosphamide led to marked clinical and biochemical improvement, with resolution of diarrhoea and normalisation of serum albumin, suggesting an association between Waldenström macroglobulinaemia and the gastrointestinal manifestations. This case highlights an unusual gastrointestinal manifestation of Waldenström macroglobulinaemia presenting with chronic diarrhoea and severe hypoalbuminaemia suggestive of protein-losing enteropathy. When conventional gastrointestinal investigations are unrevealing, underlying haematological malignancies should be considered in the differential diagnosis of unexplained hypoalbuminaemia and chronic diarrhoea.

BMC Gastroenterology
Post Graduate Institute of Medicine, University of Colombo, Sri Lanka (LK), Rajarata University of Sri Lanka (LK), University of Colombo (LK)
Good health and well-being
Openalex Percentile: Top 10%
Celiac Disease Research and Management
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