Three Years of Idiopathic Chylous Ascites: Splenic Marginal Zone Lymphoma Behind the Mask

Chylous ascites is rare in adults and is most commonly caused by lymphatic obstruction due to non-Hodgkin B-cell lymphoma. Splenic marginal zone lymphoma (SMZL) is an uncommon etiology. We report the case of an 89-year-old man with a three-year history of refractory chylous ascites initially considered of unknown origin. Clinical examination revealed significant ascites and splenomegaly. PET imaging demonstrated hypermetabolic lymphadenopathy, and bone marrow biopsy revealed infiltration by a CD5-/CD10- B-cell lymphoma consistent with SMZL. Analysis of ascitic fluid showed a predominance of T lymphocytes without a detectable B-cell clone. This case illustrates that SMZL, although rare, should be included in the differential diagnosis of persistent chylous ascites. A comprehensive diagnostic approach combining imaging, bone marrow biopsy, and flow cytometry is essential to establish a timely diagnosis and guide appropriate management, especially in elderly patients.

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Publication Details

Journal
Cureus
Published
2026-01-13
DOI
https://doi.org/10.7759/cureus.101496
Primary Topic
Lymphatic Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Three Years of Idiopathic Chylous Ascites: Splenic Marginal Zone Lymphoma Behind the Mask

Ismail Meziane, Catherine Letrillard, Mostefa Koroghli, Scholastique Ngo Souck M et al.
Cureus
Lymphatic Disorders and Treatments
article

Three Years of Idiopathic Chylous Ascites: Splenic Marginal Zone Lymphoma Behind the Mask

Ismail Meziane, Catherine Letrillard, Mostefa Koroghli, Scholastique Ngo Souck M, Rova Malala Fandresena Randrianarisoa
article en

Abstract

Chylous ascites is rare in adults and is most commonly caused by lymphatic obstruction due to non-Hodgkin B-cell lymphoma. Splenic marginal zone lymphoma (SMZL) is an uncommon etiology. We report the case of an 89-year-old man with a three-year history of refractory chylous ascites initially considered of unknown origin. Clinical examination revealed significant ascites and splenomegaly. PET imaging demonstrated hypermetabolic lymphadenopathy, and bone marrow biopsy revealed infiltration by a CD5-/CD10- B-cell lymphoma consistent with SMZL. Analysis of ascitic fluid showed a predominance of T lymphocytes without a detectable B-cell clone. This case illustrates that SMZL, although rare, should be included in the differential diagnosis of persistent chylous ascites. A comprehensive diagnostic approach combining imaging, bone marrow biopsy, and flow cytometry is essential to establish a timely diagnosis and guide appropriate management, especially in elderly patients.

CureusVol. 18(1)
Institution de Lavigny (CH), Universitäts Frauenklinik (DE)
Good health and well-being
Openalex Percentile: Top 89%
Lymphatic Disorders and Treatments
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