Evidence map›Paper›PMID 40502963›Full record

ArticleEuropean journal of case reports in internal medicine2025

Swollen Legs and False Nephrotic Syndrome: A Case of Primary Lymphatic Dysplasia with Intermittent Chyluria.

Giorgia Sasia, Teresa Morgillo, Christian Bracco, Corrado Magnino, Giulia Racca, Remo Melchio, Luigi Maria Fenoglio

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Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Giorgia SasiaDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Teresa MorgilloDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Christian BraccoDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Corrado MagninoDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Giulia RaccaDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Remo MelchioDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.
Luigi Maria FenoglioDepartment of Internal Medicine, Santa Croce and Carle General Hospital, Cuneo, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chyluria, defined as the presence of chyle in urine, is a rare condition caused by an abnormal communication between the lymphatic system and the urinary tract. It can present with massive proteinuria and characteristic milky urine, mimicking nephrotic syndrome. We report the case of a 23-year-old woman with a history of seronegative ocular myasthenia gravis who developed progressive bilateral lower extremity oedema and intermittent nephrotic-range proteinuria despite normal serum albumin and lipid profiles. A renal biopsy, performed to investigate proteinuria, was complicated by a subcapsular hematoma. Shortly thereafter, the patient developed dysuria, urinary retention, and milky urine, leading to the diagnosis of chyluria. Imaging revealed thrombosis of the left iliac vein, associated with hereditary thrombophilia (heterozygosity for factor V Leiden and homozygous LEARNING POINTS: Chyluria should be considered in patients presenting with milky urine and proteinuria, especially after excluding glomerular pathology.Non-parasitic causes, such as trauma or iatrogenic procedures like renal biopsy, are increasingly recognized in non-endemic regions.Conservative management, particularly dietary modifications with medium-chain triglycerides can lead to significant clinical improvement without invasive interventions.

Indexed as

Intermittent chylurialymphatic fistulanephrotic syndromevenous thrombosis

Identifiers

PMID40502963
PMCPMC12151559

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