# Intermittent White Urine With Nephrotic-Range Proteinuria and Preserved Renal Function: A Diagnostic Dilemma Between Chyluria, Pseudochyluria, and Amyloidosis

**Authors:** Firdaus Jabeen, Vaibhav Shukla, Salil Vallecha, Monis Khan, Saboor Mateen

PMC · DOI: 10.7759/cureus.102810 · Cureus · 2026-02-02

## TL;DR

A woman with white urine and kidney issues had a difficult diagnosis between chyluria, pseudochyluria, and amyloidosis.

## Contribution

The case highlights diagnostic challenges in distinguishing chyluria from pseudochyluria and amyloidosis with limited tissue samples.

## Key findings

- The patient had nephrotic-range proteinuria with preserved kidney function and intermittent white urine.
- Tests for chyluria, tuberculosis, and amyloidosis were negative despite suggestive symptoms.
- The case illustrates diagnostic uncertainty when tissue samples are non-representative.

## Abstract

Milky or “white” urine is usually attributed to chyluria but may also result from lipid-rich proteinuric urine or crystals (“pseudochyluria”). We describe a 47-year-old woman with a 6-month history of intermittent white urine, bilateral edema, nephrotic-range proteinuria (20.3 g/24 h), preserved renal function, near-normal serum albumin, and chronic bronchiectasis. Evaluation for parasitic and non-parasitic chyluria, tuberculosis, and systemic amyloidosis was repeatedly negative. A fasting urine sample showed markedly raised triglycerides but negative tests for chyle. The kidney biopsy was non-representative, and the abdominal fat-pad biopsy was Congo-red-negative. Serum anti-PLA2R antibodies and free light chains were normal. The case illustrates the gray zone between chyluria and pseudochyluria and the challenge of defining the underlying glomerular lesion when tissue diagnosis is limited.

## Linked entities

- **Diseases:** amyloidosis (MONDO:0019065), tuberculosis (MONDO:0018076)

## Full-text entities

- **Genes:** CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, C1QA (complement C1q A chain) [NCBI Gene 712] {aka C1QD1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PLA2R1 (phospholipase A2 receptor 1) [NCBI Gene 22925] {aka CLEC13C, PLA2-R, PLA2G1R, PLA2IR, PLA2R}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** hematuria (MESH:D006417), filariasis (MESH:D005368), nephrotic (MESH:D009404), AA (MESH:C566236), Chronic bronchiectasis (MESH:D001987), inflammatory (MESH:D007249), chyle loss (MESH:D016388), urinary tract obstruction (MESH:D014552), weight loss (MESH:D015431), colicky pain (MESH:D015746), cystic fibrosis (MESH:D003550), leak (MESH:D019559), cough (MESH:D003371), allergic bronchopulmonary aspergillosis (MESH:D001229), edema (MESH:D004487), lymphatico-urinary fistula (MESH:D014548), systemic amyloidosis (MESH:D009101), filarial infection (MESH:D007239), minimal-change disease (MESH:D009402), post-infective bronchiectasis (MESH:D000094025), plasma cell dyscrasia (MESH:D010265), diabetes (MESH:D003920), renal amyloidosis (MESH:C538249), filarial chyluria (MESH:D004605), tuberculosis (MESH:D014376), AA amyloidosis (MESH:C000718787), secondary immunodeficiency (MESH:D000068376), lymphatic disease (MESH:D008206), AL amyloidosis (MESH:D000075363), membranous nephropathy (MESH:D015433), primary ciliary dyskinesia (MESH:D002925), Amyloidosis (MESH:D000686), glomerular lesion (MESH:D007674), dysuria (MESH:D053159), pyuria (MESH:D011776), tuberculous (MESH:D014390), HIV (MESH:D015658), primary immunodeficiency (MESH:D000081207), fistula (MESH:D005402), Nephrotic-Range Proteinuria (MESH:D011507), fever (MESH:D005334)
- **Chemicals:** QuantiFERON-TB Gold (-), telmisartan (MESH:D000077333), triglycerides (MESH:D014280), torsemide (MESH:D000077786), dapagliflozin (MESH:C529054), Congo red (MESH:D003224), C (MESH:D002244), lipid (MESH:D008055), dietary sodium (MESH:D012982), creatinine (MESH:D003404)
- **Species:** Candida [taxon 1535326], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12958002/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958002/full.md

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Source: https://tomesphere.com/paper/PMC12958002