# Yellow Nail Syndrome Presenting With a Complete Clinical Triad: A Report of a Rare Case

**Authors:** Md Shamsuzzaman, Kazi Azad, Mubina Ahmed, Ekramul Mustafa

PMC · DOI: 10.7759/cureus.100801 · Cureus · 2026-01-05

## TL;DR

A rare case of yellow nail syndrome with all three classic symptoms is reported, emphasizing the need for clinical awareness in older adults with unexplained lung fluid.

## Contribution

Presentation of a rare case with the complete triad of yellow nail syndrome, aiding in clinical recognition and management.

## Key findings

- A 76-year-old male exhibited all three features of yellow nail syndrome: yellow nails, lymphoedema, and pleural effusions.
- Timely diagnosis led to interventions like pleural catheter placement and talc pleurodesis, improving symptoms.
- The case underscores the importance of recognizing yellow nail syndrome in unexplained pleural effusions in older adults.

## Abstract

Yellow nail syndrome (YNS) is a rare disorder characterised by a triad of yellow nail discoloration, lymphoedema, and respiratory manifestations, including recurrent pleural effusions. A few hundred cases have been reported worldwide. Diagnosis is primarily clinical, as no definitive biomarkers exist, and the complete triad is seen in only a minority of patients. We report a 76-year-old male who presented with recurrent pleural effusions, non-pitting lower-limb oedema, and characteristic nail changes. Timely recognition of the classical triad allowed appropriate intervention, including indwelling pleural catheter placement and talc pleurodesis, leading to symptomatic improvement. This case highlights the importance of clinical vigilance in evaluating unexplained pleural effusions in older adults.

## Linked entities

- **Diseases:** Yellow nail syndrome (MONDO:0007921)

## Full-text entities

- **Diseases:** lower-limb oedema (MESH:D038061), nail discoloration (MESH:D014075), pleural effusions (MESH:D010996), YNS (MESH:D056684)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12869345/full.md

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Source: https://tomesphere.com/paper/PMC12869345