# When Copper Meets Autoimmunity: A Rare Coexistence of Wilson's Disease and Systemic Lupus Erythematosus

**Authors:** Suresh Bhagoowani, Uooja Devi, Aqsa Munir, Ummulkiram Hasnain, Saad Khan, Javed Iqbal, Tehseen Akhtar

PMC · DOI: 10.1002/ccr3.70159 · Clinical Case Reports · 2025-02-19

## TL;DR

A rare case of Wilson's disease and lupus in a 17-year-old highlights the diagnostic challenges and severe complications from overlapping symptoms.

## Contribution

This case report highlights the rare coexistence of Wilson's disease and systemic lupus erythematosus and emphasizes the need for early diagnosis.

## Key findings

- The patient exhibited overlapping symptoms of Wilson's disease and systemic lupus erythematosus, leading to diagnostic challenges.
- Despite treatment, the patient's condition worsened due to complications from a blood transfusion reaction.
- Early recognition of Wilson's disease symptoms is critical to prevent severe outcomes in coexisting autoimmune conditions.

## Abstract

The coexistence of systemic lupus erythematosus (SLE) and Wilson's disease (WD) is exceedingly rare, posing significant diagnostic challenges due to overlapping clinical presentations. Neurological and psychiatric manifestations commonly associated with WD can obscure or mimic symptoms of other systemic diseases, complicating accurate diagnosis and management. We report the case of a 17‐year‐old female diagnosed with WD and concurrent SLE, treated at Civil Hospital, Karachi, Pakistan. The patient initially presented with neuropsychiatric symptoms typical of WD, confirmed by diagnostic findings indicative of hepatic copper accumulation. She later developed significant proteinuria, hematuria, fever, and positive autoimmune serologies, raising suspicion of concurrent SLE. Despite therapeutic interventions, including methylprednisolone (1 mg), the patient's condition deteriorated, and she unfortunately succumbed to complications from a blood transfusion reaction. This case underscores the importance of heightened clinical vigilance when managing overlapping presentations of WD and systemic autoimmune disorders like SLE. Early recognition of WD‐specific neurological and psychiatric symptoms is critical for timely diagnosis and intervention, potentially mitigating the risk of severe complications and poor outcomes.

## Linked entities

- **Diseases:** systemic lupus erythematosus (MONDO:0007915), Wilson's disease (MONDO:0010200)

## Full-text entities

- **Diseases:** hematuria (MESH:D006417), SLE (MESH:D008180), fever (MESH:D005334), neurological and psychiatric symptoms (MESH:D001523), hepatic copper accumulation (MESH:C535468), proteinuria (MESH:D011507), systemic autoimmune disorders (MESH:D020274), systemic diseases (MESH:D034721), WD (MESH:D006527)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11839759/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC11839759/full.md

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Source: https://tomesphere.com/paper/PMC11839759