# Diffuse Cutaneous Systemic Sclerosis With Normotensive Scleroderma Renal Crisis and Myopericarditis: A Case Report

**Authors:** Luís Augusto Barbosa Franco Zörrer, Lucas Yugi de Souza Terui, Rodrigo Fanini Balena, Ana Luisa Woidello Miyazima, Rafael Miyazima

PMC · DOI: 10.7759/cureus.78858 · Cureus · 2025-02-11

## TL;DR

This case report describes a rare and severe case of systemic sclerosis with normotensive kidney crisis and heart inflammation, highlighting the challenges in diagnosis and treatment.

## Contribution

The paper presents a rare clinical case of normotensive scleroderma renal crisis with myopericarditis in a patient with diffuse cutaneous systemic sclerosis.

## Key findings

- Normotensive scleroderma renal crisis can present without hypertension, making it harder to diagnose.
- Cardiac complications like myopericarditis worsen the prognosis and complicate treatment.
- Early recognition and management of normotensive renal crisis are crucial for better outcomes.

## Abstract

Systemic sclerosis (SSc) is a rare autoimmune disease characterized by fibrosis and multi-organ dysfunction, primarily affecting the heart, lungs, and kidneys. Scleroderma renal crisis (SRC) can present as hypertensive or normotensive, with the latter being more challenging to diagnose due to the absence of hypertension at onset. Normotensive SRC carries a worse prognosis, with an increased risk of renal failure and a poor response to treatment. The presence of cardiac complications, such as myopericarditis, further exacerbates the clinical course, creating significant management challenges. Moreover, hypotension in normotensive SRC complicates therapeutic interventions, particularly the use of angiotensin-converting enzyme (ACE) inhibitors.

This case report highlights a patient with diffuse cutaneous systemic sclerosis (dcSSc) who presented with normotensive SRC complicated by myopericarditis, resulting in acute renal and heart failure. It underscores the need for early recognition of this rare form of renal crisis, especially when accompanied by cardiac complications, given its atypical presentation without significant hypertension at onset. The report emphasizes the critical importance of identifying risk factors and addressing the challenges of managing normotensive SRC to improve patient outcomes.

## Linked entities

- **Diseases:** systemic sclerosis (MONDO:0005100), renal failure (MONDO:0001106)

## Full-text entities

- **Diseases:** SRC (MESH:D012595), renal failure (MESH:D051437), multi-organ dysfunction (MESH:D009102), autoimmune disease (MESH:D001327), Myopericarditis (MESH:D010146), hypotension (MESH:D007022), cardiac complications (MESH:D006331), Diffuse Cutaneous Systemic Sclerosis (MESH:D045743), fibrosis (MESH:D005355), renal crisis (MESH:D006030), acute renal and heart failure (MESH:D058186), hypertension (MESH:D006973)
- **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/PMC11906016/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC11906016/full.md

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Source: https://tomesphere.com/paper/PMC11906016