# Silent Storm Unveiled: Lupus Nephritis and Cerebral Vasculitis in Systemic Lupus Erythematosus

**Authors:** Rucha Sawant, Shilpa A Gaidhane, Vrushali Mahajan, Pranav Chaudhari, Gautam N Bedi

PMC · DOI: 10.7759/cureus.57751 · Cureus · 2024-04-07

## TL;DR

This paper presents a case of systemic lupus erythematosus complicated by cerebral vasculitis and lupus nephritis, highlighting the challenges in diagnosing complex autoimmune disorders.

## Contribution

The paper contributes a detailed case study linking SLE with concurrent cerebral vasculitis and lupus nephritis, emphasizing diagnostic challenges.

## Key findings

- A patient presented with seizures, rash, ulcers, and fever, later diagnosed with SLE, cerebral vasculitis, and lupus nephritis.
- Diagnosis required integrating clinical symptoms, lab tests, neuroimaging, and renal biopsy.
- Early detection of CNS and renal involvement in SLE remains challenging due to nonspecific symptoms.

## Abstract

Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder known for its intricate clinical manifestations, spanning a spectrum of symptoms, including neuropsychiatric SLE (NPSLE) and lupus nephritis (LN). This condition predominantly affects young women of childbearing age, presenting a diverse array of symptoms that pose challenges in both diagnosis and treatment. Diagnosing central nervous system (CNS) involvement in SLE remains notably difficult despite being rooted in an autoimmune inflammatory response driven by cytokine surges. There exists no single definitive test for diagnosis, necessitating a thorough evaluation of clinical presentations, neurological indicators, and specific antibody detection. LN typically evades diagnosis until the patient progresses to a state of advanced renal insufficiency, demanding aggressive therapeutic interventions. In this discourse, we examine a case marked by generalized tonic-clonic seizures. While epilepsy might be initially suspected, in this instance, the underlying cause lay deeper, concealed within the complexities of autoimmune dysregulation. Additional symptoms included generalized edema, sun-exposed rash, oral ulcers, and recurrent fever over the past six months. The puzzle pieces eventually coalesced through meticulous examination of each clinical manifestation, coupled with laboratory analyses, neuroimaging studies, and renal biopsy, revealing a complex scenario of cerebral vasculitis concurrent with LN in a case of SLE.

## Linked entities

- **Diseases:** Systemic Lupus Erythematosus (MONDO:0007915), lupus nephritis (MONDO:0005556), epilepsy (MONDO:0005027)

## Full-text entities

- **Diseases:** renal insufficiency (MESH:D051437), fever (MESH:D005334), NPSLE (MESH:D020945), autoimmune inflammatory (MESH:D007249), epilepsy (MESH:D004827), tonic-clonic seizures (MESH:D012640), autoimmune disorder (MESH:D001327), rash (MESH:D005076), LN (MESH:D008181), SLE (MESH:D008180), edema (MESH:D004487), oral ulcers (MESH:D019226), autoimmune dysregulation (MESH:C580192), central nervous system (CNS) involvement (MESH:C538190), Cerebral Vasculitis (MESH:D020293)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11074806/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC11074806/full.md

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Source: https://tomesphere.com/paper/PMC11074806