# Monoclonal Gammopathy of Neurological Significance in a Patient With Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS Syndrome): A Case Report of a Rare Entity

**Authors:** Andres E Prieto-Torres, Angela S Esparza-Albornoz, Nohora A Ovalle-Roa, Ivan Pisciotti-Chajin, Humberto Martinez-Cordero

PMC · DOI: 10.7759/cureus.67386 · Cureus · 2024-08-21

## TL;DR

A 71-year-old woman with CLIPPERS syndrome and a rare coexisting monoclonal gammopathy showed partial improvement with steroids but developed osteoporosis.

## Contribution

This case report highlights the rare coexistence of CLIPPERS syndrome and monoclonal gammopathy with neurological implications.

## Key findings

- The patient showed partial improvement with corticosteroid treatment for CLIPPERS syndrome.
- A monoclonal IgM peak was detected after ruling out common causes of peripheral neuropathy.
- Prolonged steroid use led to osteoporosis and fragility fractures, limiting mobility again.

## Abstract

Paraproteinemias or monoclonal gammopathies constitute a broad spectrum of heterogeneous clonal disorders of plasma cells characterized by the secretion of monoclonal proteins of heavy or light chains and the development of symptoms associated with them through mechanisms independent of tumor burden. Specifically, peripheral neuropathies represent an increasingly recognized manifestation of these paraproteinemias.

We report a case of a 71-year-old female who presented to the emergency department with clinical symptoms of perioral paresthesias associated with an ataxic gait that progressively compromised her functionality, eventually completely limiting her ability to walk. Initially diagnosed with chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS syndrome), management with corticosteroids was initiated, leading to partial improvement. After comprehensive etiological studies ruled out common causes of peripheral neuropathy (PN), a monoclonal peak of immunoglobulin M (IgM) was detected. With the initiation of appropriate treatment, the patient progressively regained her ability to walk. Unfortunately, due to prolonged corticosteroid use, she developed osteoporosis and multiple fragility fractures, which again limited her mobility. CLIPPERS syndrome coexisting with monoclonal gammopathy is extremely rare, highlighting the importance of this report.

## Linked entities

- **Proteins:** CD40LG (CD40 ligand)
- **Diseases:** osteoporosis (MONDO:0005298), peripheral neuropathy (MONDO:0003620)

## Full-text entities

- **Diseases:** tumor (MESH:D009369), CLIPPERS Syndrome (MESH:D013577), clonal disorders (MESH:C580365), perioral paresthesias (MESH:D010292), Gammopathy of Neurological Significance (MESH:D008998), Chronic Lymphocytic Inflammation (MESH:D015451), ataxic gait (MESH:D020234), fragility fractures (MESH:D005600), osteoporosis (MESH:D010024), PN (MESH:D010523), Paraproteinemias (MESH:D010265)
- **Chemicals:** Steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11414138/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11414138/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC11414138/full.md

---
Source: https://tomesphere.com/paper/PMC11414138