# An Adolescent Case of Anti-MDA5 Antibody-Positive Juvenile Dermatomyositis With Interstitial Lung Disease Successfully Treated by Multitarget Therapy Avoiding Cyclophosphamide: A Case Report and Literature Review

**Authors:** Tadafumi Yokoyama, Natsumi Inoue, Naoto Sakumura, Yuko Tasaki, Taizo Wada

PMC · DOI: 10.7759/cureus.62425 · Cureus · 2024-06-15

## TL;DR

A 13-year-old girl with a rare and severe form of juvenile dermatomyositis was successfully treated with a drug combination that avoided a harmful medication, preserving her fertility.

## Contribution

This case report demonstrates the effectiveness of multitarget therapy in treating anti-MDA5 antibody-positive JDM without using cyclophosphamide.

## Key findings

- The patient's ILD and skin symptoms improved with multitarget therapy.
- The patient remained in remission for three years without cyclophosphamide.
- Multitarget therapy is a promising alternative for preserving fertility in adolescent patients.

## Abstract

Juvenile dermatomyositis (JDM) patients who test positive for the antimelanoma differentiation-associated gene 5 (MDA5) antibody have a poor prognosis because of rapidly progressing interstitial lung disease (ILD). However, agreement on the best treatment for this condition remains elusive. We encountered a 13-year-old girl with anti-MDA5 antibody-positive JDM who presented with arthritis and was already showing signs of ILD when she was admitted to the hospital. While cyclophosphamide (CY) is commonly used, it can cause gonadal disorders and other complications when administered to adolescent females. Consequently, we chose multitarget therapy, which includes tacrolimus and mycophenolate mofetil. Her ILD and skin symptoms gradually improved, and she was able to maintain remission and avoid CY administration for three years. We conducted a thorough literature review to determine the efficacy and safety of multitarget therapy for anti-MDA5 antibody-positive DM and JDM. Multitarget therapy shows promise as a potentially effective and relatively safe treatment. The ability to avoid CY, which is especially important for adolescent patients concerned about fertility preservation, highlights a significant benefit of this multitarget therapy for anti-MDA5 antibody-positive DM and JDM patients.

## Linked entities

- **Proteins:** IFIH1 (interferon induced with helicase C domain 1)
- **Chemicals:** cyclophosphamide (PubChem CID 2907), tacrolimus (PubChem CID 445643), mycophenolate mofetil (PubChem CID 5281078)
- **Diseases:** juvenile dermatomyositis (MONDO:0008054), interstitial lung disease (MONDO:0015925)

## Full-text entities

- **Genes:** IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}
- **Diseases:** JDM (MESH:D003882), arthritis (MESH:D001168), DM (MESH:D009223), ILD (MESH:D017563), gonadal disorders (MESH:D006058)
- **Chemicals:** CY (MESH:D003520), mycophenolate mofetil (MESH:D009173), tacrolimus (MESH:D016559)
- **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/PMC11249054/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11249054/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC11249054/full.md

---
Source: https://tomesphere.com/paper/PMC11249054