# Anti-MDA5 Antibody-Positive Dermatomyositis-Associated Interstitial Lung Disease With a False-Positive Tuberculosis-Targeted RNA Capture (TB-TRC) Result: A Multimodal Management

**Authors:** Miho Shibata, Toyoshi Yanagihara, Makoto Fujimoto, Naoko Himuro, Kenji Ito, Naoki Hamada, Takato Ikeda, Kosuke Masutani, Masaki Fujita

PMC · DOI: 10.7759/cureus.87004 · Cureus · 2025-06-29

## TL;DR

A patient with a specific type of muscle disease and lung complications had a false test for tuberculosis, requiring careful treatment with multiple therapies.

## Contribution

This case highlights the importance of multimodal therapy and careful interpretation of false-positive TB-TRC results in anti-MDA5 RP-ILD.

## Key findings

- False-positive TB-TRC results can delay appropriate treatment in anti-MDA5 RP-ILD.
- Multimodal therapy including plasma exchange and JAK inhibition improved outcomes in refractory cases.
- Repeat testing confirmed the initial TB-TRC result was a false positive.

## Abstract

Anti-MDA5 antibody-positive dermatomyositis often causes rapidly progressive interstitial lung disease (RP-ILD) with high mortality. We present a 59-year-old man with three weeks of fever and dyspnea whose chest CT images showed bilateral subpleural ground-glass and reticular opacities. A markedly elevated anti-MDA5 titer and skin biopsy confirmed anti-MDA5 anti-positive dermatomyositis-associated RP-ILD. Tacrolimus plus nintedanib was initiated. Initial bronchoalveolar lavage fluid (BALF) testing on admission was unexpectedly positive for Mycobacterium tuberculosis by targeted RNA capture (TB-TRC), precluding cyclophosphamide and prompting plasma exchange, followed by intravenous immunoglobulin (IVIG). Repeat BALF TB-TRC and all sputum cultures remained negative for M. tuberculosis, confirming a false-positive result. On day 28, tofacitinib replaced tacrolimus due to persistent hyperferritinemia. The patient was discharged without home oxygen therapy on day 54. This case highlights the importance of interpreting rapid assays in context and using multimodal therapy - steroids, calcineurin inhibition, antifibrotics, plasma exchange, IVIG, and Janus kinase (JAK) inhibition - for refractory anti-MDA5 RP-ILD.

## Linked entities

- **Proteins:** IFIH1 (interferon induced with helicase C domain 1)
- **Chemicals:** tacrolimus (PubChem CID 445643), nintedanib (PubChem CID 135423438), tofacitinib (PubChem CID 9926791)
- **Diseases:** dermatomyositis (MONDO:0016367), interstitial lung disease (MONDO:0015925), tuberculosis (MONDO:0018076)

## Full-text entities

- **Genes:** IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, RIEG2 (Rieger syndrome 2) [NCBI Gene 6012] {aka ARS, RGS2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** muscle weakness (MESH:D018908), infectious (MESH:D003141), infection (MESH:D007239), malignancy (MESH:D009369), cytomegalovirus (MESH:D003586), opportunistic infections (MESH:D009894), hyperferritinemia (MESH:D000085583), inflammation (MESH:D007249), arthralgia (MESH:D018771), fever (MESH:D005334), Interstitial Lung Disease (MESH:D017563), papule (MESH:D000169), autoimmune emergencies (MESH:D004630), amyopathic dermatomyositis (MESH:C538250), rash (MESH:D005076), myalgia (MESH:D063806), bacterial pneumonia (MESH:D018410), lung injury (MESH:D055370), TB (MESH:D014390), Tuberculosis (MESH:D014376), dyspnea (MESH:D004417), hypogammaglobulinemia (MESH:D000361), hemorrhages (MESH:D006470), hypoxemia (MESH:D000860), influenza (MESH:D007251), critically ill (MESH:D016638), muscle involvement (MESH:C566343), bacterial infection (MESH:D001424), hypertension (MESH:D006973), fatigue (MESH:D005221), sore throat (MESH:D010612), cell suppression (MESH:D002292), lymphadenopathy (MESH:D008206), autoimmune disease (MESH:D001327), Dermatomyositis (MESH:D003882)
- **Chemicals:** TAC (MESH:D016559), steroids (MESH:D013256), NID (MESH:C530716), mPSL (MESH:D008775), cyclophosphamide (MESH:D003520), TOF (MESH:C479163), amlodipine (MESH:D017311), IVCY (-), minocycline (MESH:D008911), oxygen (MESH:D010100), garenoxacin (MESH:C419689)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mycoplasma (genus) [taxon 2093], Homo sapiens (human, species) [taxon 9606], Adenoviridae (family) [taxon 10508], Mycobacterium tuberculosis (species) [taxon 1773]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12308046/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12308046/full.md

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Source: https://tomesphere.com/paper/PMC12308046