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Table 2 Comparison on coexistent anti-aminoacyl-tRNA synthetase (anti-ARS)-interstitial lung disease (ILD) dermatomyositis with anti-melanoma differentiation-associated gene 5 (MDA5)-ILD dermatomyositis

From: Double anti-PL-7 and anti-MDA-5 positive Amyopathic Dermatomyositis with rapidly progressive interstitial lung disease in a Hispanic patient

 

Naniwa et al. [3]

Takecuchi et al. [4]

Current case

Patient ethnicity

Japanese

Japanese

Hispanic

Gender

Male

Female

Female

Age

70-year-old

53-year-old

27-year-old

Anti-ARS antibodies

Yes, anti-threonyl-transfer RNA synthetase (anti-PL-7)

Yes, Anti-glycyl-tRNA synthetase (anti-EJ)

Yes, anti-threonyl-transfer RNA synthetase (anti-PL-7)

Anti-MDA-5 antibodies

Yes

Yes

Yes

Diagnostic testing tool

Immunoprecipitation assay

Immunoprecipitation assay

Commercial Immunoblot assay

Skin manifestation

Facial rash, a V-sign rash, a periungual erythema, and nail fold bleeding

heliotrope rash, facial erythema, Gottron papules with some shallow ulcers, mechanic’s hands and periungual erythema

forme fruste of Gottron’s patches

Pulmonary Manifestation

Fine crackles were heard bilaterally in the lower lung field

Lung auscultation identified considerable fine crackles bilaterally

Diffuse crackles at lung auscultation bilaterally

Chest computed tomography findings

Not done

Initial presentation with anti-EJ only: lower peripheral reticulation and ground-glass attenuation (GGA)

15 years after onset during exacerbation with anti-MDA5 only:

rapidly progressive course with newly developed random GGA

Extensive ground glass opacities bilaterally without bronchiectasis