Dermatomyositis sine dermatitis-an unusual non classical dermatomyositis with amyopathic myopathy tale: a case report

We report a 13-year-old girl with dermatomyositis sine dermatitis (DMSD), a rare form of juvenile DM characterized by muscle weakness without skin rash. She presented with 2 months of progressive proximal limb weakness, neck weakness, and bilateral hand paresthesias, but no skin findings. Laboratory tests showed elevated inflammation with normal creatine kinase and significant hypokalemia. Myositis autoantibody testing revealed strongly positive anti-NXP2 and anti-Ku antibodies. A diagnosis of DMSD was made. High-dose corticosteroids plus supportive care and physiotherapy led to rapid recovery. This case highlights that DM should be considered even without rash. Anti-NXP2 positivity, associated with the sine-dermatitis phenotype, aided in confirming the diagnosis. Early recognition and treatment were crucial to the good outcome.

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Publication Details

Journal
International Journal of Community Medicine and Public Health
Published
2025-06-30
DOI
https://doi.org/10.18203/2394-6040.ijcmph20252139
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
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article

Dermatomyositis sine dermatitis-an unusual non classical dermatomyositis with amyopathic myopathy tale: a case report

G. Ramya Balaprabha, Prabhdeep Kaur, P. Neerajakshi, G. Nivas Kumar
International Journal of Community Medicine and Public Health
Inflammatory Myopathies and Dermatomyositis
article

Dermatomyositis sine dermatitis-an unusual non classical dermatomyositis with amyopathic myopathy tale: a case report

G. Ramya Balaprabha, Prabhdeep Kaur, P. Neerajakshi, G. Nivas Kumar
article en

Abstract

We report a 13-year-old girl with dermatomyositis sine dermatitis (DMSD), a rare form of juvenile DM characterized by muscle weakness without skin rash. She presented with 2 months of progressive proximal limb weakness, neck weakness, and bilateral hand paresthesias, but no skin findings. Laboratory tests showed elevated inflammation with normal creatine kinase and significant hypokalemia. Myositis autoantibody testing revealed strongly positive anti-NXP2 and anti-Ku antibodies. A diagnosis of DMSD was made. High-dose corticosteroids plus supportive care and physiotherapy led to rapid recovery. This case highlights that DM should be considered even without rash. Anti-NXP2 positivity, associated with the sine-dermatitis phenotype, aided in confirming the diagnosis. Early recognition and treatment were crucial to the good outcome.

International Journal of Community Medicine and Public HealthVol. 12(7)
P.V. Narsimha Rao Telangana Veterinary University (IN), CMR University (IN)
Openalex Percentile: Top 78%
Inflammatory Myopathies and Dermatomyositis
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Dermatomyositis sine dermatitis-an unusual non classical dermatomyositis with amyopathic myopathy tale: a case report — G. Ramya Balaprabha, Prabhdeep Kaur, et al. · International Journal of Community Medicine and Public Health (2025) | TGRS Research Map | TGRS