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Rare case of Antisynthetase syndrome presenting as interstitial lung disease-A report

Rare case of Antisynthetase syndrome presenting as interstitial lung disease-A report

A rare case of Antisynthetase syndrome presenting as interstitial lung disease was reported in the Journal of Medical Case Reports.

Antisynthetase syndrome is a relatively uncommon entity and can be easily missed if not specifically looked for in adults whose initial presentation is with interstitial lung disease. Its presentation with interstitial lung disease alters its prognosis.

This case report describes a 27-year-old Pakistani, Asian man, a medical student, with no previous comorbidities or significant family history who presented with a 3 months’ history of low-grade fever and lower respiratory tract infections, associated with exertional dyspnea, arthralgias, and gradual weight loss.

During these 3 months, he had received multiple orally administered antibiotics for suspected community-acquired pneumonia. When he presented to us, he was pale and febrile. A chest examination was significant for bi-basal end-inspiratory crackles. Preliminary investigations revealed raised erythrocyte sedimentation rate.

High resolution computed tomography (CT) of his chest showed fine ground-glass attenuation in posterior basal segments of both lower lobes suggestive of interstitial lung disease. He was started on dexamethasone, to which he responded and showed improvement. However, during the course of events, he developed progressive proximal muscle weakness.


CT scan showing areas of ground-glass haze and traction bronchiectasis

Further investigations revealed raised creatinine phosphokinase and lactate dehydrogenase. A thorough autoimmune profile was carried out which showed positive anti-Jo-1 antibodies in high titers. A muscle biopsy was consistent with inflammatory myopathy. Clinical, radiological, serological, and histopathological markers aided in making the definitive diagnosis of the antisynthetase syndrome. Antisynthetase syndrome is a variant of polymyositis but with visceral involvement, that is, interstitial lung disease and positive anti-Jo-1 antibodies. Our patient responded very well to glucocorticoids and azathioprine.

“Antisynthetase syndrome is a rare clinical entity which apart from clinical presentation requires specific serological investigations for diagnosis. Concomitant association of interstitial lung disease gives it a guarded prognosis.” concluded the authors

For reference, please click on the link

Journal of Medical Case Reports

Source: self

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