Scleroderma renal crisis with overlap to dermatomyositis triggered by COVID-19 infection: a case report.

Scleroderma renal crisis with overlap to dermatomyositis triggered by COVID-19 infection: a case report.

Publication date: Sep 06, 2025

A 46-year-old man was diagnosed with anti jo-1 antibody-positive dermatomyositis 11 years ago and had been treated with prednisolone and tacrolimus. In the present case, after contracting SARS CoV2 virus infection, his dyspnea rapidly worsened, and he presented with renal and cardiac failure. Based on the biopsy results of the same area and anti-U1-RNP antibody positivity, he was diagnosed with systemic sclerosis and scleroderma renal crisis and required hemodialysis. A renal biopsy performed later showed tubular atrophy, intratubular cell debris, and endothelial cell damage, consistent with scleroderma renal crisis. Although rapid skin hardening and high-dose glucocorticoid use are known risks for scleroderma renal crisis, scleroderma renal crisis triggered by novel SARS CoV-2 virus infection has never been reported before and is very rare. It is crucial to identify the relationship between the scleroderma renal crisis and SARS CoV-2 virus infection. This relationship can be explained through the RAS system, which is believed to play a role in the development of both.

Concepts Keywords
11years Renin angiotensin system
Cardiac SARS-CoV-2virus
Dermatomyositis Scleroderma renal crisis
Renal Systemic sclerosis
Virus

Semantics

Type Source Name
disease MESH dermatomyositis
disease MESH COVID-19
disease MESH infection
drug DRUGBANK Prednisolone
drug DRUGBANK Tacrolimus
disease MESH virus infection
disease MESH dyspnea
disease MESH cardiac failure
disease MESH systemic sclerosis
disease MESH atrophy
disease IDO cell
drug DRUGBANK Rasagiline
disease IDO role

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