Systemic sclerosis complicated with renal thrombotic microangiopathy: a case report and literature review

BMC Nephrol. 2022 Jan 10;23(1):22. doi: 10.1186/s12882-021-02639-w.

Abstract

Background: Systemic sclerosis (SSc) may overlap with other connective tissue diseases, which is named overlap syndrome. Scleroderma renal crisis (SRC) is a rare but severe complication of SSc. SSc related thrombotic microangiopathy (SSc-TMA) is an infrequent pathology type of SRC, while SSc-TMA accompanied by overlap syndrome is very rare.

Case presentation: This study reported a case of acute kidney injury (AKI) accompanied with overlap syndrome of SSc, systemic lupus erythematosus (SLE) and polymyositis (PM). The renal pathology supported the diagnosis of SSc-TMA but not SLE or PM-related renal injury, characterized by renal arteriolar thrombosis, endothelial cells edema, little cast in tubules and mild immune complex deposition. The primary TMA related factors (ADAMTS13 and complement H factor) were normal. Thus, this case was diagnosed as secondary TMA associated with SSc. The patient was treated with renin angiotensin system inhibitors, sildenafil, supportive plasma exchange/dialysis, and rituximab combined with glucocorticoids. After 2 months of peritoneal dialysis treatment, her renal function recovered and dialysis was stopped.

Conclusion: This study presented a case of SSc-TMA with overlap syndrome. Rituximab can be used as a treatment option in patients with high SRC risk or already manifesting SRC.

Keywords: Case report; Overlap syndrome; Scleroderma renal crisis; Systemic sclerosis; Thrombotic microangiopathy.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Female
  • Humans
  • Scleroderma, Systemic / etiology*
  • Thrombotic Microangiopathies / complications*
  • Young Adult