Renal thrombotic microangiopathy in a patient with septic disseminated intravascular coagulation

Yusuke Sakamaki1, Konosuke Konishi, Koichi Hayashi

  • 1Department of Internal Medicine, Shizuoka Red Cross Hospital, 8-2 Otemachi, Aoi-Ku, Shizuoka-City, Shizuoka 420-0853, Japan. yusuke0225@dance.ocn.ne.jp.

BMC Nephrology
|November 28, 2013
PubMed
Abstract

Insights

Thrombotic microangiopathy (TMA) can develop after sepsis-induced disseminated intravascular coagulation (DIC), especially with low ADAMTS-13 activity. Plasma exchange offers a beneficial treatment for this secondary TMA.

Area of Science:

  • Nephrology
  • Hematology
  • Critical Care Medicine

Background:

  • The pathogenesis of thrombotic microangiopathy (TMA) in sepsis remains incompletely understood.
  • TMA is associated with organ damage in severe sepsis.
  • Reduced ADAMTS-13 activity is a potential risk factor for TMA development.

Observation:

  • An 86-year-old woman with pyelonephritis developed sepsis-induced disseminated intravascular coagulation (DIC).
  • Despite controlling infection and DIC, she experienced worsening renal failure, thrombocytopenia, and hemolytic anemia, suggesting TMA.
  • Plasma exchange led to significant clinical and laboratory improvements.

Findings:

  • The patient presented with secondary TMA superimposed on sepsis-induced DIC.
  • ADAMTS-13 activity was reduced (44%) but no inhibitor was detected.
  • Renal biopsy findings were consistent with TMA sequelae.
  • Persistent low ADAMTS-13 activity was noted post-treatment.

Implications:

  • This case highlights that TMA can occur secondary to sepsis-induced DIC.
  • Plasma exchange is a potentially effective treatment for this condition.
  • Clinicians should consider secondary TMA in patients with sepsis-induced DIC and indicative signs.

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