Acquired Combined Factor Deficiency: Case Report

Clinical Laboratory
|September 9, 2020
PubMed
Abstract

Insights

A patient with acquired hemophilia due to superwarfarin (anticoagulant rodenticide) poisoning experienced multiple factor deficiencies. Immunosuppressive treatment and plasmapheresis were effective when factor replacement failed.

Area of Science:

  • Hematology
  • Toxicology
  • Internal Medicine

Background:

  • Acquired hemophilia is a rare bleeding disorder.
  • Difenacoum, a superwarfarin anticoagulant, is a common rodenticide.
  • Inhibition of vitamin K-dependent factors (II, VII, IX, X) is a known effect.

Observation:

  • A patient presented with hematuria and prolonged coagulation tests.
  • The patient had deficiencies in multiple coagulation factors (II, V, VII, VIII, IX, X, XI, XII).
  • Autoantibodies including antinuclear, antiphospholipid, and anti-dsDNA antibodies were detected.

Findings:

  • Exposure to difenacoum (superwarfarin) rat poison was confirmed.
  • Initial replacement therapy with fresh frozen plasma, vitamin K, and prothrombin complex concentrate was insufficient.
  • Inhibitors against factor VIII and factor IX were present, necessitating plasmapheresis and immunosuppressive treatment.

Implications:

  • Plasmapheresis and immunosuppressive therapy can be effective for acquired factor deficiency when factor replacement is insufficient.
  • This case highlights the potential for superwarfarin poisoning to cause complex coagulopathy.
  • Early diagnosis and targeted treatment are crucial for managing rare bleeding disorders.

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