Protein c deficiency (acquired) D68.5

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.10.2020

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Synonym(s)

Acquired protein C deficiency; Protein C deficiency

Definition
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Acquired deficiency or lack of protein C.

Classification
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In addition to congenital protein C deficiencies, there are also a number of exogenously caused protein C deficiencies:

  • Coumarin therapy
  • Asparaginase therapy in the context of leukemia treatment
  • in liver diseases, e.g. Budd-Chiari syndrome or venooclusive syndrome (VOD)
  • for consumption coagulopathy
  • after operations following polytrauma
  • for progressive renal insufficiency
  • for vitamin K deficiency
  • in sepsis
  • post-infectious (cloinical) symptoms 10-14 days after the first infection infections (e.g. varicella)
  • with massive blood loss
  • for chronic inflammatory bowel disease.

The protein C concentration can be increased in:

Etiopathogenesis
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Together with a coenzyme, protein S, the protein C/protein S system is activated via the thrombin-thrombomodulin complex in a negative feedback reaction and inhibits the activated factors V and VIII (Va, VIIIa) by proteolytic cleavage. Thus, the protein C/protein S system plays a key role in the inhibition of hemostasis, because with this action it controls the activation of factor X to Xa and thus of prothrombin to thrombin.

Literature
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  1. HA Neumann (2014) The coagulation system. ABW-Wissenschaftsverlag GmbH Berlin S. 219f.

Disclaimer

Please ask your physician for a reliable diagnosis. This website is only meant as a reference.

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Last updated on: 29.10.2020