AI Article Synopsis

  • This report details the first successful microvascular free tissue transfer in a patient with Evans Syndrome, which combines platelet deficiency and autoimmune anemia.
  • Microvascular surgery in such patients has a higher risk of complications due to potential bleeding and clotting issues.
  • The case emphasizes the need for customized treatment plans and careful management of coagulation-related conditions in patients with Evans Syndrome.

Article Abstract

In this report, we describe the first successful case of microvascular free tissue transfer in a patient with Evans Syndrome (ES), a rare form of idiopathic thrombocytopenic purpura (ITP) and associated autoimmune hemolytic anemia (AIHA). Microvascular surgery in the setting of ES is likely to have higher complication rates because of the increased risk of postoperative bleeding and free flap thrombosis. The case presented here opens up to the feasibility of microvascular reconstruction of patients with coagulation disorders like ES. Every effort should be made to control for hemolytic, thrombocytopenic, and thrombophilic states associated with ES. In the absence of evidence-based treatment guidelines for ES, personalized treatment protocols with high-dose corticosteroids, immunoglobulin, and postoperative anticoagulation regimen are highly recommended.

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Source
http://dx.doi.org/10.1055/s-0033-1348898DOI Listing

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