THA in Patients with Idiopathic Thrombocytopenic Purpura (ITP): A Case Report

  • Suzuki K
  • Kawachi S
  • Nanke H
  • et al.
N/ACitations
Citations of this article
9Readers
Mendeley users who have this article in their library.

Abstract

We report a case of idiopathic thrombocytopenic purpura (ITP) accompanied by steroid-induced avascular necrosis of the femoral head in a 68-year-old woman. Extremely low platelet counts of ITP patients prohibit any surgical interventions. Her platelet count was 25,000/μL. We performed a total hip arthroplasty with high-dose immunoglobulin therapy and transfusion of platelet concentrates. Her platelet count increased to 94,000/μL just before the operation. No hemostatic complications were encountered perioperatively, and the postoperative course was uneventful. She left the hospital 20 days after the operation with a T-cane. Her platelet count decreased to 34,000/μL on the day she left the hospital. Three years after the operation, she had no groin pain and could walk without ambulatory assistive devices. We did not observe implant loosening.

Cite

CITATION STYLE

APA

Suzuki, K., Kawachi, S., Nanke, H., & Ito, T. (2011). THA in Patients with Idiopathic Thrombocytopenic Purpura (ITP): A Case Report. Journal of Rural Medicine, 6(2), 81–83. https://doi.org/10.2185/jrm.6.81

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free