A Sudden Onset of Severe Thrombocytopenia While Using Evolocumab

Author:

Inoue Ikuo1ORCID,Takenaka Yasuhiro12ORCID,Kin Yoshitora3,Yamazaki Satoshi4,Ikegami Yuichi1,Saito Daigo1,Shimada Akira1ORCID

Affiliation:

1. Department of Endocrinology and Diabetes, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama, Iruma, Saitama 350-0495, Japan

2. Department of Physiology, Graduate School of Medicine, Nippon Medical School, 1-25-16 Nezu, Bunkyo, Tokyo 113-0031, Japan

3. Department of Internal Medicine, Fukaya Red Cross Hospital, 5-8-1 Kamishibatyohnishi, Fukaya, Saitama 366-0052, Japan

4. Kumagaya-geka Hospital, 3811-1 Sayata, Kumagaya, Saitama 360-0023, Japan

Abstract

A 72-year-old man with a 10-year history of coronary heart disease started evolocumab treatment once a month after developing excess myalgia due to therapy with a 3-hydroxy-methylglutaryl CoA reductase inhibitor. No side effects such as myalgia symptoms had been reported during the first 14 months of evolocumab treatment; however, he suddenly presented with acute severe thrombocytopenia following the 14th treatment. His platelet count continued to decrease to a nadir of 1,000/μL. His platelet-associated immunoglobulin G level had elevated to 790 ng/107 cells. He started receiving a combination of steroid therapy, high-dose immunoglobulin therapy, and platelet transfusions, but the first-line therapy was ineffective. He was subsequently treated with a thrombopoietin receptor agonist, and his platelet count recovered to 250,000/μL.

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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