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Autopsy case of sudden maternal death from thrombotic thrombocytopenic purpura.

作者信息

Yamamoto Takuma, Fujimura Yoshihiro, Emoto Yuko, Kuriu Yukiko, Iino Morio, Matoba Ryoji

机构信息

Department of Legal Medicine, Osaka University Graduate School of Medicine, Osaka Department of Blood Transfusion Medicine, Nara Medical University, Nara, Japan.

出版信息

J Obstet Gynaecol Res. 2013 Jan;39(1):351-4. doi: 10.1111/j.1447-0756.2012.01941.x. Epub 2012 Jul 6.

DOI:10.1111/j.1447-0756.2012.01941.x
PMID:22765161
Abstract

A 31-year-old pregnant woman was transferred to the emergency room at 27 weeks of gestation. She had one-day history of fever and upper abdominal pain. Soon after admission, she underwent cardiopulmonary arrest. Autopsy was performed and multiple microthrombi were seen within the small-caliber vessels of many organs, but not in the lungs. Immunohistochemical staining revealed that the thrombi were rich in von Willebrand factor. We also obtained results which showed severely deficient plasma a disintegrin-like and metalloprotease with thrombospondin motifs (ADAMTS) 13 activity and positive ADAMTS13 inhibitor, confirming a diagnosis of thrombotic thrombocytopenic purpura. As far as we know, in Japan, this is the first autopsy report of sudden maternal death from thrombotic thrombocytopenic purpura. We expect that the routine laboratory application of ADAMTS13 assays for unknown thrombocytopenic patients during pregnancy may help in differential diagnosis at an earlier stage of the disease and facilitate tailor-made therapeutic intervention.

摘要

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