A Genetic Origin? Purpura Fulminans.

作者信息

Avnery Orly, Kenet Gili, Ellis Martin H

机构信息

Hematology Institute, Meir Medical Center, Kfar Saba, Israel; Sackler School of Medicine, Tel Aviv, Israel.

Sackler School of Medicine, Tel Aviv, Israel; National Hemophilia Center and Institute of Thrombosis and Hemostasis, Chaim Sheba Medical Center at Tel Hashomer, Ramat Gan, Israel.

出版信息

Am J Med. 2019 Mar;132(3):327-328. doi: 10.1016/j.amjmed.2018.10.003. Epub 2018 Oct 24.

DOI:10.1016/j.amjmed.2018.10.003

PMID:30367859

Abstract

摘要

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相似文献

A Genetic Origin? Purpura Fulminans.

Am J Med. 2019 Mar;132(3):327-328. doi: 10.1016/j.amjmed.2018.10.003. Epub 2018 Oct 24.

Varicella-associated purpura fulminans and multiple deep vein thromboses: a case report.

J Nippon Med Sch. 2009 Jun;76(3):165-8. doi: 10.1272/jnms.76.165.

Diagnosis and management of neonatal purpura fulminans.

Semin Fetal Neonatal Med. 2011 Dec;16(6):318-22. doi: 10.1016/j.siny.2011.07.009. Epub 2011 Aug 11.

Chickenpox is not always benign: postvaricella purpura fulminans requires prompt and aggressive treatment.

Pediatr Emerg Care. 2010 Dec;26(12):932-4. doi: 10.1097/PEC.0b013e3181fe91cd.

Purpura fulminans: How varicella zoster can result in acquired protein S deficiency.

Int J Lab Hematol. 2021 Apr;43(2):146-147. doi: 10.1111/ijlh.13441. Epub 2020 Dec 20.

Vasculitis with nonpalpable purpura resembling purpura fulminans.

Clin Exp Nephrol. 2020 Feb;24(2):190-191. doi: 10.1007/s10157-019-01824-4. Epub 2019 Nov 27.

Purpura fulminans in congenital protein C deficiency successfully treated with fresh frozen plasma and thrombomodulin.

J Dermatol. 2018 Jun;45(6):e165-e166. doi: 10.1111/1346-8138.14194. Epub 2017 Dec 19.

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Arch Dis Child. 2011 Nov;96(11):1066-71. doi: 10.1136/adc.2010.199919. Epub 2011 Jan 12.

Rivaroxaban Causes Missed Diagnosis of Protein S Deficiency but Not of Activated Protein C Resistance (Factor V Leiden).

Arch Pathol Lab Med. 2018 Jan;142(1):70-74. doi: 10.5858/arpa.2016-0616-OA. Epub 2017 Sep 18.

Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency.

Acta Paediatr. 2005 Aug;94(8):1155-8. doi: 10.1111/j.1651-2227.2005.tb02063.x.