Literature DB >> 26057201

Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.

Jie Yan1, Donghong Deng2, Meiling Luo1, Peng Cheng2, Bo Chi3, Yuan Yuan3, Lin Liao1, Faquan Lin4.   

Abstract

BACKGROUND: Dysfibrinogenemia is characterized by dysfunction induced by an abnormal fibrinogen molecule structure that results in blood coagulation dysfunction. The clinical manifestations are diverse. Dysfibrinogenemia is misdiagnosed or miss diagnosis in the absence of an appropriate laboratory examination. Treatment during pregnancy or surgery is suggested to be adapted to the individual patient.
METHODS: A 26-y-old woman took drugs that may cause fetal malformation during early pregnancy. She required an artificial abortion in a local municipal hospital and was misdiagnosed with hypofibrinogenemia.
RESULTS: A preoperative coagulation test revealed a fibrinogen concentration of 0.56g/l, prompting a diagnosis of hypofibrinogenemia at the local municipal hospital. She underwent fresh plasma and cryoprecipitate infusion with a poor outcome. However, the coagulation test results in our hospital showed a prothrombin time of 12.60s, activated partial thromboplastin time of 34.60s, thrombin time of 25.30s, and fibrinogen concentrations of 0.51g/l (Clauss method) and 3.82g/l (immunoturbidimetry). Ultrasound examination showed early intrauterine pregnancy with a fetal heartbeat. The patient was finally diagnosed with dysfibrinogenemia. A detailed inquiry regarding her personal and family histories revealed no abnormal bleeding or thrombotic events. Therefore, other therapies were not conducted and operation was successfully performed. No abnormal bleeding or thrombotic events occurred postoperatively.
CONCLUSIONS: Simultaneous determination of fibrinogen concentrations using the Clauss method, prothrombin time-derived method, and immunoturbidimetry as well as measurement of the thrombin time, reptilase time, prothrombin time, activated partial thromboplastin time and so on can effectively distinguish dysfibrinogenemia from other diseases. Special treatment of asymptomatic dysfibrinogenemia is not needed during pregnancy or surgery in the absence of bleeding or thrombotic events in the patient's personal or family history.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Abortion; Dysfibrinogenemia; Literature review; Misdiagnosis

Mesh:

Year:  2015        PMID: 26057201     DOI: 10.1016/j.cca.2015.06.002

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  6 in total

1.  Combined use of Clauss and prothrombin time-derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia.

Authors:  Liqun Xiang; Meiling Luo; Jie Yan; Lin Liao; Weijie Zhou; Xuelian Deng; Donghong Deng; Peng Cheng; Faquan Lin
Journal:  J Clin Lab Anal       Date:  2017-09-18       Impact factor: 2.352

2.  A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release.

Authors:  Jie Yan; Meiling Luo; Peng Cheng; Lin Liao; Xuelian Deng; Donghong Deng; Faquan Lin
Journal:  Int J Hematol       Date:  2016-12-08       Impact factor: 2.490

Review 3.  Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions.

Authors:  Meiling Luo; Aiqiu Wei; Liqun Xiang; Jie Yan; Lin Liao; Xuelian Deng; Donghong Deng; Peng Cheng; Faquan Lin
Journal:  J Thromb Thrombolysis       Date:  2018-10       Impact factor: 2.300

4.  Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis.

Authors:  Shiyue Ma; Lingjian Tang; Chaoli Wu; Hui Tang; Xue Pu; Jinhong Niu
Journal:  Appl Bionics Biomech       Date:  2022-01-28       Impact factor: 1.781

5.  Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.

Authors:  Meiling Luo; Donghong Deng; Liqun Xiang; Peng Cheng; Lin Liao; Xuelian Deng; Jie Yan; Faquan Lin
Journal:  Medicine (Baltimore)       Date:  2016-09       Impact factor: 1.889

6.  Novel compound heterozygous SPTA1 mutations in a patient with hereditary elliptocytosis.

Authors:  Shiyue Ma; Jinqiu Qin; Aiqiu Wei; Xiaohong Li; Yuanyuan Qin; Lin Liao; Faquan Lin
Journal:  Mol Med Rep       Date:  2018-02-26       Impact factor: 2.952

  6 in total

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