Literature DB >> 31451452

Factor XIII deficiency with intracranial haemorrhage.

Muzamil Ejaz1, Ayesha Saleem1, Nimrah Ali1, Fizza Tariq1.   

Abstract

A 5-year-old girl presented to paediatric emergency with fever and seizures for a short duration. At first, meningitis was suspected and management was started empirically. There was no improvement in the clinical condition of the patient and investigations revealed spontaneous intracranial haemorrhage (ICH) secondary to factor XIII deficiency. The child was transfused cryoprecipitate and managed conservatively for ICH. She became asymptomatic and was kept on monthly cryoprecipitate transfusions. This case report summarises factor XIII deficiency in ICH which was not suspected initially, but diagnosed later on after CT scan head and factor XIII assay. This report also highlights events occurring during its management. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  haematology (incl blood transfusion); neurology; paediatrics

Mesh:

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Year:  2019        PMID: 31451452     DOI: 10.1136/bcr-2018-228682

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  1 in total

Review 1.  [Hereditary coagulation factor XIII deficiency: three cases report and literaure review].

Authors:  P P Xu; B J Ding; M J Li; J P Liu; L Liu; A Xia; W Q Liu; K S Zhou; H F Zhao; H Zhou; Y P Song
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2021-03-14
  1 in total

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