| Literature DB >> 31289158 |
Supriya Sharma1, Rakesh Kumar Chak1, Richa Khanna1.
Abstract
The Bernard-Soulier syndrome also known as hemorrhagioparous thrombocytic dystrophy, is a rare autosomal recessive bleeding disorder. Macrothrombocytopenia and increased bleeding time are the two main features of this syndrome. There is a reduced adherence of giant platelets to the subendothelium due to a deficiency of glycoprotein GPIb-V-IX complex. Routine dental extraction in a patient with a bleeding disorder can lead to life-threatening complications and there are very few specific protocols for the same. Here, we present a case report describing haemostasis management during dental extraction in a 7-year-old female child, suffering from this syndrome. It was observed that the preoperative and postoperative human leucocyte antigen-matched platelet transfusion, systemic intraoperative tranexamic acid and minimally traumatic procedure improved bleeding control and management. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: congenital disorders; dentistry and oral medicine; haematology (incl blood transfusion)
Mesh:
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Year: 2019 PMID: 31289158 PMCID: PMC6615838 DOI: 10.1136/bcr-2018-229082
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X