Literature DB >> 26965409

Bilateral adrenal haemorrhage: a cause of haemodynamic collapse in heparin-induced thrombocytopaenia.

Nasir Saleem1, Mahjabeen Khan1, Sanober Parveen1, Arvind Balavenkatraman1.   

Abstract

Heparin-induced thrombocytopaenia (HIT) is a life-threatening complication of exposure to heparin. It is mediated by autoantibodies to platelet factor-4 causing platelet activation, destruction and thrombosis. Given their rich arterial supply and a single central vein, the adrenal glands are particularly susceptible to congestive haemorrhage following venous thrombosis. We report a case of bilateral adrenal haemorrhage (BAH) associated with HIT following prophylactic use of unfractionated heparin for venous thromboembolism causing adrenal insufficiency. BAH is a life-threatening paradoxical complication associated with HIT, a prothrombotic state. The resulting adrenal insufficiency can lead to haemodynamic collapse if unrecognised. Early diagnosis, in the wake of vague symptoms, and prompt treatment primarily aimed at repletion of glucocorticoids and close monitoring of enlarging haemorrhage is of utmost importance. Likewise, early identification of HIT is important to prevent potential complications including adrenal haemorrhage. 2016 BMJ Publishing Group Ltd.

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Year:  2016        PMID: 26965409      PMCID: PMC4800239          DOI: 10.1136/bcr-2016-214679

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


  18 in total

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Journal:  Blood       Date:  2008-10-01       Impact factor: 22.113

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Journal:  J Clin Invest       Date:  1994-01       Impact factor: 14.808

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5.  Hyponatremia after anticoagulant treatment: a rare cause of adrenal failure

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