| Literature DB >> 24842349 |
Naresh Kumar1, Pratap Singh2, Jyoti Kumar3, Dinesh Kumar Dhanwal4.
Abstract
Sheehan syndrome is a rare but potentially serious complication of postpartum haemorrhage. The diagnosis can often be delayed by many years as symptoms may be subtle. We report the case of a 45-year-old woman who presented to the medical emergency unit with acute onset altered sensorium. On further evaluation she was found to have severe hypoglycaemia which was corrected by giving intravenous dextrose. On detailed clinical evaluation, she had a history of agalactia and amenorrhoea following her last pregnancy which was 15 years ago. She had a history of excessive postpartum bleeding during her last delivery. MRI of the brain showed empty sella and hormonal evaluation revealed adenohypophyseal insufficiency as evident from decreased levels of cortisol, thyroid-stimulating hormone, triiodothyronine, free thyroxine, follicle-stimulating hormone, luteinising hormone and prolactin. Based on clinical, radiological and laboratory parameters her final diagnosis was Sheehan syndrome with hypoglycaemia. 2014 BMJ Publishing Group Ltd.Entities:
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Year: 2014 PMID: 24842349 PMCID: PMC4039796 DOI: 10.1136/bcr-2013-200991
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X