Practice of symptomatic treatment in the era of evidence-based medicine: report of 2 cases of diagnosis of Sheehan's syndrome delayed till eighth decade
Author(s) -
A. M. Wani,
W. M. Hussain,
Mousa Al Mejally,
Adel A. Banjar,
K. S. Ali,
A. M. Khoujah,
S. H. Raja,
M. G Bafaraj,
W. A. Miamini,
Mubeena Akhtar
Publication year - 2010
Publication title -
bmj case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.231
H-Index - 26
ISSN - 1757-790X
DOI - 10.1136/bcr.09.2009.2276
Subject(s) - lethargy , medicine , malaise , sheehan's syndrome , hypopituitarism , pediatrics , presentation (obstetrics) , coma (optics) , hypophysitis , surgery , pituitary gland , physics , hormone , optics
Sheehan's syndrome, first described in 1937, is characterised by postpartum haemorrhage, pituitary necrosis, lactational failure and hypopitutarism. Presentation is variable and late presentations are not unusual due to partial ischaemic injury of the pituitary and gradual loss of endocrine function. A history of postpartum haemorrhage is usual but in some cases it is not elicited. Presentations such as malaise, fatigue, hypoglycaemia, decline in cognition, hyponatraemia, pancytopoenia, osteoporosis, secondary infertility, confusion and coma have all been reported. Two interesting cases of Sheehan's syndrome are presented that were diagnosed in the eighth decade; one due to atypical presentation of recurrent hyponatraemia and confusion, another from hypoglycaemic coma and symptoms of malaise and lethargy.
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