Acquired von Willebrand's disease and hypothyroidism: report of a case presenting with menorrhagia.

Abstract:

:A 17 year old woman presented with severe anaemia due to menorrhagia. On investigation, she was shown to have abnormalities of her haemostatic mechanism consistent with von Willebrand's disease Type I, although there was no family history of this disorder. In addition, she was shown to have severe primary hypothyroidism. On correction of hypothyroidism with oral thyroxine, her coagulation defects returned to normal and menorrhagia ceased. This is consistent with acquired von Willebrand's disease secondary to hypothyroidism.

journal_name

Postgrad Med J

authors

Blesing NE,Hambley H,McDonald GA

doi

10.1136/pgmj.66.776.474

subject

Has Abstract

pub_date

1990-06-01 00:00:00

pages

474-6

issue

776

eissn

0032-5473

issn

1469-0756

journal_volume

66

pub_type

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