Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 1990 Jul;66(777):560-2.
doi: 10.1136/pgmj.66.777.560.

Acquired von Willebrand disease associated with free lambda light chain monoclonal gammopathy, normal bleeding time and response to prednisone

Affiliations
Case Reports

Acquired von Willebrand disease associated with free lambda light chain monoclonal gammopathy, normal bleeding time and response to prednisone

A K Stewart et al. Postgrad Med J. 1990 Jul.

Abstract

We report a case of acquired von Willebrand's syndrome with severe gastrointestinal bleeding and associated free monoclonal lambda light chains. The patient had a rapid sustained clinical and laboratory response to the administration of prednisone. Of note in this patient was the occurrence of angiodysplasia which has previously been reported in association with acquired von Willebrand's syndrome. No inhibitors of VWF:Ag, VWF:RCoF, or factor VIII:C were detected by mixing studies and the bleeding time was normal. Very few high molecular weight von Willebrand multimers were present prior to prednisone; however, the pattern reverted to a normal distribution following treatment. In appropriate patients with acquired von Willebrand's syndrome and monoclonal para-proteins, a trial of prednisone may be indicated.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Am J Med. 1979 Oct;67(4):693-6 - PubMed
    1. J Clin Pathol. 1979 Oct;32(10):1030-5 - PubMed
    1. Br J Haematol. 1980 May;45(1):161-4 - PubMed
    1. Br J Haematol. 1980 Nov;46(3):503-6 - PubMed
    1. Blood. 1981 Oct;58(4):665-9 - PubMed

Publication types