Abstract
A patient with hereditary hemorrhagic telangiectasia manifested recurrent gastrointestinal bleeding aggravated by an acquired factor VIII inhibitor. Immunosuppressive therapy with cyclophosphamide and prednisone successfully corrected the coagulation defect.
Original language | English (US) |
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Pages (from-to) | 623-624 |
Number of pages | 2 |
Journal | Southern Medical Journal |
Volume | 78 |
Issue number | 5 |
DOIs | |
State | Published - Jan 1 1985 |
ASJC Scopus subject areas
- Medicine(all)