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) |
|---|---|
| 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
- General Medicine
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