Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal stem-cell disorder in which blood cells lack complement inhibiting membrane proteins, and become susceptible to complement-mediated injury, leading to chronic intravascular hemolysis and pancytopenia. Glucocorticoids have been a mainstay of
โฆ LIBER โฆ
Paroxysmal nocturnal hemoglobinuria terminating as erythroleukemia
โ Scribed by David E. Cowall; Dominick N. Pasquale; Paul Dekker
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 591 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
A case of a patient who developed erythroleukemia 3 years into the course of paroxysmal nocturnal hemoglobinuria (PNH) is presented. A case of erythroleukemia with a positive sucrose lysis test has been reported, but our case appears to be the first with a long clinical course of PNH evolving into erythroleukemia. The association between these two diseases, their possible clonal origin, and how they fit into the myelodysplastic syndromes are discussed.
Cancer 43:1914-1916, 1979.
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