B-cell Chronic Lymphocytic Leukemia is Complicated by Autoimmune Hemolytic Anemia and Anti-phospholipid Syndrome
We describe a rare case of a 68-year-old man with B-cell chronic lymphocytic leukemia (B-CLL) who developed autoimmune hemolytic anemia (AIHA) and anti-phospholipid syndrome (APS). On admission, he was diagnosed as having B-CLL and AIHA on the basis of CD5-positive B-lymphocytes infiltrated into his...
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Veröffentlicht in: | Journal of Clinical and Experimental Hematopathology 2002, Vol.42(2), pp.75-79 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We describe a rare case of a 68-year-old man with B-cell chronic lymphocytic leukemia (B-CLL) who developed autoimmune hemolytic anemia (AIHA) and anti-phospholipid syndrome (APS). On admission, he was diagnosed as having B-CLL and AIHA on the basis of CD5-positive B-lymphocytes infiltrated into his bone marrow and a positive Coombs test, respectively. Although the symptoms of B-CLL and AIHA were improved by chemotherapy, he developed deep-vein thrombosis, which was probably caused by a lupus anticoagulant. It was interesting that the thrombosis due to APS occurred following a decrease of hemolysis from AIHA after intensive chemotherapy. |
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ISSN: | 1346-4280 1880-9952 |
DOI: | 10.3960/jslrt.42.75 |