진성다혈구증과 병발된 IgA 신증 1예

Polycythemia Vera is a hematopoietic stem cell dis- ease, characterized by sustained and excessive prolif- eration of erythrocytic, granurocytie and megakar- yocytic cells in the bone marrow resulting in pancy- tosis in peripheral blood. Patient with Polycytopenia Vera usually present with symptoms...

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Veröffentlicht in:Kidney research and clinical practice 1994-01, Vol.13 (4), p.977
Hauptverfasser: 김영묵, 이충원, 오정열, 최정숙, 류수현, 임종섭, 유대성, 제영성, 주종은
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Sprache:kor
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Zusammenfassung:Polycythemia Vera is a hematopoietic stem cell dis- ease, characterized by sustained and excessive prolif- eration of erythrocytic, granurocytie and megakar- yocytic cells in the bone marrow resulting in pancy- tosis in peripheral blood. Patient with Polycytopenia Vera usually present with symptoms referable to an expanded blood volume. We experieneed a patient who presented with headache, dizziness, and syncopal attack coexistion with renal symptoms, as hematuria, proteinuria, and generalized edema. We confirmed this patient to Polycythemia Vera by Polycythemia Vera Study Group criteria and IgA Nephropathy by renal biopsy. No other reports have been seen in the literature on Polycythemia Vera associated with IgA Nephropathy. Recently, We experienced a Polycythe- mia Vera associated with IgA Nephropsthy and re- port this case with brief review of literature.
ISSN:2211-9132