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Malignant Hypertension and Thrombotic Thrombocytopenic Purpura: False Friends

Challenging differential diagnosis, Rare disease

Hossam Abdalla, Mostafa Alfishawy, Michael Babigumira, Tayyaba Bashir

(Department of Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, Queens, NY, USA)

Am J Case Rep 2015; 16:374-376

DOI: 10.12659/AJCR.892787

Published: 2015-06-17


BACKGROUND: Thrombotic thrombocytopenic purpura (TTP) is a rare hematologic disorder resulting in hemolysis of red blood cells, consumption of platelets, and occlusion of microvasculature. Malignant hypertension is the clinical syndrome of severe elevations in blood pressure and funduscopic hypertensive retinopathy, including bilateral flame-shaped hemorrhage and papilledema.
CASE REPORT: We describe the case of a 63-year-old man who presented with features of TTP and malignant hypertension treated with plasma exchange and developing end-stage renal disease.
CONCLUSIONS: Given the diagnostic uncertainty at presentation, clinicians should quickly intervene to control hypertension and institute plasma exchange as needed.

Keywords: Blood Pressure - physiology, Biopsy, Diagnosis, Differential, Humans, Hypertension, Malignant - physiopathology, Male, Middle Aged, Purpura, Thrombotic Thrombocytopenic - physiopathology



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