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Severe hypertension with renal thrombotic microangiopathy: what happened to the usual suspect?
Author(s) -
Steven Van Laecke,
Wim Van Biesen
Publication year - 2017
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1016/j.kint.2017.02.025
Subject(s) - thrombotic microangiopathy , atypical hemolytic uremic syndrome , eculizumab , medicine , concomitant , complement system , immunology , antibody , disease
Patients with atypical hemolytic uremic syndrome (aHUS) and malignant hypertension can both present with concomitant hypertension and thrombotic microangiopathy (TMA), rendering policy decisions complex. Timmermans et al. report that patients with severe hypertension and renal TMA might have unrecognized aHUS with underlying complement abnormalities. Based on this, they assert that all patients presenting with severe hypertension and renal TMA should be evaluated for aHUS. It remains uncertain whether this holds equally true for patients with malignant hypertension and renal TMA.

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