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hypertensive retinopathy/muntah
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Hypertensive Retinopathy Secondary to Anlotinib Treatment
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Purpose: We report a case of a middle-aged woman who developed hypertensive retinopathy following oral administration of Anlotinib.
Observations: A 48-year-old woman presented
Is reversible posterior leukoencephalopathy with severe hypertension completely reversible in all patients?
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Leukoencephalopathy with severe hypertension is a recently described entity in nephrology, with only a few case reports to date in children. We prospectively studied 18 children with severe hypertension to evaluate the clinical features, severity, reversibility, and prognosis. All were subjected to
Iatrogenically induced hypertensive encephalopathy.
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A 49-year-old female with a 30-year history of untreated essential hypertension was noted to have a blood pressure of 290/175 mmHg during evaluation for elective gynecological surgery. At the time of hospitalization she complained chiefly of chronic frontal headaches. Physical examination revealed
Thrombotic microangiopathy as a complication in a patient with focal segmental glomerulosclerosis.
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We report on a 12-year-old female patient with steroid-dependent nephrotic syndrome due to focal segmental glomerulosclerosis (FSGS) since her 3rd year of life. She was twice treated with oral cyclophosphamide and received antihypertensive treatment with atenolol and enalapril. After 3 years without
Spectrum of radiological changes in hypertensive children with reversible posterior leucoencephalopathy.
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We prospectively studied 19 children with severe hypertension to evaluate the spectrum of radiological changes, severity and reversibility of this entity. All of them were subjected to clinical and biochemical evaluation, followed by magnetic resonance imaging (MRI) and magnetic resonance
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