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A rare case of alveolar hemorrhage with hypertensive emergency

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Introduction: Alveolar hemorrhage presents with severe respiratory failure, requiring prompt diagnosis and treatment. Alveolar hemorrhage is often caused by autoimmune diseases accompanied by progressive renal dysfunction. However, few cases without autoimmune diseases occur, making diagnosis difficult. Here, we report a case of alveolar hemorrhage with hypertensive emergency. Patient concerns: A 28-year-old man presented with dyspnea and bloody sputum. His blood pressure was 200/120 mm Hg. Diagnosis: The chest computed tomography showed suggestive of alveolar hemorrhage. Renal dysfunction and proteinuria were observed. However, autoantibodies were not detected. Echocardiogram revealed left ventricular function decrease. Ejection fraction was 20% to 30% with no ventricular asynergy or any valvular diseases. Brain magnetic resonance imaging showed hyperintense lesions on fluid-attenuated inversion recovery in the white matter of both cerebral and right cerebellar hemispheres, which were compatible with posterior reversible encephalopathy syndrome. Renal biopsy did not reveal any immune-mediated glomerulonephritis or vasculitis, but hypertensive nephropathy was diagnosed. Interventions: Blood pressure was controlled with combination therapy using calcium channel blocker, angiotensin II receptor blocker, α1 blocker, and β blocker. Outcomes: Alveolar hemorrhage and proteinuria improved with strict blood pressure control. Conclusion: This case indicates that severe hypertension can possibly cause alveolar hemorrhage. Accumulating these cases is important for general physicians to diagnose the alveolar hemorrhage with hypertensive emergency in its early stage and to avoid unnecessary treatment such as immunosuppressive therapy.
Title: A rare case of alveolar hemorrhage with hypertensive emergency
Description:
Introduction: Alveolar hemorrhage presents with severe respiratory failure, requiring prompt diagnosis and treatment.
Alveolar hemorrhage is often caused by autoimmune diseases accompanied by progressive renal dysfunction.
However, few cases without autoimmune diseases occur, making diagnosis difficult.
Here, we report a case of alveolar hemorrhage with hypertensive emergency.
Patient concerns: A 28-year-old man presented with dyspnea and bloody sputum.
His blood pressure was 200/120 mm Hg.
Diagnosis: The chest computed tomography showed suggestive of alveolar hemorrhage.
Renal dysfunction and proteinuria were observed.
However, autoantibodies were not detected.
Echocardiogram revealed left ventricular function decrease.
Ejection fraction was 20% to 30% with no ventricular asynergy or any valvular diseases.
Brain magnetic resonance imaging showed hyperintense lesions on fluid-attenuated inversion recovery in the white matter of both cerebral and right cerebellar hemispheres, which were compatible with posterior reversible encephalopathy syndrome.
Renal biopsy did not reveal any immune-mediated glomerulonephritis or vasculitis, but hypertensive nephropathy was diagnosed.
Interventions: Blood pressure was controlled with combination therapy using calcium channel blocker, angiotensin II receptor blocker, α1 blocker, and β blocker.
Outcomes: Alveolar hemorrhage and proteinuria improved with strict blood pressure control.
Conclusion: This case indicates that severe hypertension can possibly cause alveolar hemorrhage.
Accumulating these cases is important for general physicians to diagnose the alveolar hemorrhage with hypertensive emergency in its early stage and to avoid unnecessary treatment such as immunosuppressive therapy.

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