{Reference Type}: Case Reports
{Title}: Autosomal dominant polycystic kidney disease and pericardial effusion: coincidence? I think not! Case report and review of the literature.
{Author}: Rigamonti E;Caruzzo CA;Valotta A;Caretta A;Scopigni FR;
{Journal}: Eur Heart J Case Rep
{Volume}: 8
{Issue}: 4
{Year}: 2024 Apr
暂无{DOI}: 10.1093/ehjcr/ytae144
{Abstract}: <B>UNASSIGNED: </B>Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary disease causing chronic renal failure, with a high incidence of extra-renal manifestations including pericardial effusion.<BR><B>UNASSIGNED: </B>We present the case of a 41-year-old female, known for ADPKD, who presented to our emergency department with epigastric pain radiating to the interscapular area. Blood exams showed moderate increase in inflammatory markers. Echocardiography revealed a circumferential pericardial effusion of 10 mm. She was put under treatment with colchicine therapy (1 mg b.i.d.) based on a presumptive diagnosis of acute pericarditis with pericardial effusion. She was hospitalized due to increase in pericardial effusion, underwent pericardial drainage, and started prednisone therapy with rapid recovery. We started a close follow-up on a monthly basis, with progressive decrease in pericardial effusion and progressive amelioration in symptoms, although the patient continued to report mild asthenia.<BR><B>UNASSIGNED: </B>Pericardial effusion and ADPKD are conditions that both require an interdisciplinary discussion for optimal patient care that avoids neglecting pivotal symptoms and avoidable invasive examinations.