Vanga Amaresh, Rana Amna Z, Kowalewska Jolanta, Rust Harlan
Nephrology, Eastern Virginia Medical School, 855 W Brambelton Ave, Norfolk, VA 23510, USA.
Eastern Virginia Medical School, Norfolk, VA, USA.
Case Rep Nephrol. 2019 Jun 13;2019:4983139. doi: 10.1155/2019/4983139. eCollection 2019.
ANCA (anti-neutrophil cytoplasmic antibody) vasculitides are systemic autoimmune diseases in which anti-neutrophilic cytoplasmic antibodies activate primed neutrophils, thereby generating an inflammatory cascade resulting in the damage of small sized blood vessels in various organs of the body, including the heart. Pleuropericardial involvement is underrecognized as a complication of ANCA vasculitis and is highlighted in this case report of a 51-year-old male who presented with an initial symptomatic presentation of pleuropericardial effusion progressing to pericardial tamponade in the setting of a later renal biopsy proven pauci-immune crescentic glomerulonephritis with high ANA titres along with positive cANCA (cytoplasmic ANCA) and PR3 (proteinase 3) antibodies. He was found to have acute renal failure which progressively got better with cyclophosphamide.
抗中性粒细胞胞浆抗体(ANCA)血管炎是一种全身性自身免疫性疾病,其中抗中性粒细胞胞浆抗体激活致敏的中性粒细胞,从而引发炎症级联反应,导致包括心脏在内的身体各个器官的小血管受损。胸膜心包受累作为ANCA血管炎的一种并发症未得到充分认识,在本病例报告中得到突出体现。该病例为一名51岁男性,最初表现为胸膜心包积液的症状,随后进展为心包填塞,同时伴有肾活检证实的寡免疫性新月体性肾小球肾炎、高抗核抗体滴度以及胞浆型ANCA(cANCA)和蛋白酶3(PR3)抗体阳性。他被发现患有急性肾衰竭,使用环磷酰胺治疗后病情逐渐好转。