Unnikrishnan Dileep, Shaikh Nasreen, Sharayah Ahmad, Patton Chandler
Department of Internal Medicine, Monmouth Medical Center, Long Branch, New Jersey, USA.
BMJ Case Rep. 2018 Mar 13;2018:bcr-2017-223860. doi: 10.1136/bcr-2017-223860.
A 47-year-old woman with a medical history of Raynaud's phenomenon presented with fever, cough and shortness of breath. She was found to have left lower lobe consolidation and pleural effusion and was treated as a case of pneumonia. During the hospital course, her respiratory status worsened, and she was intubated on the third hospital day. To investigate the high A-a gradient, a Computerized Tomographic Pulmonary Embolism (CTPE) study was done which identified a large left lower pulmonary artery embolism. She was also found to have a new murmur, and an echocardiogram demonstrated a large lesion on tricuspid valve. However, multiple sets of her blood cultures came back consistently negative. Alternative diagnoses for culture-negative endocarditis were considered, and a full set of rheumatological workup was done. Laboratory tests were suggestive of antiphospholipid syndrome, hence the diagnosis of tricuspid valve Libman-Sacks endocarditis was made.
一名有雷诺现象病史的47岁女性,出现发热、咳嗽和呼吸急促症状。她被发现左肺下叶实变并伴有胸腔积液,被当作肺炎病例进行治疗。在住院过程中,她的呼吸状况恶化,于住院第三天进行了气管插管。为了探究高肺泡 - 动脉血氧分压差,进行了计算机断层扫描肺动脉栓塞(CTPE)检查,结果发现左肺下叶肺动脉有一个大的栓塞。还发现她出现了新的心脏杂音,超声心动图显示三尖瓣有一个大的病变。然而,她多次血培养结果均持续为阴性。考虑了血培养阴性的心内膜炎的其他诊断,并进行了全套风湿学检查。实验室检查提示抗磷脂综合征,因此诊断为三尖瓣利布曼 - 萨克斯心内膜炎。