Maloney Kaylah D, Balakumar Arjun, McGann Sean, Zhang Xiao Chi
Emergency Medicine, Thomas Jefferson University Hospital, Philadelphia, USA.
Emergency Medicine, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, USA.
Cureus. 2019 Nov 26;11(11):e6239. doi: 10.7759/cureus.6239.
Calcium pyrophosphate dihydrate (CPPD) crystal deposition disease or pseudogout is an idiopathic articular disease that predominantly affects elderly patients. It is caused by a systemic deposition of calcium pyrophosphate (CPP) crystals in the articular and hyaline joint cartilage. The majority of cases present as chronic arthritis, but a subset of CPPD can present as rapid onset of sharp pain and joint swelling, posing a diagnostic challenge. We present a case of a 64-year-old man with a history of hypertension, urologic cancer, and gout presenting to the emergency department (ED) with a sudden-onset, severe stabbing right shoulder pain radiating to the neck and upper back. On ED arrival, he was mildly hypotensive, afebrile, diaphoretic, and uncomfortable, causing concern for aortic dissection. His exam was significant for limited shoulder range of motion; his sensation, strength, and distal pulses were intact and equal in bilateral upper extremities. His plain films showed multilevel cervical degenerative disc disease and facet arthrosis and right glenohumeral osteoarthritis without fracture or malalignment. A computed tomography (CT) angiogram was negative for vascular anomalies. Throughout his ED stay, his pain was refractory to medication, and he developed a new fever, prompting a targeted shoulder ultrasound; this revealed large glenohumeral effusion, and synovial analysis revealed CPP crystals without organism growth. This case illustrates an unusual acute CPPD attack that mimicked an aortic dissection. Emergency physicians should recognize both common and uncommon presentations for chronic disease processes in maintaining a broad differential diagnosis and delivering quick, targeted treatment.
二水焦磷酸钙(CPPD)晶体沉积病或假性痛风是一种特发性关节疾病,主要影响老年患者。它是由焦磷酸钙(CPP)晶体在关节和透明关节软骨中的系统性沉积引起的。大多数病例表现为慢性关节炎,但一小部分CPPD病例可表现为突发剧痛和关节肿胀,这对诊断构成挑战。我们报告一例64岁男性患者,有高血压、泌尿系统癌症和痛风病史,因突发严重的右肩部刺痛并放射至颈部和上背部而就诊于急诊科。到达急诊科时,他轻度低血压,无发热,多汗,且感觉不适,这引起了对主动脉夹层的担忧。他的检查结果显示肩部活动范围受限;双侧上肢的感觉、力量和远端脉搏均正常且相等。他的X线平片显示多节段颈椎间盘退变疾病、小关节病和右肩肱关节骨关节炎,无骨折或畸形。计算机断层扫描(CT)血管造影未发现血管异常。在他留观急诊科期间,他的疼痛对药物治疗无效,并且出现了新的发热,这促使进行了针对性的肩部超声检查;结果显示肩肱关节有大量积液,滑膜分析发现了CPP晶体,未发现微生物生长。该病例说明了一次不寻常的急性CPPD发作,其表现类似主动脉夹层。急诊医生在保持广泛的鉴别诊断并提供快速、有针对性的治疗时,应认识到慢性病过程的常见和不常见表现。