Ayyar Archana, Seaman Rachel D, Guntupalli Kalpalatha, Tolcher Mary C
Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USA.
Department of Medicine, Pulmonary and Critical Care, Baylor College of Medicine, Houston, Texas, USA.
Case Rep Obstet Gynecol. 2022 Mar 2;2022:4865985. doi: 10.1155/2022/4865985. eCollection 2022.
COPA syndrome is a rare autoimmune disease, demonstrating an autosomal dominant inheritance pattern with variable penetration that occurs more frequently in females than males. This disease manifests in childhood as pulmonary hemorrhage, arthritis, and renal disease.
We present a case of obstetric management of a 20-year-old nulligravida patient with a diagnosis of COPA syndrome. Her case was further complicated by multiple antepartum admissions for hypoxemia and a complex psychosocial history of substance use. On her first antepartum admission, rheumatology recommended management with hydroxychloroquine, inhaled corticosteroids (budesonide), and bronchodilators (albuterol inhaler) as needed. On admission for induction of labor, she was again noted to have oxygen desaturations. A chronic thrombus was noted on computed tomography (CT), and a multidisciplinary team was recommended against Valsalva. Thus, she had a primary cesarean delivery. Her postpartum course was only remarkable for improved oxygenation status.
Management of COPA syndrome should be performed by a multidisciplinary team including maternal-fetal medicine, rheumatology, and pulmonology specialists. Traditionally, COPA syndrome is treated with immunomodulator therapy often used to treat autoimmune syndromes. However, many of these medications are not well studied or contraindicated in pregnancy. Preconception counseling is recommended both to ensure pregnancy safe medications being prescribed and to provide information on the genetic inheritance of this disease. At time of entry to care, patients should have a baseline work-up including a radiographic imaging, complete blood count, complete metabolic panel, lactate dehydrogenase, and a 24-hour urine protein collection for baseline. Although thought to be rare, COPA syndrome has an autosomal dominance pattern of inheritance with variable penetrance that is more common in females. Thus, incidence of COPA syndrome in pregnancy will likely increase in the future. Further case studies are warranted to optimize management of patients with COPA syndrome in pregnancy.
COPA综合征是一种罕见的自身免疫性疾病,呈常染色体显性遗传模式,外显率可变,女性发病率高于男性。该疾病在儿童期表现为肺出血、关节炎和肾脏疾病。
我们报告一例20岁未孕患者的产科管理病例,该患者被诊断为COPA综合征。她的病情因多次因低氧血症产前入院以及复杂的物质使用社会心理病史而进一步复杂化。在她第一次产前入院时,风湿病学专家建议根据需要使用羟氯喹、吸入性皮质类固醇(布地奈德)和支气管扩张剂(沙丁胺醇吸入器)进行治疗。在入院引产时,再次发现她存在氧饱和度下降。计算机断层扫描(CT)显示有慢性血栓形成,多学科团队建议避免用力屏气。因此,她接受了剖宫产。她产后的病程仅以氧合状态改善为显著特点。
COPA综合征的管理应由包括母胎医学、风湿病学和肺病学专家在内的多学科团队进行。传统上,COPA综合征采用常用于治疗自身免疫综合征的免疫调节剂疗法进行治疗。然而,这些药物中的许多在孕期并未得到充分研究或存在禁忌。建议进行孕前咨询,以确保开具安全的孕期用药,并提供有关该疾病遗传方式的信息。在开始治疗时,患者应进行基线检查,包括影像学检查、全血细胞计数、全代谢组检查套餐、乳酸脱氢酶检查以及24小时尿蛋白定量检查以确定基线水平。尽管认为COPA综合征罕见,但它具有常染色体显性遗传模式,外显率可变,在女性中更为常见。因此,未来孕期COPA综合征的发病率可能会增加。有必要进行进一步的病例研究,以优化孕期COPA综合征患者的管理。