Management of a Novel Autoimmune Disease, COPA Syndrome, in Pregnancy

IF 0.6 Q4 OBSTETRICS & GYNECOLOGY
Archana Ayyar, Rachel D. Seaman, K. Guntupalli, M. Tolcher
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引用次数: 0

Abstract

Background 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. Case 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. Conclusion 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.
妊娠期一种新型自身免疫性疾病COPA综合征的管理
COPA综合征是一种罕见的自身免疫性疾病,表现为常染色体显性遗传模式,具有可变渗透,女性比男性更常见。这种疾病在儿童时期表现为肺出血、关节炎和肾脏疾病。我们提出一个病例的产科管理的20岁无阴道患者的诊断为COPA综合征。她的病例因产前多次因低氧血症入院和复杂的药物使用心理社会史而进一步复杂化。在她第一次产前入院时,风湿病学建议根据需要使用羟氯喹、吸入皮质类固醇(布地奈德)和支气管扩张剂(沙丁胺醇吸入器)。入院引产时,她再次发现氧饱和度过低。在计算机断层扫描(CT)上发现慢性血栓,建议多学科团队治疗Valsalva。因此,她进行了一次剖宫产。她的产后过程只有显著改善氧合状态。结论COPA综合征的治疗应由母胎医学、风湿病学和肺病学专家组成的多学科团队进行。传统上,COPA综合征是用免疫调节剂治疗,通常用于治疗自身免疫性综合征。然而,这些药物中的许多都没有得到很好的研究或在怀孕时禁用。建议孕前咨询,以确保怀孕安全的药物处方,并提供有关这种疾病的遗传信息。在入院治疗时,患者应进行基线检查,包括放射成像、全血细胞计数、全代谢组、乳酸脱氢酶和24小时基线尿蛋白收集。虽然被认为是罕见的,但COPA综合征具有常染色体显性遗传模式,具有可变外显率,在女性中更为常见。因此,未来妊娠期COPA综合征的发生率可能会增加。需要进一步的病例研究来优化妊娠期COPA综合征患者的管理。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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