Newton Devon H, Betit Alexandria L, Patel Roshni B, DiValentin Louis
Medical Student, Alabama College of Osteopathic Medicine, Dothan, USA.
Internal Medicine, Regional Medical Center, Anniston, USA.
Cureus. 2024 Sep 4;16(9):e68641. doi: 10.7759/cureus.68641. eCollection 2024 Sep.
Hereditary angioedema (HAE) is a rare disorder that causes episodes of angioedema due to a mutation in the C1 esterase inhibitor gene (C1-INH). Complications of HAE include intestinal obstruction, asphyxiation, and venous thromboembolism (VTE). In this case, we report a 34-year-old G4P2011 female with HAE at 24 weeks gestation presenting with acute right upper extremity pain and swelling following a peripherally inserted central catheter (PICC) line for HAE treatment infusion, revealing a right upper extremity VTE. Early treatment with Lovenox, PICC line removal, and continuation of HAE therapy via peripheral IV infusion resolved and prevented further angioedema and subsequent VTEs during this patient's pregnancy. This case serves as an example of effective management of HAE complications during pregnancy and supports peripheral IV line usage over PICC lines for medication infusions in pregnant patients with HAE. The overall purpose of this case report is to improve safety outcomes for pregnant patients with HAE by mitigating the risks of PICC line usage and to highlight the significance of VTE inclusion within the differential diagnosis in this population.
遗传性血管性水肿(HAE)是一种罕见的疾病,由于C1酯酶抑制剂基因(C1-INH)突变导致血管性水肿发作。HAE的并发症包括肠梗阻、窒息和静脉血栓栓塞(VTE)。在本病例中,我们报告了一名34岁、孕4产2011的女性,在妊娠24周时患有HAE,在经外周静脉穿刺中心静脉置管(PICC)进行HAE治疗输液后,出现急性右上臂疼痛和肿胀,检查发现右上臂VTE。使用速碧林进行早期治疗、拔除PICC导管,并通过外周静脉输液继续进行HAE治疗,使症状得到缓解,并防止了该患者在孕期出现进一步的血管性水肿和随后的VTE。本病例是孕期HAE并发症有效管理的一个实例,并支持在患有HAE的孕妇中,使用外周静脉输液而非PICC导管进行药物输注。本病例报告的总体目的是通过降低使用PICC导管的风险,改善患有HAE的孕妇的安全结局,并强调在该人群的鉴别诊断中纳入VTE的重要性。