Maharajh Sandeep, Pilkington James, Almerie Qutayba, Goldsmith Paul
General Surgery, Manchester University NHS Foundation Trust, Manchester, GBR.
Cureus. 2024 Sep 25;16(9):e70152. doi: 10.7759/cureus.70152. eCollection 2024 Sep.
Diaphragmatic hernias have classically been reported due to congenital birth defects and blunt or penetrating trauma. We present a rare case of an intrapericardial diaphragmatic hernia after left-sided pericardial window surgery for chronic pericardial effusions. A 59-year-old female with a background of systemic lupus erythematosus and recurrent pericardial effusions underwent subxiphoid placement of a pericardial-peritoneal window. Postoperatively, she reported exertional shortness of breath. Imaging revealed a diaphragmatic hernia in the pericardial cavity. Open adhesiolysis between the abdominal organs and the heart was performed via a thoracoabdominal approach followed by suture and mesh repair of the defect. The postoperative course was uneventful. Pericardial hernias are rare, with few published cases. Their etiologies can be traumatic, iatrogenic, or congenital, with variable, non-specific symptoms that may occur at any time after the inciting event. With the potential for significant cardiac compromise, clinicians should be aware of this rare diagnosis, and surgical repair must be prioritized. This case documents the successful surgical management of this rare complication. Careful multidisciplinary planning is essential for surgical repair and should be tailored to patient-specific factors.
传统上,膈疝被认为是由先天性出生缺陷以及钝性或穿透性创伤引起的。我们报告了一例罕见的病例,一名患有慢性心包积液的患者在接受左侧心包开窗手术后发生了心包内膈疝。一名59岁女性,有系统性红斑狼疮病史且反复出现心包积液,接受了剑突下心包 - 腹膜开窗术。术后,她诉说活动后气短。影像学检查发现心包腔内有膈疝。通过胸腹联合入路对腹部器官与心脏之间进行开放性粘连松解,随后对缺损进行缝合和网状修补。术后过程顺利。心包疝很少见,发表的病例也很少。其病因可能是创伤性、医源性或先天性的,症状多变且不具特异性,可在诱发事件后的任何时间出现。鉴于其有导致严重心脏功能受损的可能性,临床医生应了解这种罕见的诊断,并且必须优先考虑手术修复。本病例记录了这种罕见并发症的成功手术治疗。仔细的多学科规划对于手术修复至关重要,应根据患者的具体因素进行调整。