Department of Radiology, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Department of Surgery, Second Affiliated Hospital of School of Medicine, Zhejiang University, Hangzhou, China.
Medicine (Baltimore). 2023 Dec 22;102(51):e36734. doi: 10.1097/MD.0000000000036734.
Paraesophageal hernias, accounting for a mere 5% to 10% of all hiatal hernias, occasionally present an exceedingly uncommon yet gravely consequential complication characterized by the inversion of the stomach. Delving into the clinical manifestations and optimal therapeutic approaches for patients afflicted by this condition merits substantial exploration.
A 60-year-old man was referred to our hospital with acute onset of severe epigastric pain, abdominal distension, and vomiting. A chest radiograph unveiled an elevated left diaphragmatic dome accompanied by a pronounced rightward shift of the mediastinum. Subsequent abdominal computed tomography imaging delineated the migration of the stomach, spleen, and colon into the left hemithorax, facilitated by a significant diaphragmatic defect.
The diagnosis of a giant paraesophageal hernia with complete gastric inversion was established through a comprehensive evaluation of the patient's clinical manifestations and imaging findings.
Surgical intervention was performed on the patient. During the procedure, a left diaphragmatic defect measuring approximately 10 × 8 cm was identified and meticulously repositioned, followed by the repair of the diaphragmatic hernia. The herniated contents comprised the pancreas, stomach, spleen, a segment of the colon, and a portion of the greater omentum.
The patient experienced a smooth postoperative recuperation and was discharged 12 days following the surgical procedure. Subsequently, during a 7-month follow-up period, the patient continued to exhibit favorable progress and recovery.
Paraesophageal hernias are rare, and the presence of an inverted stomach in a giant paraesophageal hernia is exceptionally uncommon. Clinical presentation lacks distinct features and can lead to misdiagnosis. This case emphasizes the importance of timely surgical intervention guided by imaging, offering valuable clinical insights.
食管裂孔疝占所有食管裂孔疝的 5%至 10%,偶尔会出现一种非常罕见但后果严重的并发症,其特征是胃的反转。深入研究患有这种疾病的患者的临床表现和最佳治疗方法值得深入探讨。
一名 60 岁男性因突发严重上腹痛、腹胀和呕吐而被转至我院。胸部 X 光片显示左膈肌穹顶升高,伴纵隔明显右移。随后的腹部 CT 成像显示胃、脾和结肠迁移到左胸腔,这是由明显的膈肌缺陷促成的。
通过全面评估患者的临床表现和影像学发现,诊断为巨大食管裂孔疝伴完全胃反转。
对患者进行了手术干预。在手术过程中,发现一个大约 10×8cm 的左膈肌缺陷,并进行了精心的复位,随后修复了膈肌疝。疝出的内容物包括胰腺、胃、脾、一段结肠和一部分大网膜。
患者术后恢复顺利,术后 12 天出院。随后,在 7 个月的随访期间,患者继续表现出良好的进展和恢复。
食管裂孔疝很少见,巨大食管裂孔疝中胃的反转更是非常罕见。临床表现缺乏明显特征,可能导致误诊。这个病例强调了在影像学指导下及时进行手术干预的重要性,提供了有价值的临床见解。