Lingegowda Anilkumar Pura, Sushmitha R
Department of Pediatric Surgery, Sakra World Hospital, Bengaluru, Karnataka, India.
J Indian Assoc Pediatr Surg. 2025 Jul-Aug;30(4):541-543. doi: 10.4103/jiaps.jiaps_19_25. Epub 2025 Apr 25.
Pneumoperitoneum, the presence of free air in the peritoneal cavity, is most commonly associated with hollow viscus perforation, necessitating urgent surgical intervention. However, in rare cases, pneumoperitoneum can result from thoracic air leaks and may be managed conservatively unless it is causing diaphragmatic splinting. The aim of the study was to raise awareness about pneumoperitoneum secondary to pneumothorax, emphasizing nonoperative management to prevent unnecessary surgical interventions and associated morbidity. A 1-month-old female infant presented with respiratory distress requiring mechanical ventilation. Following intubation, the child deteriorated clinically, developing significant abdominal distension. Chest X-ray and abdominal X-ray revealed bilateral pneumothorax and pneumoperitoneum. Bilateral intercostal drains (ICDs) were placed, but due to worsening abdominal distension, an exploratory laparotomy was performed within a few hours. No evidence of hollow viscus perforation was found. Tense pneumoperitoneum confirmed with gush of air on opening the abdomen. The presence of air inside the left paracolic gutter extending to the diaphragm indicating it is from pneumothorax. The abdomen was closed with a drain, which was removed after 48 h. Feeds were initiated after 48 h. ICD was removed after 5 days and she was discharged after 7 days. Spontaneous pneumoperitoneum secondary to pneumothorax is an uncommon but important differential diagnosis. Recognizing key clinical clues, such as absence of gastrointestinal symptoms, history of respiratory distress, and extraperitoneal air on imaging, can facilitate conservative management, avoiding unnecessary surgical intervention.
气腹,即腹腔内存在游离气体,最常见于中空脏器穿孔,这需要紧急手术干预。然而,在罕见情况下,气腹可由胸腔漏气导致,除非引起膈肌压迫,否则可采用保守治疗。本研究的目的是提高对气胸继发气腹的认识,强调非手术治疗以防止不必要的手术干预及相关并发症。一名1个月大的女婴因呼吸窘迫需要机械通气。插管后,患儿临床情况恶化,出现明显腹胀。胸部X线和腹部X线检查显示双侧气胸和气腹。放置了双侧肋间引流管(ICD),但由于腹胀加重,数小时内进行了剖腹探查术。未发现中空脏器穿孔的证据。打开腹部时可见大量气体证实存在张力性气腹。左结肠旁沟内的气体延伸至膈肌表明其来自气胸。腹部缝合并留置引流管,48小时后拔除。48小时后开始喂养。5天后拔除ICD,7天后出院。气胸继发的自发性气腹是一种罕见但重要的鉴别诊断。识别关键临床线索,如无胃肠道症状、呼吸窘迫病史以及影像学上的腹膜外气体,有助于保守治疗,避免不必要的手术干预。