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分娩期间的纵隔气肿和心包积气:一例罕见产后现象的报告

Pneumomediastinum and Pericardium During Labour: A Report on a Rare Postpartum Phenomenon.

作者信息

Chen Nelson, Daly Tessa K, Nadaraja Roshini

机构信息

General Surgery, Austin/Northern Hospital, Melbourne, AUS.

General Surgery, Northern Hospital, Melbourne, AUS.

出版信息

Cureus. 2023 Dec 20;15(12):e50850. doi: 10.7759/cureus.50850. eCollection 2023 Dec.

Abstract

Hamman's syndrome (HS) is characterised by spontaneous pneumomediastinum and subcutaneous emphysema. It is a rare phenomenon that can occur during labour. Its incidence is 1 in 100,000 births and predominantly affects young primiparous women with prolonged labour. Patients commonly present with subcutaneous emphysema, chest pain, and dyspnoea. We present the case of a 20-year-old primigravida female with no other medical history who had prolonged labour at 43 weeks gestation. Sudden-onset, right-sided cheek pain and swelling was noted immediately after delivery accompanied by pleuritic chest pain. Chest X-ray (CXR) and computed tomography (CT) demonstrated significant pneumomediastinum and pneumopericardium with subcutaneous emphysema extending to the neck. She was managed symptomatically in addition to antibiotics and discharged after three days with complete resolution of symptoms. No concerns were raised during the follow-up. HS is a rare phenomenon that can occur during labour, particularly in young primiparous females with a prolonged second stage. Radiological investigations in the form of CXR and CT are recommended to rule out life-threatening complications and other conditions that may require immediate management. HS occurs due to rupture of peripheral alveoli secondary to increased intrathoracic pressures from excessive Valsalva manoeuvre allowing air to dissect and enter into the mediastinum. Pneumopericardium in association with HS is extremely rare. It is particularly clinically important because it can cause cardiac tamponade requiring immediate surgical management. HS is otherwise a self-limiting condition and management is symptomatic only. Our case is unique due to the presence of pneumopericardium in association with HS, the fourth ever reported in the literature. Due to its rarity, the incidence of tamponade in this cohort of patients is yet to be delineated.

摘要

哈曼综合征(HS)的特征为自发性纵隔气肿和皮下气肿。它是一种在分娩期间可能出现的罕见现象。其发病率为1/100000活产,主要影响分娩时间延长的初产年轻女性。患者通常表现为皮下气肿、胸痛和呼吸困难。我们报告一例20岁初产妇,无其他病史,妊娠43周时分娩时间延长。产后立即出现突发的右侧脸颊疼痛和肿胀,并伴有胸膜炎性胸痛。胸部X线(CXR)和计算机断层扫描(CT)显示有明显的纵隔气肿和心包积气,皮下气肿延伸至颈部。除使用抗生素外,对其进行了对症处理,三天后症状完全缓解出院。随访期间未出现问题。HS是一种在分娩期间可能出现的罕见现象,尤其是在第二产程延长的初产年轻女性中。建议进行CXR和CT形式的影像学检查,以排除可能需要立即处理的危及生命的并发症和其他情况。HS是由于用力呼气动作过度导致胸腔内压力增加,继发外周肺泡破裂,使空气进入纵隔并扩散所致。与HS相关的心包积气极为罕见。它在临床上尤为重要,因为可导致心脏压塞,需要立即进行手术处理。否则,HS是一种自限性疾病,仅进行对症治疗。我们的病例因合并HS出现心包积气而独特,这是文献中第四例报道。由于其罕见性,该组患者中心脏压塞的发生率尚待明确。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5090/10798797/a20c9fcb730c/cureus-0015-00000050850-i01.jpg

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