Journal of Reproductive Medicine Gynaecology & Obstetrics Category: Medical Type: Case Report

Post-Partum Hamman’s Syndrome: A Case Report and Literature Review

Oliva C1,2*, Mauro R3, Fiorelli C4, Nocita E4,5, Sergi C4,3,5, Bucari D1, Pastore G1, Rosica G1, Ebano V1, Squarcella A1, Tittoni R1Spina V1Ianniello F1Monaco G4,5Dominicis Ade1 and Musella A1

1 Department of obstetrics and gynecology, San Camillo De Lellis Hospital, 02100, Rieti, Italy
2 Unicamillus International Medical University, Rome, Italy
3 Department of Anesthesiology and Intensive Care, San Filippo Neri Hospital, Rome, Italy
4 Department of obstetrics and gynecology, San Filippo Neri Hospital, Rome, Italy
5 Department of obstetrics and gynecology, “Tor Vergata” University, Rome, Italy

*Corresponding Author(s):
Oliva C
Department Of Obstetrics And Gynecology, San Camillo De Lellis Hospital, 02100, Rieti, Italy
Tel:+39 0746278270,

Received Date: Dec 04, 2021
Accepted Date: Dec 10, 2021
Published Date: Dec 17, 2021


Hereby, the case of a low obstetrical risk nulliparous 25-years-old woman, presenting with chest pain and subcutaneous emphysema on face, neck and sternum four hours after spontaneous vaginal delivery has been reported. Early diagnosis of pneumomediastinum through Computed Tomography (CT) scan, clinical and laboratory exams allowed a timely and adequate management without further complications. Differential diagnosis with Hamman’s syndrome has to be taken in mind in case of cough, chest pain, breath difficulty arising after labour and vaginal delivery.


Chest pain; Delivery; Pneumomediastinum; Subcutaneous emphysema


Post-partum spontaneous pneumomediastinum, known as Hamman’s syndrome, was firstly described in 1945 by Louis Hamman [1]. It is defined by a, non-injury-cause, free air presence in the mediastinum and represents a rare complication of second stage of labour with an incidence rate of 1 in 100.000 deliveries [2-11]. Globally, its incidence is approximately 1/25.000 between 5 and 34 years old and the majority of patients (70%) are males [12]. It has been most commonly reported in young nulliparous women. Despite worrying symptoms, the course of this disease is self-limiting [2]. It is usually clinically evident only in the postpartum period even if it occurs from the second stage of labour [10]. Chest pain is the most common symptom of pneumomediastinum, although the severity depends on the location and amount of air. Additional symptoms may include dyspnea, cough and palpitations. Subcutaneous emphysema in the neck has also been linked to vomiting during pregnancy [4]. Excessive Valsalva manoeuvre during vaginal delivery and excessive retching, coughing and straining are frequently reported causes. Pathophysiology of this condition is alveoli’s fissure and infiltration of air through broncho-vascular connective tissue. Eventually subcutaneous emphysema is the result of diffusion of air to subcutaneous tissues [8]. Chest X-ray is a useful early diagnostic technique. We report the case of a twenty-five-year-old woman who was diagnosed with Hamman’s syndrome after her vaginal delivery.

Case Report

A 25-years-old Caucasian woman, nulliparous with unremarkable obstetrical history was admitted to the Department of Obstetrics and Gynecology of San Filippo Neri Hospital at her 41 weeks of gestation because of labour beginning. She was smoker, also during pregnancy, and presented a Body Mass Index (BMI) of 26,7. Her medical history included involvement in a car accident two years before pregnancy resulting in a whiplash injury that was treated with a cervical collar neck for about 2 months. The first stage of labour was uneventful and, as requested from the woman, an epidural catheter for the labour analgesia was placed after anesthesiological evaluation and informed consent signed, without any complications. To encourage the contractions and stabilize them a continuous infusion of oxytocin, with an initial dose of 5 UL in 500 ml of physiological solution at 0,9% at a speed of 3ml/h was started (according to the protocol of our hospital the speed of the infusion gets doubled every 30 minutes). The woman experienced a single episode of sickness in the early hours of the labour. After about five hours from admission the uterine cervical dilation progresses to 4 cm, with subsequent spontaneous amniotic sac rupture and release of clear liquid. Consequently, the continuum infusion of Oxycitin was suspended (up to a 60 ml/h) due to the start of regular and intense contractions. After one hour, a complete cervical dilation was detected. During the second stage of the labour continuous cardiotocographic monitoring was performed and the Foetal Heart Rate (FHR) was always regular. After approximately 2 hours of active pushing, delivery of her baby happened successfully and neither episiotomy nor the Kristeller’s manoeuvre were necessary. The baby was in good general health conditions with a body weight of 4,340 kg and an Apgar score of 9 at 5 mins after birth. 

At 10 pm, four hours after deliver, the woman presented a serious subcutaneous emphysema on her face, neck, collarbones and sternum. A CT scan was immediately performed with detection of pneumomediastinum and no signs of pneumothorax or any other issues on the pulmonary parenchyma were found (Figure 1). The radiological report showed “an abundant presence of a subcutaneous emphysema, with pneumomediastinum. There was an anterolateral irregularity in the wall of trachea, above the carina” (Figure 2). The patient felt a little pain on her chest but hemodynamic and respiratory parameters were always regular. The physical examination was normal except for the presence of a subcutaneous emphysema from her jaw to her sternum. The emergency surgeon and the pneumologist were also consulted and the patient was transferred to the referral pneumological center at Agostino Gemelli Hospital in Rome.

Figure 1: Thoracic computed tomography showing pneumomediastinum and abundant subcutaneous emphysema.

Figure 2: Chest computed tomography showing pneumomediastinum and subcutaneous emphysema and an anterolateral irregularity in the wall of trachea. 

There, the patient was checked for further 24 hours, repeated chest X-ray (Figure 3) and CT scan with no evidence of tracheal rupture but confirming the presence of pneumomediastinum with subcutaneous emphysema. No alterations of Arterial Blood Gas (ABG) analysis were detected. The thoracic surgery team kept the patient under observation, treated her conservatively with analgesia and antibiotics and disposed a next a chest X-ray after seven days of treatment. Subsequently the woman returned to our Hospital, she received multiple pneumological controls and chest CT scan and X-ray were performed once again, revealing pneumomediastinum decrease and subcutaneous emphysema reduction. Eight days after spontaneous delivery, she was discharged home in good general health conditions without other post-partum complications and with scheduled chest X-ray after one month. At one year of follow-up she is healthy and asymptomatic.

Figure 3: Chest X-rays showing pneumomediastinum and subcutaneous emphysema.


Pneumomediastinum associated with pneumothorax and subcutaneous emphysema is a rare obstetric complication. The causal mechanism of Hamman’s syndrome is thought to be due to excessive intrathoracic pressure associated with Valsalva manoeuvre which leads to distal alveolar rupture [13]. Valsava’ s manoeuvre, is a forced expiratory effort against a closed or blocked air passage. Inevitably, it is employed during labour when coughing, vomiting, screaming or pushing and rarely, it causes a break-up of the alveoli and the income of air into the mediastinum [5]. Few cases of pregnancy-related Hamman's have been reported in literature until now [2-9,14-22], with chest pain as most common symptom (85% of patients), followed by crepitus (71%) [23]. Other symptoms include facial or neck swelling, dyspnea, tachycardia and dysphonia [24,25]. Hamman’ syndrome treatment is symptomatic. Chest pain, dyspnoea, anxiety can be treated with oxygen, analgesics and sedatives [5]. Prognosis is generally favourable and the course is self-limited; nevertheless, a prompt diagnosis is basic for an adequate management [2]. Chest X-ray is considered the primary investigation method, however chest CT remains the gold standard for detecting pneumomediastinum [26]. Because of its rarity, no standard management of Hamman’s syndrome or prevention in future pregnancies is still available. Fortunately most of cases are uncomplicated and conservative treatment remains the most appropriate [23]. The differential diagnosis of a Hamman’s syndrome includes amniotic fluid embolism, pulmonary embolism, myocardial infarction, pneumothorax, aortic dissection, Boerhavee’s syndrome, interstitial emphysema, pneumopericardium, cardiac tamponade and mediastinitis [7]. After this experience, considering timing of labour and vaginal delivery, we can assume that nulliparity, a prolonged second stage of labour associated with pushing could be risk factors for pneumomediastinum. This case led us to consider Hamman’ syndrome as differential diagnosis when symptoms as cough, chest pain and difficult breath are reported by the patients during a prolonged second stage of labour or after delivery. Our purpose is to highlight this occurrence in order to raise awareness health professionals of pregnancy-related Hamman’s syndrome and make early diagnosis and timely appropriate management.


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Citation: Oliva C, Mauro R, Fiorelli C, Nocita E, Sergi C, et al. (2021) Post-Partum Hamman’s Syndrome: A Case Report and Literature Review. J Reprod Med Gynecol Obstet 6: 089.

Copyright: © 2021  Oliva C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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