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Ann Thorac Surg 2002;73:1288-1289
© 2002 The Society of Thoracic Surgeons
a Department of Surgery, Division of Cardiothoracic Surgery, Medical College of Virginia, Richmond, Virginia, USA
Accepted for publication July 30, 2001.
* Address reprint requests to Dr DeAnda, West Hospital, 1200 E Broad St, 7th Floor, South Wing, Room 7305, Richmond, VA 23298 USA
e-mail: adeanda{at}nsc1.nsc.vcu.edu
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| Introduction |
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An 88-year-old man was admitted to an outside hospital with a 2-day history of chest pain and shortness of breath. His chest pain worsened with deep breathing, and he reported a productive cough of white-colored sputum. He was without fever, chills, nausea, or vomiting. His past medical history was remarkable for asthma as well as tobacco and alcohol abuse. There was no history of trauma. On his initial physical exam, he was in significant respiratory distress, tachypnic at 40 per minute with diffuse rhonchi and expiratory wheezing. The abdominal exam was unremarkable.
Preliminary laboratory values included hemoglobin of 13 g/dL and a white blood cell count of 19,400 per cc (with 20% bands). The serum electrolytes revealed an anion gap of 30 meq/L with arterial blood gas remarkable for pH 7.17, pCO2 19 mmHg, pO2 69 mmHg. There was no evidence of myocardial ischemia.
A chest roentgenogram revealed marked elevation of the left hemidiaphragm with a concentric stripe of air immediately beneath it, and the splenic flexure and abdominal contents in the region of the left hemithorax. Because of his respiratory status, the patient was intubated and a nasogastric tube placed. A repeat chest film to confirm tube placement showed significant rightward mediastinal shift, the presence of gas bubbles, and the tip of the nasogastric tube in the left hemithorax (Fig 1). An unenhanced computed tomography of the chest, abdomen, and pelvis with oral contrast was then obtained. This revealed multiple small and large bowel loops in the left chest with a resultant right mediastinal shift and possible gastric volvulus (Fig 2).
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| Comment |
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Bochdalek hernia presentation in adulthood is rare with little more than 100 cases reported in the literature [1]. Delayed presentations are more frequent in males by 3:1. A left-sided diaphragmatic defect is present 70% to 90% of the time, thought to arise in part from a differential in the timing of pleuroperitoneal fold fusion between the right and left sides and in part by a protective effect exerted by the liver on the right side. Rarely, hernias present bilaterally or only on the right side [2]. A peritoneal hernia sac is not present in over 85% and also appears dependent on the timing of pleuroperitoneal fold fusion.
Adulthood clinical presentation can be complex with symptomatology generally referable to the aerodigestive tract. Gastrointestinal tract symptoms can include intermittent abdominal pain, vomiting, and dysphagia. Respiratory symptoms usually include chest pain and dyspnea. Delayed and missed diagnosis, as in this case, is a common feature to many presentations and can result in highly morbid and sometimes lethal outcomes [3]. The contents of the Bochdalek hernia may vary depending on the side of the defect. The large and small bowel is most commonly involved [3]. The stomach and omentum are also frequently seen. Herniated contents have also included the liver, gallbladder, spleen, kidney, adrenal gland, and pancreas [4].
A chest roentgenogram demonstrating gas and fluid-filled viscera above the diaphragm can support the diagnosis of Bochdalek hernia. Other more subtle findings include blunting of the costophrenic angle, presence of a posterior mediastinal mass, and small pleural effusion [4]. Computed tomography can also be diagnostic. Typical findings are abutment of fat or soft tissue along the upper surface of the diaphragm, characteristic posterolateral location on the hemidiaphragm, diaphragmatic discontinuity adjacent to the mass, and density continuity above and below the diaphragm through the defect [4]. Intestinal series with gastrograffin or barium have also been used to confirm the diagnosis [4].
Effective treatment involves reducing abdominal contents and repairing the diaphragmatic defect. Transthoracic repair is the usual choice for right-sided Bochdalek hernias, while controversy exists regarding the optimal surgical approach for left-sided hernias. Some support laparotomy and believe this approach is most advantageous for malrotation recognition and treatment [5]. Thoracotomy advocates cite an improved ability to divide chronically formed adhesions between abdominal viscera and thoracic structures [3]. However, both approaches may prove equally suitable. More recently, both laparoscopic and thoracoscopic techniques have been successfully utilized in repair of these rare hernias [6].
In summary, Bochdalek-type congenital diaphragmatic hernia can present in the adult or even geriatric population. Outcome of adult patients having Bochdalek hernia depends on the type of clinical presentation. The mortality rate for elective surgery has been reported at less than 3% [5]. However, mortality can be as high as 32% when patients present acutely, when diagnosis is delayed (as in this case) or complications develop [5]. A high index of suspicion can result in early diagnosis and prompt intervention with reduced morbidity and mortality.
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This article has been cited by other articles:
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G. Dalencourt and M. R. Katlic Abdominal Compartment Syndrome After Late Repair of Bochdalek Hernia Ann. Thorac. Surg., August 1, 2006; 82(2): 721 - 722. [Abstract] [Full Text] [PDF] |
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Y. Chai, G. Zhang, and G. Shen Adult Bochdalek hernia complicated with a perforated colon J. Thorac. Cardiovasc. Surg., December 1, 2005; 130(6): 1729 - 1730. [Full Text] [PDF] |
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