Anesthetic experience of a patient with Prune-belly syndrome

provided the original work is properly cited. CC Prune-belly syndrome is a rare congenital disease (1 : 35,000– 1 : 50,000) with characteristic abdominal folds that have a driedplum appearance, and the most typical triad is abdominal muscle deficiency, urinary tract abnormality, and cryptorchidism [1-4]. Other than the triad, there could be accompanying cardiovascular, musculoskeletal, gastrointestinal, respiratory, and central nerve system abnormalities in 75% of patients [2]. Due to such abnormalities, many of the patients may need diagnostic or therapeutic procedures from infancy, and general anesthesia may be required in performing procedures or operations. Patients can encounter many problems internally and surgically during anesthesia due to anatomical deficiency. Herein, the authors experienced a case in which a patient with prune-belly syndrome received anesthesia, and together with a literature review, we report several characteristics for prune-belly syndrome which anesthesiologists should take precautions for when administering anesthesia. An 8-year-old boy weighing 20 kg visited the hospital for permanent catheter attachment and formulation of an A-V fistula for hemodialysis. The patient had been diagnosed with prunebelly syndrome at birth and received an abdominoplasty when he was 3 years old. He also had a history of receiving stereotactic hematoma evacuation and closed drainage due to spontaneous intracranial hemorrhage and intraventricular hemorrhage caused by hypertension when he was 7 years old. At the time of hospitalization, the patient underwent hemodialysis three times a week for chronic renal failure and received treatment for hypertension which could not be managed well. During the hospitalization, the existing permanent catheter in the subclavian vein was removed and a femoral catheter was temporarily attached to the maintain hemodialysis. Prune-belly patients can have accompanying renal dysfunction or renal failure from obstructive uropathy or kidney dysplasia, so renal function should be evaluated before anesthesia through BUN, creatinine, and creatinine clearance figures. In addition, any anesthesia should be carefully planned to prevent deterioration of renal function or renal failure after surgery. The patient in this case was already receiving hemodialysis treatment for chronic renal failure, so hemodialysis was to be done the day before and after the surgery. There were no problems in mouth opening or neck extension, but intubation was expected to be difficult because the patient had a small jaw and a large tongue. Due to oligohydramnios, prune-belly patients can exhibit Potter’s face with micrognathia, flattened nose, and malformed ears [1,5]. Before anesthesia, there should be preparation for circumstances where maintaining an airway is difficult through physical examination to observe symptoms of facial malformations. In addition, vomiting and regurgitation can occur frequently in prune-belly patients with uremia, so particular attention should be needed when inducing anesthesia or awakening. The patient showed great agitation before entering the operating room so 1 mg of midazolam was IV injected twice. After preoxygenation, anesthesia was induced with propofol 50 mg, fentanyl 20 μg, and rocuronium 10 mg. Manual ventilation was maintained for approximately 1 minute, and then, intubation was performed with a cuffed endotracheal tube with a 5.5 mm diameter. The vocal cord could be observed easily, and intubation was performed well. However, it was observed very large tongue and too small epiglottis. If vomiting occurs during anesthesia in such patients, aspiration can occur more easily than in average children, and it will be very difficult to maintain an