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Ann Thorac Surg 1999;68:1857-1858
© 1999 The Society of Thoracic Surgeons
a Division of Thoracic Oncology, National Cancer Center Hospital East, Kashiwa, Chiba, Japan
Address reprint requests to Dr Suzuki, Division of Thoracic Surgery, National Cancer Center Hospital, 5-5-1, Tsukiji, Chuoku, Tokyo 104-0045 Japan
e-mail: kjsuzuki{at}ncc.go.jp
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| Introduction |
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A coin lesion was visible in an annual chest roentgenogram of a 69-year-old woman. The patient was a housewife, lived in a rural area, and had never been a smoker. Hypertension was noted as her past history. The right lung tumor was ill-defined, noncalcified, and measured 2.4 by 2.4 cm on the plain x-ray film. Transbronchial biopsy specimen showed a well-differentiated adenocarcinoma. Preoperative workup resulted in a diagnosis of stage IA disease. She underwent right upper lobectomy and systematic mediastinal lymph node dissection on June 26, 1998. Pathologic study of the resected specimen showed a moderately differentiated adenocarcinoma of 3.3 cm in maximum tumor dimension, without metastasis to the locoregional lymph nodes. On the second postoperative day, approximately 300 mL of white turbid fluid was drained through the chest tube, and a postoperative chylothorax was diagnosed. As the chylothorax did not resolve despite a 1-week fast and total parenteral nutrition, 5 KE of OK-432 was administered into the thoracic cavity. Turbid drainage diminished and the chest tube was removed on the 14th postoperative day. Pleural effusion did not accumulate thereafter and the patient was discharged on the 19th postoperative day.
When she visited our outpatient clinic on the 59th postoperative day, a mass in the upper mediastinum was noted on the plain chest roentgenogram. Although the patient remained asymptomatic except slight dyspnea, the size of the mediastinal mass gradually increased. Chest computed tomographic scan on August 30, 1998, showed a low density cystic mass surrounded by a thick and contrast-enhanced capsule in the upper mediastinum (Fig 1). The mass compressed the superior vena cava and trachea. Considering the previous chylothorax, the mass was suspected to be a secondary mediastinal chyloma. As the patient had slight dyspnea and the size of the mass gradually increased, we performed surgical intervention on September 30, 1998. A right thoracotomy revealed a small amount of milky effusion in the thoracic cavity and an elastic mass measuring 5 cm in the upper mediastinum, dorsal to the superior vena cava and ventral to the trachea. The thick capsule was incised and chile spilled out. After the chile was removed, we ligated the thoracic duct immediately cephalad to the diaphragm. The postoperative course was uneventful and the patient was free of any symptoms. The patient was discharged 9 days after the second operation. She is healthy with no signs of mediastinal mass 1 month after operation.
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Mediastinal chyloma developed after a major lung resection and systematic lymph node dissection was reported. This complication is rare; however, it should be noted that it can develop after chemical pleurodesis for chylothorax and compress the major vessels or trachea. Plain chest roentgenogram and thoracic computed tomographic scan were useful in the diagnosis. When necessary, surgical drainage and thoracic duct ligation could successfully manage this complication.
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