• Journal of Chest Surgery
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• v.6 no.1
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• pp.57-62
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• 1973

Pericardial cyst and diverticula are not uncommon. Rarely do they cause symptoms and the diag-nosis has been made primarily at operation. In Korea, there is no reported case of pericardial coelomic cyst, and one case of pericardial coelomic cyst, middle aged female with symptoms of general malaise, weight loss and mild discomfort on her anterior chest, is presented with related references. Pathological diagnosis after removal of the mass revealed pericardial coelomic cyst.

• Journal of Chest Surgery
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• v.28 no.9
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• pp.865-868
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• 1995

A case of bronchogenic cyst associated with a partial pericardial defect is reported. Bronchogenic cysts are not so rare in incidence, but they are more rare when associated with a pericardial defect, the first case being reported by Rusby and Sellors in 1945. Recently, we experienced such a rare case of a bronchogenic cyst with a partial pericardial defect. The patient is a 39-year-old female and she was found to have a left anterior mediastinal mass during routine chest X-ray. During the operation, we detected partial pericardial defect after removal of the mediastinal mass. The pericardial defect was repaired with a Gore-Tex Membrane. The pathological examination of the mass showed a bronchogenic cyst. The patient had an uneventful hospital course.

• Journal of Chest Surgery
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• v.42 no.6
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• pp.781-784
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• 2009

Pericardial cyst is an uncommon congenital mediastinal tumor. The majority of pericardial cysts are located in the right cardiophrenic angle, but rarely they can be located intrapericardially. We now present a case of a huge intra-pericardial pericardial cyst excised with video-assisted thoracoscopic surgery.

• Journal of Chest Surgery
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• v.20 no.2
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• pp.353-357
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• 1987

We recently experienced a case of bronchogenic cyst associated with situs inversus and partial pericardial defect. The patient was 26-day-old-male who showed severe respiratory difficulty. Left upper lobectomy and direct suture of partial pericardial defect were undergone successfully, but his postoperative course was unfortunate because of respiratory insufficiency.

• Journal of Chest Surgery
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• v.17 no.2
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• pp.321-325
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• 1984

Bronchogenic cyst and pericardial diverticulum are relatively infrequent respectively, but they have been detected more commonly with the increasing popularity of the routine and mass survey examination of the chest. A 31 year-old male was admitted for the evaluation of productive cough and two mass lesions in left side on the chest films and bronchogram. Exploratory thoractomy revealed pericardial diverticulum and bronchogenic cyst, which were confirmed by pathologic examination. We are willing to report this combined case which was treated uneventfully by left lower lobectomy and diverticulectomy.

• Journal of Chest Surgery
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• v.16 no.1
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• pp.167-170
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• 1983

Pericardial cysts are infrequent benign intrathoracic lesions. They rarely cause symptoms, and they are usually discovered on routine X-ray by chance. Over 70% of the cases occur at the right anterior cardiophrenic angle. Surgery is generally not indicated if the diagnosis of pericardial cyst can be made with certainty, and then an operation is performed to rule out other lesions. The authors present 3 cases of pericardial cyst confirmed by surgery. In two Gases Of the three, the pericardial cysts were located at the right anterior cardiophrenic angle, and in one case, at the left superior area of the posterior mediastinum. We managed them successfully by surgery, and they were discharged uneventfully.

• Journal of Chest Surgery
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• v.51 no.1
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• pp.72-75
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• 2018

Pericardial cysts are rare benign anomalies generally discovered as incidental findings on radiographic images. Rarely, pericardial cysts cause symptoms and may lead to complications. A 56-year-old woman presented to the emergency department for mild chest pain. A cardiovascular and respiratory examination revealed no abnormalities, while a chest X-ray and subsequent thoracic computed tomography (CT) showed a pericardial cyst. The patient refused both percutaneous treatment and thoracic surgery. Three years later, a thoracic CT scan showed that the pericardial cyst had disappeared. Although the spontaneous resolution of these lesions is rare, this article highlights the possibility of conservative management in select cases.

• Journal of Chest Surgery
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• v.46 no.2
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• pp.138-141
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• 2013

Pericardial cysts are reported by some authors, but epicardial cysts are extremely rare. We report one case of epicardial cyst that was detected incidentally and was removed successfully. Furthermore, unusually, pathological examinations confirmed that the cyst wall was looked like a vessel wall.

• Journal of Chest Surgery
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• v.40 no.6 s.275
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• pp.459-462
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• 2007

Pericardial cysts are uncommon benign congenital mediastinal lesions and they are most often found in either cardiophrenic angle. We present here one case of atypically located pericardial cyst that was located in the sub-pulmonary region. The clinicians should take into consideration this entity in the differential diagnosis of cystic lesion of the mediastinum. The diagnostic difficulties that are encountered and the utility of video-assisted thoracoscopy are described.

• Journal of Chest Surgery
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• v.56 no.4
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• pp.286-289
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• 2023

A 58-year-old woman presented with an incidental asymptomatic mass occupying the entire right lower thorax. A radiologic study demonstrated a huge cystic mass, initially suggestive of an exophytic echinococcal cyst. After unsuccessful catheter drainage, the patient was referred for surgery, and curative resection of the lung-, heart-, and diaphragm-compressing mass was performed under video-assisted thoracoscopic surgery. Culture studies revealed no growth of parasitic, bacterial, or fungal infections, and the final pathological result confirmed a primary pleural cyst. Thoracic cystic masses mostly manifest as bronchogenic or pericardial cysts, while primary pleural cysts have rarely been reported. We present a rare case of a huge pleural cyst that initially mimicked an echinococcal cyst.