• Journal of Chest Surgery
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• 제27권9호
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• pp.812-814
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• 1994

The esophageal cyst result from a wrong cleavage of the primitive gut in the 4 weeks embryo. In embryo and after seperation of the tracheal diverticulum, the esophagus is lined with ciliated cells which are able cover a "cystic duplication". It is often difficult to distinguish between the bronchogenic and the esophageal cyst. Pathological findings showed the presence of a ciliated epithelium without cartilage which was diagnosed as an esophageal cyst. The patient was 21 year old man for evaluation of the cyst in the posterior mediastinum. The cyst was located the intramural esophagus. Microscopically, the cyst was lined with ciliated columnar epithelium and there was no evidence of cartilage. The cyst was confirmed as the intramural esophageal cyst.geal cyst.

• Journal of Chest Surgery
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• 제56권4호
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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.

• 한국임상수의학회:학술대회논문집
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• 한국임상수의학회 2009년도 추계학술대회
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• pp.256-256
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• 2009

• Tuberculosis and Respiratory Diseases
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• 제57권6호
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• pp.584-588
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• 2004

수년간의 반복되는 객혈로 내원한 21세 여자환자에서 방사선학적 소견상 진균덩이가 의심되어 흉강경을 이용한 우하엽 절제술을 시행하였으며, 절제한 조직의 병리 조직학적 검사상 기관지 기원 낭내 발생한 국균종과 이에 동반된 방선균증으로 진단된 예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제43권1호
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• pp.120-123
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• 2010

기관지성 낭종은 종격동 내에 비교적 흔히 발생하는 선천성 병변으로 대부분 최소침습적인 방법으로 안전하고 효과적으로 치료할 수 있다. 제한적으로 일부 기관지성 낭종의 경우 발생 위치에 따라 종격 동경을 이용하여 부분 혹은 완전 절제술이 가능하다. 저자들은 좌측 하방의 기관주위에 위치하는 기관지성 낭종을 비디오 종격동경을 이용하여 완전 절제 치험하였기에 보고하며, 기술적인 면에서 고찰해 보고자 한다.

• 대한기관식도과학회지
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• 제14권1호
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• pp.54-58
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• 2008

Bronchogenic cysts are rare congenital anomalies of the tracheobronchial tree. Most cases present within the mediastinum or pulmonary parenchyma without a patent connection to the tracheobronchial tree or digestive tract in the pediatric age group. Cervical bronchogenic cysts in adults are rare. In this report, we describe two cases of incidentally found paratracheal bronchogenic cysts that presented as asymptomatic neck masses in a 66-year-old female with papillary thyroid carcinoma and in a 59-year-old male of Catleman's disease.

• Journal of Chest Surgery
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• 제28권7호
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• pp.693-697
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• 1995

Intrathoracic cyst was considered rare entity but one of the important diseases in the field of thoracic surgery. Authors had experienced 17 cases of intrathoracic cysts that were treated in the department of thoracic and cardiovascular surgery of Pusan NationalUniversity Hospital for 10years from January, 1983. to December,1992. The summary is as follows: Their age distribution was from 2 years and 9 months to 59 years of age, mean age 27.2 years. There were 8 males and 9 females. The type of intrathoracic cyst was 10 cases of Bronchogenic cyst, 2 cases of Pericardial cyst and 4 cases of Non specific cyst. The anatomical locations of intrathoracic cysts were 6 cases of anterior mediastinum, 2 cases of middle mediastinum, 3 cases of posterior mediastinum and 6 cases of lung parenchyme. The most common symptom was coughing and followed by general weakness, fatigue, chest pain & discomfort and hemoptysis and 6 patients were asyptomatic. The successful complete removal was done at all cases.Postoperative complications were developed in 5 patients but there was no case of hospital mortality.

• Journal of Chest Surgery
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• 제24권2호
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• pp.222-226
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• 1991

Authors recently experienced a case of traumatic pulmonary pseudocyst in 4 year-old girl. Traumatic pulmonary cyst is a rare complication of blunt thoracic trauma, simulating surgical conditions such as lung abscess, localized empyema, or congenital bronchogenic cyst. Unless infection is supervened, surgery is not indicated because of its spontaneous regression. In this article, authors present the case and review the traumatic pulmonary pseudocyst with related articles.

• Journal of Chest Surgery
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• 제11권3호
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• pp.246-252
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• 1978

A three year and seven month old girl with moderate depression deformity of the sternum associated with a huge well defined homogenous hazy mass density of the upper half of the right hemithorax on plain chest x-ray had developed, exertionaI dyspnea (Figs1, 2 and 3). Correction of the funnel chest was carried out with modified Ravitch procedure and resection of the intrathoracic cystic mass was performed through an anterolateral thoracotomy incision in one stage operation satisfactorily (Figs. 7 and 8). On exploration, the mass, $15{\times}12{\times}10$cm in size, was connected to the bronchus at 1cm a bove the carina by a stalk (Fig. 4). The outer surface showed abundant vasculature. The specimen was filled with mucoid material; the inner surface was much trabeculated. glistening and smooth (Fig. 5 and 6). yficroscopically, the cyst was lined with simple or pseudostratified ciliated columnar epithelium. The cystic wall was composed of loose fibrous connective tissue, muscle layers, cartilages with some lymphocytic infiltration (Fig. 9). Isolated cases of funnel chest deformity and congenital bronchogenic cystic disease are not uncommon; however, the assocbtion of the two conditions is yery rare. Therefore. report and review of the literature was done.

• Journal of Chest Surgery
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• 제8권1호
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• pp.13-18
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• 1975

Developmental pulmonary abnormalities are known as rare condition. diagnosis was made at autopsy in the early cases reported, however, as diagnostic aids such as X-ray, bronchography, bronchoscopy and exploratory thoracotomy have come into use, the condition is being discovered more often recently in living persons, and it appears to occur with sufficient frequency to merit consideration in the differential diagnosis of certain chest conditions. According to Schneider and Boyden there are three main types of this abnormality: [1] Agenesis, in which there is complete absence of one or both lungs; there is no trace of bronchial or vascular supply or of parenchymal tissue. [2] Aplasia, in which there is suppression of all but a rudimentary bronchus which ends in a blind pouch; there are no vessels or parenchyma. [3] Hypoplasia, in which the bronchus is fully formed but is reduced in size and ends in a _ flesh structure which usually lies within the mediastinum. Rudimentary pulmonary parenchyma may be present around the bronchial stump and often is the site of cystic malformation. We experienced one case of hypoplastic lung with cystic malformation which was originated from a small aberrant rudimentary bronchus, and the rudimentary bronchus was branched from the right side of tracheal end. The diagnosis was finally confirmed by the histopathological finding. Now, we report this case with a brief review of literatures.