• Journal of Chest Surgery
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• 제24권8호
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• pp.830-835
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• 1991

Tuberculosis is a chronic disease caused by Mycobacterium tuberculosis, which usually affects the lung but may cause lesions in any organ or tissue of the human body. Mediastinal lymph node involvement is common feature of intrathoracic tuberculosis in children. Sometimes the lymph node may be enlarged and it causes compressive symptoms. Recently we experienced two cases of tuberculous abscess at middle mediastinum. The abscess seemed to be originated from the mediastinal lymphadenitis, and caused the symptoms. Operation was performed by median sternotomy and by posterolateral thoracotomy incision respectively for the purpose of relieving symptoms and diagnosing the mediastinal mass. The symptoms were relieved completely and postoperative course was uneventful.

• Journal of Chest Surgery
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• 제25권8호
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• pp.795-799
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• 1992

The Mediastinal lipoma is an uncommon tumor in the literature. The literaure concerning mediastinal lipomas began with the first case report by Fothergill in 1781 and about 120 cases had been reported till 1969. We experienced one case of huge mediastinal lipoma, which was 885gm in weight, The mass was successfully removed through the right posterolateral thoracotomy and pathologic report confirmed pure adipose tissure. The patient`s postoperative course was uneventful and he was discharged on the 17th day.

• Tuberculosis and Respiratory Diseases
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• 제40권6호
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• pp.747-750
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• 1993

A 51-year-old male was admitted due to mediastinal mass. Chest PA showed a $4{\times}5$ cm sized round mass on right lower paratracheal area. The chest computerized tomogram showed cystic mass located between superior vena cava and trachea. This cystic mass was composed of variable internal architecture with Hounsfield unit(HU) from -44.4 to +25.5. The resected cystic mass revealed ectodermal, mesodermal, and endodermal structures. We report a case of anterior mediastinal cystic teratoma confirmed by open thoracotomy.

• Journal of Chest Surgery
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• 제4권2호
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• pp.87-90
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• 1971

The mediastinal lipoma is an extremely rare tumor in children. Since the orininal description by Fothergill in 1781, about 120 cases have been reported in the world literature. Of these, less than 10 have been reported in children below the age of 12. We had experienced a posterior mediastinal lipoma in 3 year old boy. He did not complain of any subjective symptoms. Routine X-ray film revealed a huge round homogenous mass density in the posterior mediastinum. On posterior thoracotomy incision,bright yellow,well encapsulated, partly 1obular adipose mass was found in the posterior mediastinum. The tumor mass was removed easily,being proved to be lipoma on histopathologic examination. His postoperative course was uneventful and discharged on the 12th postoperative day.

• Journal of Chest Surgery
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• 제7권1호
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• pp.117-122
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• 1974

The benign tumor of smooth muscle, the leiomyoma, may arise anywhere in the body, in such tissues as the muscularis of the gut and the media of blood vessels, although by far its most common location is the uterus. Indeed, the mediastinal leiomyomas are extremely rare, especially when one excludes those arising in the esophagus. No dogmatic statements can be made with regard to age, sex distribution, symptoms, or clinical course because of the extreme paucity of cases available for evaluation. Although the majority of the reported cases are in the posterior mediastinum, thus suggesting esophageal origin. We have experienced a right inferior mediastinal leiomyoma in 36 years old housewife. She complained hemoptysis and right lower chest pain associated with intermittent low-graded fever and chillness. Routine X-ray film revealed a large irregular cystic mass density in the right lower thoracic cavity. On exploratory thoracotomy, a huge round yellow-gray colored solid mass, measured about 2.5kg in weight, was located in the right inferior mediastinum just above right hemidiaphragm, medially. The tumor mass was removed, being proved to be leiomyoma on histopathologic examination. Her postoperative course was uneventful and discharged without complication.

• Journal of Chest Surgery
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• 제40권12호
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• pp.878-881
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• 2007

흉강경적 종격동 종양 절제 후 발생하는 뇌공기증은 매우 드문 합병증으로, 척수근 주위 경막의 손상으로 인해 발생한 거미막하강-흉강 누공이 그 원인이다. 후종격동 종양으로 흉강경적 종양 절제술을 시행 받은 60세 환자가 수술 직후부터 지속적인 오심과 두통을 호소하여 시행한 뇌 전산화 단층 촬영에서 뇌공기증이 진단되었고, 보존적 치료로 호전되었기에 이를 보고하는 바이다.

• Journal of Chest Surgery
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• 제42권4호
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• pp.537-539
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• 2009

47세 여자 환자가 이전부터 있던 흉골상 절흔부에 종괴를 제거하기 위해 내원하였다. 흉부 CT에서 종괴는 상전종격동에 위치하고 있었다. 경부 절개 후에 종괴를 제거하였고 병리학적 검사상 종괴는 결절성 과형성(nodular hyperplasia)을 함유한 이소성 갑상선 조직으로 진단되었다. 저자들은 드문 종격동 이소성 값상선 조직을 치험하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제31권1호
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• pp.69-72
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• 1998

종격동에 발생하는 혈관종은 매우 드문 질환으로 국내외적으로 발표된 예가 흔하지 않다. 본 인제대학교 상계백병원에서는 상대 정맥의 우심방 유입구 상방에 발생한 해면상 혈관종을 수술적 치험하였기에 보고하는 바이다. 환자는 35세된 여자 환자로써 우측 경부의 낭종성 종괴를 주소로 이비인후과 외래를 방문하여 수술을 위해 촬영한 단순 흉부 방사선상 우측 종격동에 비정상적인 음영이 관찰되어 본과로 전원되어 추가 검사 후 수술적 절제를 시행하였다. 절제한 종괴는 상대 정맥의 우심방 유입구 약 2cm 상방에 약 4x5cm 크기의 해면상 혈관종으로 확진되었으며 수술 후 7일째 퇴원하여 현재 외래 통한 관찰 중인 바, 이상 소견 없이 잘 지내고 있다.

• Tuberculosis and Respiratory Diseases
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• 제60권6호
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• pp.684-689
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• 2006

저자들은 심한 호흡곤란으로 내원한 환자에서 원발병소의 재발 및 국소전이 없이 원격전이인 거대한 앞종격동 종괴로 발현된 재발된 자궁경부암의 드문 예를 경험하였기에 보고하는 바이다.

• Korean Journal of Radiology
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• 제22권1호
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• pp.139-154
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• 2021

Magnetic resonance imaging (MRI) has become a crucial tool for evaluating mediastinal masses considering that several lesions that appear indeterminate on computed tomography and radiography can be differentiated on MRI. Using a three-compartment model to localize the mass and employing a basic knowledge of MRI, radiologists can easily diagnose mediastinal masses. Here, we review the use of MRI in evaluating mediastinal masses and present the images of various mediastinal masses categorized using the International Thymic Malignancy Interest Group's three-compartment classification system. These masses include thymic hyperplasia, thymic cyst, pericardial cyst, thymoma, mediastinal hemangioma, lymphoma, mature teratoma, bronchogenic cyst, esophageal duplication cyst, mediastinal thyroid carcinoma originating from ectopic thyroid tissue, mediastinal liposarcoma, mediastinal pancreatic pseudocyst, neurogenic tumor, meningocele, and plasmacytoma.