• 제목/요약/키워드: Case Review

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흉부 외상 후 발생한 가성 폐낭종: 치험1례 (Traumatic Pulmonary Pseudocyst - A case report -)

  • 전예지;한동기;곽영태
    • 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.

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해면양 임파관종 치험 1예 (Cavernous Hemangioma: one case report)

  • 성시찬
    • Journal of Chest Surgery
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    • 제12권4호
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    • pp.379-382
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    • 1979
  • Cavernous lymphangioma is a benign tumor of lymphatic origin encountering most frequently in young children, and composed of softly fluctuated monolocular or multilocular cystic masses which developed from embryonic outpouching of the venous system. The prevailing site of this tumor Is at the anterolateral neck region particularly posterior triangle, and occasionally axillary, mesentery and spleen etc. Recently, we have experienced one case of left axillary cavernous lymphangioma, which surgically removed successfully and confirmed histopathologically. We want to report one case of left axillary large cavernous lymphangioma with a brief review of the relevant literatures.

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식도와 연결된 선천성 기관지성 낭종의 치험 1례 보 (Bronchogenic cyst communicating with esophagus: report of a case)

  • 이철주;최원희;하정옥
    • Journal of Chest Surgery
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    • 제17권3호
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    • pp.505-510
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    • 1984
  • Among varieties of the mediastinal tumors, benign developmental cysts [Entergenous cysts] occur about 10% of them. From the primitive foregut, tracheobronchial tree and esophagus develop at 3 weeks of its embryonal age, and bronchogenic cyst arises from accessory or supernumerary lung bud. Usually it remains isolated with surrounding structures, and causes no specific symptoms. But few cases of bronchogenic cysts have fistulous communication with esophagus causing compressive symptoms. We report a case of unusual complicated case of bronchogenic cyst with review of literatures.

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폐아세포종 -수술치험 1례- (Pulmonary Blastoma -A Case Report-)

  • 금동윤
    • Journal of Chest Surgery
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    • 제27권10호
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    • pp.868-873
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    • 1994
  • We experienced a very rare case of pulmonary blastoma in a 29 year old female. She complained of left chest pain and dyspnea for 1 month. The characteristic feature of this tumor is it`s biphasic pattern consisting of a spindle cell stroma containing glandular structures. A serial check of simple chest X-ray and computed tomography revealed a growing huge lung mass occupying whole left thorax. We successfully removed the upper lobe of left lung with a huge tumor mass. Pathologic study revealed this tumor as pulmonary blastoma. We report a case with review of literature.

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기관절개 및 비내시경을 이용하여 치험한 기관이물 1례 (A CASE OF BRONCHIAL FOREIGN BODY REMOVED BY TRACHEOSTOMY AND NASAL ENDOSCOPY)

  • 임상철;조재식
    • 대한기관식도과학회지
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    • 제2권2호
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    • pp.244-247
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    • 1996
  • Most of bronchial foreign bodies can be removed by ventilation bronchoscopy through transoral route but sometimes, ventilation bronchoscopy through tracheostomy is helpful procedure. Recently, we have experienced a case of bronchial foreign body which could be easily removed by nasal endoscopy and Blakesley forcep instead of bronchoscopy. So we report this case with a review of literatures.

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흉벽에 발생한 Sparganosis;1례 보고 (A Case of Sparganosis in the Chest Wall)

  • 김상익
    • Journal of Chest Surgery
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    • 제25권11호
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    • pp.1240-1244
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    • 1992
  • Human sparganosis caused by Sparganum mansoni, the larval plerocercoid worm of the genus Spirometra, is not uncommon in Korea and is mostly found in subcutaneous or adipose tissue of the abdominal, thoracic wall and inguinal region, but is rarely found in the orbital cavity, brain and breast. It, at present, is a surgical disease because its diagnosis depends almost on the demonstration of the larva[e] from lesion or finding the worm section in surgical pathology specimens. We experienced a case of human sparganosis from a 48 years old woman who had a history of eating a raw frog. We report the case and review the related literatures.

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흉곽출구(경륵) 증후군 수술치험 1례 (Surgical Treatment of Thoracic Outlet Syndrome -A Case Report-)

  • 김홍규;오봉석;이동준
    • Journal of Chest Surgery
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    • 제28권2호
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    • pp.206-208
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    • 1995
  • Thoracic outlet syndrome presents with symptoms resulting from pressure on either the subclavian vessels or the lower trunk of the brachial plexus. It may be caused by a number of abnormalities, including degenerative or bony disorders, trauma to the cervical spine, fibromuscular bands, vascular abnormalities, and spasm of the anterior scalene muscle. We experienced a case of thoracic outlet syndrome [ caused by cervical rib .We report a case with review of literatures.

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유리 족배부 피판을 이용한 경부 식도 재건술;1례 보고 (Cervical Esophageal Reconstruction using Free Fasciocutaneous Dorsal Pedis Flap - One case report -)

  • 조건현
    • Journal of Chest Surgery
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    • 제25권11호
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    • pp.1225-1230
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    • 1992
  • Reconstructive surgical procedures for hypopharyngeal and cervical esophageal defects have still a lot of technical defficulties and varieties to be performed as a optimal treatment according to the clinical situation patient faced. We have experienced a case of successful reconstruction of cervical esophageal defect, which was resulted from graft failure of free jejunal transfer in 43 year old male with eso-phagocutaneous fistula, using free fasciocutaneous dorsalis pedis flap. This article describes the review of our case and literature relevant the reconstructive maneuvers of cervical esophageal defects.

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심장내 발생한 원발성 지방종 1례 보고 (Primary Lipoma of the Heart -A Case Report-)

  • 정일영
    • Journal of Chest Surgery
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    • 제27권4호
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    • pp.310-312
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    • 1994
  • Primary cardiac lipoma is an extremely rare condition. We reports a case of primary lipoma located mainly in the right atrium of the heart in a 58-year-old male patient. The initial presenting symptoms were dyspnea followed by rapidly progress!ve congestive heart failure. Echocardiogram revealed huge mass on right atrium with stalk arising from septum. Under cardiopulmonary bypass the mass was removed and revealed characteristic findings of lipoma on microscope. The patient was recovered without any problem. We would like to describe this case of rare tumor with the review of literatures.

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가육종성 식도암;1례 보고 (Pseudosarcoma of the Esophagus - One Case Report -)

  • 김창회
    • Journal of Chest Surgery
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    • 제24권12호
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    • pp.1197-1200
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    • 1991
  • Polypoid lesions of the esophagus occur infrequently and may be benign or malignant. Pseudosarcoma, a malignant polypoid tumor of the esophagus is rare and appears to be a distinct pathological entity; the polypoid portion is composed of sarcomatous spindle cells and the base of the polyp shows in situ or invasive squamous cell carcinoma. We experienced a case of pseudosarcoma of the esophagus and report the case with the review of literature.

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