• Title/Summary/Keyword: case report

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Bechet`s Disease with Multiple Aterial Abeurysm; A Case Report (Bechet`s disease에 동반된 다발성 동맥류;1례 보고)

  • 조재호
    • Journal of Chest Surgery
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    • v.26 no.4
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    • pp.316-319
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    • 1993
  • Although Behcet`s disease, characterized by oro-genital ulceration and ocular abnormalities, is rare and unfamiliar disease to thoracic surgeon, one must remember that it can cause serious complications on the vascular system such as thrombophlebitis,thrombotic obstuction and aneurysm.We report a case of multiple arterial aneurysms with Behcet`s disease. This 31 year-old female had five times surgical interventions during short period[19 months]. 6 aneurysms were developed in this case, 3 were spontaneous aneurysms, 2 were anastomotic aneurysms and 1 was false aneurysm due to arterial puncture.

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Autotransplantation of tooth into the oroantral fistula site after extraction (상악동 점막 천공부위로의 치아이식)

  • Kim, Yeong-Un
    • The Journal of the Korean dental association
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    • v.41 no.7 s.410
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    • pp.504-508
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    • 2003
  • This report demonstrates a case of tooth autotransplantation into the oroantral fistula site after extraction. Oroantral fistula can be developed when maxillary molar or premolar is extracted in case the root of tooth closed to or inside maxillary sinus. In most of cases, this would heal spontaneously without any interventions. Sometimes, many procedures including flap closure would be used judging from perforating size and previous inflammation. Although fistula size of this case is not that large, closure with tooth autotransplanted has successfully accomplished. So this report will discuss about several clinical aspects.

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Cavernous Hemangioma of the Cauda Equina - A Case Report - (마미총에 발생한 해면상 혈관종 - 증례보고 -)

  • Kim, Keun Su;Ahn, Byeong Jo;Han, Dong Han
    • Journal of Korean Neurosurgical Society
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    • v.30 no.5
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    • pp.662-665
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    • 2001
  • Spinal cavernous hemangiomas of the cauda equina are extremely rare vascular malformations. We report a case of intradural extramedullary cavernous hemangioma of the cauda equina with it's clinical, radiologic and surgical findings. This is the twelveth case of cavernous hemangioma of the cauda equina in the literature. The pertinent literatures are reviewed.

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A Case of Gliosarcoma - Case Report - (뇌 교육종 - 증례보고 -)

  • Ahn, Jung Yong;Kyo, Seo Eui;Joo, Jin Yang
    • Journal of Korean Neurosurgical Society
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    • v.29 no.7
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    • pp.959-962
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    • 2000
  • Gliosarcoma is a rare malignant tumor of the central nervous system consist of gliomatous and sarcomatous elements. The authors report a case of gliosarcoma in the right frontal lobe. Sharp demarcation of the tumor from surrounding tissue and its superficial location may lead to complete removal and prolonged survival despite high malignancy.

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

  • 성시찬
    • Journal of Chest Surgery
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    • v.12 no.4
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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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Bronchogenic cyst communicating with esophagus: report of a case (식도와 연결된 선천성 기관지성 낭종의 치험 1례 보)

  • Lee, Cheol-Ju;Choe, Won-Hui;Ha, Jeong-Ok
    • Journal of Chest Surgery
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    • v.17 no.3
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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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Pulmonary Blastoma -A Case Report- (폐아세포종 -수술치험 1례-)

  • 금동윤
    • Journal of Chest Surgery
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    • v.27 no.10
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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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Surgical Treatment of Thoracic Outlet Syndrome -A Case Report- (흉곽출구(경륵) 증후군 수술치험 1례)

  • Kim, Hong-Gyu;O, Bong-Seok;Lee, Dong-Jun
    • Journal of Chest Surgery
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    • v.28 no.2
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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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Intra-Root Cavernous Angioma of the Cauda Equina : A Case Report and Review of the Literature

  • Chun, Sang-Woo;Kim, Sang-Jin;Lee, Tae-Hoon;Koo, Hye-Soo
    • Journal of Korean Neurosurgical Society
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    • v.47 no.4
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    • pp.291-294
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    • 2010
  • Authors experienced intra-root cavernous angioma which is very rare case among cavernous angiomas of cauda equina. Our intra-root cavernous angioma was confirmed by findings from operating field and microscopic examination. We report this case with review of the literature.