식도천공의 임상적 평가

전순호,정태열,송동섭,김혁,함시영,이철범,강정호,정원상,김영학,지행옥,Chon, Soon-Ho,Chung, Tae-Yul,Song, Dong-Sub,Kim, Hyuck,Hahm, Shee-Young,Lee, Chul-Burm,Kang, Jung-Ho,Chung, Won-Sang,Kim, Yong-Hak,Jee, Heng-Ok 대한흉부심장혈관외과학회 2000 Journal of Chest Surgery (J Chest Surg) Vol.33 No.1

Background: Esophageal perforation is an extremely lethal injury that requires careful management for survival,. Material and Method: We performed a retrospective clinical revi-ew of 14 patients treated for esophageal perforation at the Department of Thoracic and Cardiovascular Surgery hanyang University Hospital between July 1986 and August 1998. Cardiovascular Surgery Hanyang University Hospital between July 1986 and August 1998. Result: The ration between male and female patients was 12:2 and their ages ranged from 9 to 68 years( average: 446 years). Iatrogenic perforations were found in 6 patients(42.9%) spontaneous perforations in 3 patients(21.4%) traumatic perforations in 2 patients(14.3%) and caustic perforations foreign body origin and esophagel cancer in 1 patient (7.1%) each. Four of the patients(28.6%) had esophageal ruptures located cancer in 1 patient (7.1%) each. Four of the patients (28.6%) had esophageal ruptures located in the cervical esophagus and 10 patients (71.4%) in the thoracic esophagus, The most frequent location was in the mid third portion of the esophagus (35.7%) there were also 2 patients(14.3%) in the upper third portion and 3 patients(21.4%) in the lower third portion. Complications encountered included mediastinitis empyema or pleural effusion mediastinal or lung abscess sepsis and aspiration pneumonia. The most frequent complication that occurred was mediastinitis in 9 cases (57%) Three patients underwent conservative treatment. Among the patients who underwent surgical treatment 5 patients underwent primary closure 6 patients underwent open drainage and 2 patients underwent reconstrumction (1 patients had an initial primary closure and 1 patient had an initial open drainage procedure). The mortality rates for those with conservative and surgical treatment were 66.7% (2cases) and 9.1% (1 cases) respec- tively. Conclusion: Perforation of the esophagus although very rare has a high mortality rate and thus aggressive operative therapy is necessary.

중 전상부 종격동의 중피낭종 -수술 치험 1례-

전순호,강정호,지행옥,김영학,정원상,김혁,박문향,서정국,진석철,Chon, Soon-Ho,Kang, Jung-Ho,Jee, Heng-Ok,Kim, Young-Hak,Chung, Won-Sang,Kim, Hyuk,Park, Moon-Hyang,Suh, Jung-Kook,Jeon, Seok-Chul 대한흉부심장혈관외과학회 1998 Journal of Chest Surgery (J Chest Surg) Vol.31 No.10

중피낭종은 심막체벽낭종, 스프링워터낭종, 장막낭종 등 여러 가지 이름으로 명명되고 있다. 대부분의 중피낭종은 심낭의 기형으로 부터 발생 된다고 하나, 본 증례는 늑막기형에서 발생된 아주 희귀한 중피낭종이므로 조직학적으로 특수 염색을 통하여 확진하게 되었다. 본 증례는 64세 여자 환자로서 입원 당시 우측 목 부위에 통증 없는 낭성 종괴가 만져져 외래를 통하여 내원케 되었다. 컴퓨터 단층촬영상 종격동 림프관종이라는 진단하에 수술을 시행하여 낭성종괴를 완전 절 제 하였다. 수술후 절제된 조직소견 결과 종격동 중피낭종이 확진 되었으며 수술후 환자는 큰 후유증 없이 완치되어 퇴원 하였다. Mesothelial cysts have many other names, such as pericardial celomic cyst, pleura- diaphragmatic cyst, simple cyst of the mediastinum, springwater cyst, serosal cyst, etc. (Petereit 1972, Drash 1950). Most mesothelial cysts are believed to originate from malformations of the pericardium, but some, like the one in this case, are believed to result from a pleural malformation. (Ochsner 1966, Lambert 1940). Mesothelial cysts are extremely rare and can be confirmed histologically by special stains. A 64 year old woman was admitted due to a painless bulging mass in her right neck. The operation was performed with the initial diagnosis of cystic lymphangioma confirmed by computer tomography and total excision was possible. The diagnosis of mesothelial cyst of the mediastinum was confirmed by histologic examinations (stainings) and the patient was discharged from the hospital without any significant complications.

CS 가스 흡입이 흰쥐의 폐포막내 Laminin-1에 미치는 영향

전순호 ( Soon Ho Chon ),백두진 ( Doo Jin Paik ),이철범 ( Chul Burm Lee ),김혁 ( Hyuck Kim ),정원상 ( Won Sang Chung ),김영학 ( Young Hak Kim ),강정호 ( Jung Ho Kang ),지행옥 ( Heng Ok Jee ) 대한결핵 및 호흡기학회 2005 Tuberculosis and Respiratory Diseases Vol.59 No.4

둔기손상에 대한 쇄골골절에 생긴 외상성 쇄골하동맥 박리: 폐쇄가 길면 수술하느냐 또는 스텐트를 삽입하느냐?

전순호 ( Soon Ho Chon ),이길수 ( Kil Soo Yie ),강재걸 ( Jae Gul Kang ) 대한외상학회 2015 大韓外傷學會誌 Vol.28 No.3

Subclavian injuries in blunt trauma are reported in less than 1% of all arterial injuries or chest related injuries. We report a female 68 yr-old patient whom has visited our emergency center due to a motorcycle traffic accident with complaints of right chest wall and shoulder pain. Her injury severity score was 22 and she was found with a comminuted clavicle fracture and subclavian artery injury. She developed delayed symptoms of pallor, pain and motor weakness with loss of pulse in her right arm. Attempts at intervention failed and thus, she underwent emergency artificial graft bypass from her subclavian artery to her brachial artery. Her postoperative course was uneventful and she is happy with the results. Although rare, a high index of suspicion for the injury must be noted and the inevitable surgical option must always be considered. [ J Trauma Inj 2015; 28: 219-221 ]

악성간엽종의 외과적 치료 -1례보고-

양수호,전양빈,전순호,김혁,정원상,최요원,전석철,전석훈,박문향,지행옥,Yang, Soo-Ho,Chon, Yang-Bin,Chon, Soon-Ho,Kim, Hyuk,Chung, Won-Sang,Choi, Yo-Won,Chon, Suk-Chul,Chon, Suk-Hoon,Park, Moon-Hyang,Jee, Heng-Ok 대한흉부심장혈관외과학회 1998 Journal of Chest Surgery (J Chest Surg) Vol.31 No.2

악성 간엽종은 유아와 태생기에서 매우 드문 종양이다. 악성간엽종은 성인에서 극히 드물고 섬유조직이외의 둘 또는 그 이상의 간엽성분으로 구성된 종양으로 결체조직의 어떤 형태로도 분화할 가능성이 있는 태생기 간엽에서 기원한다고 생각된다. 환자는 61세 남자로 2개월 전 가래를 동반한 기침을 주소로 검사를 받던 중 우폐상부에 매우 큰 종괴를 보이는 암종으로 입원하였다. 환자는 우폐상부 미세침윤조직검사상 편평상피세포암 의심하에 우전폐절제술을 받았다. 수술장 소견상 종괴는 흉벽과 심하게 유착되었으며 우폐하부까지 침습된 소견을 보이는 악성간엽종으로 진단되었다. 환자는 수술후 5,000rad의 방사선 조사를 받고 수술후 6개월째인 현재까지 재발징후없이 경과 관찰중이다. Malignant mesenchymoma is a very rare tumor presented during the embryonic and infant period and malignant mesenchymoma in the adult is extremely rare. Tumor is composed of two or more unrelated mesenchymal derivatives apart from fibrous tissue. These tumors are thought to be originated from embryonic mesenchyme capable of differentiating into any type of connective tissue. A 61 years old man with complaints of cough and copious sputum of onset of two months was admitted after initial examinations, showing a very huge mass over the right upper lobe. Right pneumonectomy with partial rib resection of 3rd, 4th, and 5th ribs was performed due to the initial diagnostic impression of squamous cell carcinoma by the fine needle aspiration biopsy. The operative field presented a mass locating across the interlobal fissure with severe adhesions to the chest wall. Postoperatively, the patient received 5,000 rads of radiotherapy and presently, 6 months later, has shown no signs of recurrence.

원발성 흉벽종양의 임상적 고찰

손상태,전순호,신성호,김혁,정원상,김영학,강정호,박문향,지행옥,Sohn, Sang-Tae,Chon, Soon-Ho,Shin, Sung-Ho,Kim, Hyuck,Chung, Won-Sang,Kim, Young-Hak,Kang, Chung-Ho,Park, Moon-Hang,Jee, Heng-Ok 대한흉부심장혈관외과학회 1998 Journal of Chest Surgery (J Chest Surg) Vol.31 No.10

연구배경 : 흉벽종양은 연부조직 종양과 골조직 종양으로 대별할 수 있으며 이를 다시 양성종양과 악성종양으로 구분할 수 있다. 재료 및 방법 : 한양대학병원 흉부외과 교실에서는 1973년 1월 부터 1997년 9월까지 치료한 원발성 흉벽종양 68례를 경험한 바, 이에 보고하는 바이다. 결과 : 환자는 총 68명으로 이중 남자가 33명 (48.5%), 여자가 35명(51.5%) 이었다. 환자의 연령은 10세에서 79세 사이로 평균연령은 39.4세이었다. 환자의 연령별 분포는 30대가 23명 (33.8%), 50대가 12명 (17.6%), 40대가 10명 (14.7%) 순이었다. 전체 종양중 양성종양이 53례이었고, 악성종양이 15례이었다. 양성종양은 30대에서 17례(32.1%), 악성종양은 30대에서 6례 (40%)로 나타나, 악성종양과 양성종양 모두 30대에서 가장 많았다. 양성종양중 섬유성 이형성증과 연골종이 각각 14례 (26.4%) 씩으로 가장 많았고, 골연골종과 지방종이 각각 8례 (15.1%) 씩이었다. 악성종양은 골육종이 8례(53.3%)로 가장 많았다. 종양의 발생부위는 골 및 연골조직이 49례, 연부조직이 19례이었다. 환자의 증상은 전례에서 종괴가 만져졌고 압통을 호소한 환자가 51례, 흉벽종양이 폐를 침범한 3례에서 호흡곤란을 호소하였다. 악성종양중 6례 (40%)에서 광범위 절제술을 하였고, 양성종양은 4례 (7.7%)에서 광범위 절제술을 하였다. 수술 후 인대양 종양 1례에서 재발을 하였다. 수술이나 수술 후 합병증으로 인한 사망자는 없었다. 결론 : 원발성 흉벽종양은 환자의 대부분에서 종괴가 만져져 내원하는 경우가 많았으며, 양성종양인 경우 절개로 치유되지만 악성종양인 경우 흉벽의 광범위 절개가 요구되고 이에 따른 흉벽 재건술이 필요할 수 있다. Background: Chest wall tumors can classified into soft tissue tumors and bone tissue tumors and can be subclassified into benign and malignant tumors. Materials and methods: We report an analysis of 68 patients with primary chest wall tumors treated at the department of thoracic and cardiovascular surgery at Hanyang University Hospital from January, 1973 to September 1997. Results: Among a total of 68 patients 33(48.5%) were males and 35(51.5%) were females. The ages of the patients ranged from 10 to 79 years with a mean age of 39.3 years. According to the age distribution, 23 patients (33.8%) were from the 4th decade, 12 patients(17.6%) were from the 6th decade, and 10 patients(14.7%) were from the 5th decade. Among the primary chest wall tumors, 53 cases were benign and 15 cases were malignant. Among the benign tumors, 17 cases(32.1%) were in the 4th decade and among the malignant tumors, 6 cases(40%) were in the 4th decade. In both malignant and benign tumors the most common ages were in the 4th decade. The most common tumors were fibrous dysplasia and chondroma, each with a total of 14 cases(26.4%). Osteochondroma and lipoma each had 8 cases(15.1%). Among malignant tumors, osteosarcoma was most common with 8 cases (53.3%). According to location, 49 cases occured in both bone and cartilage tissue, 19 cases occurred in cartilage. Among the presenting symptoms, palpable mass was present in all cases. Fifty-one patients complained of tenderness and among cases with involvement of the lung, 3 patients had complained of respiratory distress. Among the malignant tumors 6 cases underwent a radical operation and 4 cases of benign tumors underwent a radical operation. Postoperativly, there was one case with recurrence from a desmoid tumor. There were no deaths postoperativly and no deaths due to complications(and their postoperative courses were uneventful). Conclusions: Most patients with primary chest wall tumors initially present with mass at admission. Resection is sufficient treatment for benign tumors but in malignant tumors wide resection of the chest wall is needed and mchest wall reconstruction.

폴란드 증후군 -1례 보고-

신성호,전양빈,전순호,강정호,김혁,정원상,김영학,지행옥,Shin, Sung-Ho,Chon, Yang-Bin,Chon, Soon-Ho,Kang, Jung-Ho,Kim, Hyuk,Chung, Won-Sang,Kim, Young-Hak,Jee, Heng-Ok 대한흉부심장혈관외과학회 1998 Journal of Chest Surgery (J Chest Surg) Vol.31 No.9

Poland씨 증후군과 관련된 흉벽기형은 매우 드문 질환으로 선천적으로 대흉근의 흉골부 결손과 한쪽 상지의 다양한 기형을 동반한다. 또한 Poland씨 증후군의 다른 임상적 특징은 유방과 유두의 결손 및 저형성, 피하 지방과 액모의 결손, 늑연골 및 늑골전면부의 이상을 포함한다. 그 기원은 확실하지 않으나 유전과는 관계 가 없는 것으로 알려져 있다. Poland씨 증후군은 심한 정신적인 그리고 신체적인 문제를 일으킬 수 있으며 초기 발견 및 수술적 교정이 이득이 될 것으로 생각된다. 본원은 Poland씨 증후군으로 진단된 37세 남자환자를 성공적으로 수술치험하였기에 이를 보고하는 바이다. The chest wall deformity associated with Poland's syndrome is a very rare anomaly which consists of congenital unilateral absence of the sternal head of the pectoralis major muscle and various abnormalities of the upper extremity. Other clinical features associated with Poland's syndrome include deficiency or absence of the breast and nipple, deficiency of subcutaneous fat and axillary hair, and abnormalities of costal cartilages and anterior ends of ribs. The origin remains uncertain, but is considered not to be hereditary. Poland's syndrome may pose a serious psychologic and cosmetic problem, early recognition and surgical correction may prove beneficial. A 37 year old patient with Poland's syndrome was encountered and underwent satisfactory surgical correction.

증례 : 신장 ; 혈액투석 환자의 심낭삼출의 치료에 시도한 흉강경을 이용한 심낭막 개창술

류지원 ( Ji Won Ryu ),이주현 ( Ju Hyun Lee ),홍현석 ( Hyun Suk Hong ),이주학 ( Joo Hark Yi ),전순호 ( Soon Ho Chon ),한상웅 ( Sang Woong Han ),김호중 ( Ho Jung Kim ) 대한내과학회 2010 대한내과학회지 Vol.78 No.2

저자들은 투석에 반응하지 않는 요독성 심낭삼출에 대해서 진단 및 치료 목적으로 직경 2~3 mm 미세흉강경을 이용해 심낭흉막개창술을 시술한 후 42개월 추적관찰 동안 심낭삼출의 재발 및 시술에 따른 합병증 없이 없었고, 외관상 흉터가 거의 남지 않는 장점을 경험하여 보고하는 바이다. With the advent of 2-and 3-mm endoscopic instruments, a thoracoscopic pericardiectomy can be performed with relative ease and with almost no postoperative scar. We report a case of a 40-year-old woman with end-stage renal disease who had a large volume of

위팔동정맥루 구제를 위한 노쪽피부정맥의 지연 표재전위 : A Case Report

이홍기,박훤겸,남영수,백홍규,전순호 대한혈관외과학회 2004 Vascular Specialist International Vol.20 No.1