• Pediatric Infection and Vaccine
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• 제14권1호
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• pp.75-82
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• 2007

목 적 : hMPV는 paramyxovirus에 속하는 RNA 바이러스로 2001년 van den Hoogen 등에 의해 처음으로 보고되었으며 늦은 겨울이나 이른 봄에 영아와 노인에서 호흡기 감염을 일으키는 바이러스로 알려져 있으나 아직 우리나라에서의 보고는 많지 않다. 최근 호흡기 증상을 보이는 환아들에서 hMPV를 확인한 바 있어 이에 보고하는 바이다. 방 법 : 2004년 10월부터 2005년 5월까지 을지병원, 서울의료원, 보라매병원 소아과에 호흡기 증상을 주소로 방문한 443명의 비인두 흡인물에서 hMPV RT-PCR을 시행하였고, 양성인 15명의 임상 양상과 검사 소견을 의무기록을 통해 후향적으로 조사하였다. 결 과 : 443명 중 15명에서 hMPV PCR 양성을 보여 양성율은 3.4%이었다. 남아가 7명, 여아가 8명이었고 연령은 1개월에서 62개월(정중값 31.5개월)이었다. 이중 24개월 미만의 환아가 53.3%(8/15)이었다. 진단명은 폐렴 9명, 모세기관지염 3명, 상기도염 2명, 후두염 1명이었다. 그 중 1명에서 천식이 있었고 나머지 환아에서는 기왕력이 없었다. 임상 증상으로는 기침이 15명(100%)으로 가장 많았고 그 외 열감 12명(80%), 콧물 10명(67%), 구토 4명(27%), 호흡 곤란 4명(27%), 설사 3명(20%), 발진 1명(7%)이 있었다. 신체 검진 상 인두 발적이 가장 흔하게 보이는 소견이었으며 나음 6례, 흉부 함몰 4례, 빈호흡 2례, 천명 2례, 천음 1례가 관찰되었다. 말초 혈액 검사만으로 hMPV 감염을 시사하는 특징적인 소견은 없었다. 15명 중 2명에서 아데노바이러스와 중복감염이 있었다. 평균 발열 기간은 $4.9{\pm}2.8$일이었으며 입원 치료를 하였던 13명의 평균 재원 기간은 $5.6{\pm}0.9$일이었고 모두 대증적 치료 후 합병증 없이 증상 호전을 보여 퇴원하였다. 결 론 : hMPV는 상기도 및 하기도 호흡기 감염의 중요 원인 바이러스 중 하나로 생각되며 우리나라에서의 임상적, 역학적 특징을 규명하기 위해서는 향후 더 많은 환자를 대상으로 한 연구가 필요할 것으로 사료된다.

• Journal of Chest Surgery
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• 제36권11호
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• pp.839-845
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• 2003

배경: 결핵에 대한 화학요법이 확립되고 유병률의 점진적인 감소를 보이고 있는 현재에도 다제내성 폐결핵은 여전히 불량한 치료성적과 장기생존율의 저하를 초래하고 있다. 이 연구는 다제내성 폐결핵의 수술예를 분석하여 이 질환에 대한 폐절제술의 유용성과 위험정도를 알아보고자 하였다. 대상 및 방법: 1990년 2월부터 2002년 2월까지 다제내성 폐결핵으로 폐절제술을 시행한 20명, 21예를 대상으로 후향적 조사를 하였다. 남자는 14예, 여자는 6예였으며 평균연령은 42.8$\pm$12.1세였다. 환자들이 최초 폐결핵을 진단 받고 수술까지 평균 10.3$\pm$7.6년이 경과되었다. 술 전 객담도말검사에서 13예 (65%)가 양성이었으며, 내성 검사상 모두 INH와 RFP을 포함한 평균 3.5개의 항결핵제에 내성을 보였다. 술 전 방사선학적 검사상 15예(75%)에서 공동성 병변을 관찰할 수 있었고, 양측 폐야를 침범한 경우가 3예 있었으나 주 병변은 모두 편측에 존재했다. 13예(75%)의 경우 내과적 치료로 균음전에 실패하였고 2예(10%)는 지속적인 객혈로, 5예(25%)는 높은 재발의 가능성을 가진 결핵성 병변을 원인으로 수술을 하였다. 수술은 전폐적출술 9예(40%), 폐엽전제술 9예(45%), 폐엽절제술 및 구역절제술 3예(15%)였다. 환자들의 술 후 평균 추적기간은 23개월이었다. 결과: 수술 사망은 없었으며 술 후 합병증은 총 11예로 장기간의 공기 누출 3예, 재수술을 요하는 출혈 3예, 기관지늑막루로 인한 농흉 2예였고 무기폐, 창상감염 및 흉벽루가 각각 1예였다. 수술 직후 11예(85%)에서 균음전이 이루어졌고 2예가 균음전에 실패하였다. 술 후 균음전환자 1예에서 수술 11개월째에 재발하였으나 추가로 전폐 절제술을 시행하여 완치하였다. 결론: 환자의 폐기능이 충분하며 적절한 절제가 가능한 병변일 경우 다제내성 폐결핵은 수술요법과 약물요법의 병합으로 높은 비율의 균음전과 완치를 이룰 수 있으며 심각한 합병증 또한 많지 않음을 확인할 수 있었다.

• Journal of Chest Surgery
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• 제8권2호
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• pp.109-118
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• 1975

This is a report on four cases of the lobar emphysema due to proximal bronchial obstruction in the Department of Thoracic Surgery, Hanyang University Hospital, during the period of three and half years from 1972 to 1975. First case, a two years old male child was referred to our Department with the lobar emphysema of the lower lobe of the right lung with pneumonia. This emphysema was developed after aspiration of a piece of peanut. Bronchoscopy revealed that the bronchus of the right lower lobe was obstructed with the foreign body, however removal of the peanut through bronchoscope was not attempted because of corruption and softening of the peanut. The removal of the peanut by bronchotomy was performed after subsiding of acute phase of pulmonary infection. Postoperative course was uneventful and the emphysema was disappeared. Second case, a twenty months old female baby was referred to our Department with lobar emphysema of the lower lobe of the left lung. The emphysema was suddenly developed with coughing and dyspneic symptoms and the diagnosis was made roentgenologically. She gave a history of reccurrent infections of the respiratory tract after birth. Bronchoscopy showed an obstruction of the left main bronchus with the growing of fibrinous tissue on the bronchial mucosa. The protruded tissue in the left main bronchus taken out about O.8ml with biopsy forceps for histological examination. After this procedure, the emphysema of the left lung was disappeared. Histological finding was reported to be a chronic inflammatory granulation tissue. Third case, a two and half years old male child was referred to our Department with roentgenological lobar emphysema. Two weeks prior to admission he had an episode of sudden onset of coughing attack with dyspnea. Bronchoscopy revealed that the bronchus of the left lower lobe was obstructed with a mass which was strongly suspected of a neoplastic tissue. At operation, there was found a perforation of enlarged tuberculous lymph node in the bronchus of the left lower lobe and protrusion of granulation tissue into the bronchus. Ruptured orifice on themembranous wall of the left lower lobe bronchus was closed with interrupted suture after the" removal of a perforated tuberculous lymph node. Postoperative course was uneventful and antituberculous chemotherapy was given. Fourth case, a 47 years old man was admitted to our Department with the complaint of severe dyspnea of few months duration. Twenty years ago, he had a history of lung tuberculosis and was treated for many years. X-ray examination including tomography and bronchography revealed that the upper lobe of the right lung was destroyed with cavities, the lower lobe was completely shrunk, and the right middle lobe was strongly overdistended with narrowing bronchial trees. Differential bronchospirometry and lung scanning confirmed that the respiratory function of the affected lung was impaired almost totally. The value of the right lung was calculated on 6% of oxygen uptake, 1% of Minute volume, and 32% of vital capacity. The right pneumonectomy was performed under the careful consideration of anesthetic and surgical procedures. Postoperative course was uneventful and the respiratory function was improved nearly to the normal level.evel.

• Journal of Chest Surgery
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• 제12권3호
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• pp.281-288
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제12권3호
• /
• pp.289-296
• /
• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• 한국산학기술학회논문지
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• 제16권8호
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• pp.5508-5512
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• 2015

서론: 인체 스파르가눔은 드물며, 기생부위는 일정치 않으나 주로 흉벽, 복벽, 대퇴 및 음낭 등의 피하조직 및 근육 사이 근막이며 그 외 안와, 흉강, 복강, 척수강 및 중추신경계에서 발생하기도 한다. 이중 유방 스파르가눔증은 드물다. 대상 및 방법: 저자는 76세의 여자 환자에서 감염된 물을 통해 생긴 3년 이상 유방에 움직이며 머무른 것으로 보이는 두 곳의 유방 스파르가눔증을 경험하였다. 환자는 뱀, 개구리 등을 생식하는 과거력은 없었으나 평소 약수를 즐겨마셨다. 유방암으로 오인하여, 이 유방 스파르가눔증에 대해 유방촬영술, 유방초음파, MRI, PDG PET/CT 등을 시행하였고, 외과적 절제술 시행하여 치료하였다. 결론: 인체 감염 경로는 크게 3 가지로, 첫째, 오염된 물을 섭취하는 경우, 둘째, 뱀, 개구리 등을 생식하는 경우, 셋째, 환부에 감염된 뱀, 개구리 근육을 부착하는 경우로, 이중 물에 의한 감염 보고는 국내에 거의 없다. 유방 스파르가눔증에 대해 유방초음파, MRI가 도움이 되는 것으로 알려져 있으나, 하나의 병변에 대해 유방촬영술, 유방초음파, MRI, FDG PET/CT 모두를 보고한 것은 현재 없다. 이에 병리 검사 결과, 영상결과와 더불어 관련된 문헌 고찰과 함께 알아보고자 한다.

• Archives of Plastic Surgery
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• 제38권5호
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• pp.559-566
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• 2011

Purpose: The use of tissue expander/implant in breast reconstruction using tissue expander-implant is one of the most common surgical procedures. The use of AlloDerm as a sling to reestablish the lower pole of the pectoralis major muscle results a decrease in morbidity compared with more invasive procedures. However the use of AlloDerm is more expensive than other options. We decided to compare AlloDerm with Permacol, which has been safely used in human body reconstruction and is less costly than AlloDerm. Methods: After mastectomy, the inferolateral origin of the pectoralis major muscle was elevated. Either AlloDerm or Permacol was sutured to the chest wall at the level of the previously marked inframammary fold. The lower border of the pectoralis major muscle and the upper portion of the crescent-shaped piece of either AlloDerm or Permacol was sutured together using a tension free technique, and a tissue expander was subsequently inserted into the subpectoral-subAlloDerm (or Permacol) dual pocket. Results: AlloDerm was used in twenty-one patients (28 breasts) and Permacol was used in six patients (11 breasts) for tissue expander-implant breast reconstruction. During the mean follow-up period of 17 months (8~25 months). Two infections (7%) occurred in AlloDerm cases and four infections (36%) occurred in Permacol cases. Conclusion: This study is the first comparison of tissue expander/implant breast reconstruction using AlloDerm and Permacol. The use of Permacol resulted in more postoperative infection compared with the use of AlloDerm. This report is still limited with the small number of cases studied.

• Tuberculosis and Respiratory Diseases
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• 제45권5호
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• pp.1058-1066
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• 1998

연구배경: 흉부 방선균 감염에서 흉곽벽 혹은 늑골까지 폐 방선균 감염이 파급되는 경우는 감소되고 있는 것으로 보고 되었다. 또한 흉부 방선균증은 흔한 질환이 아니고 아급성 내지는 만성 폐 감염의 경과를 보이프로 폐결핵 혹은 폐암과의 감별 진단이 어려운 것으로 알려져 있다. 아직 진단 방법에 대해 추천되는 것은 없는 실정이며 기관지경 검사의 역할에 대해서는 아직 자세히 기술된 적은 없었다. 저자들은 총 17예의 흉부 방선균증을 경험하였고 진단에 있어서 기관지내시경의 역할과 타호흡기 질환과의 동반 여부에 대하여 보고하는 바이다. 연구방법: 1989년 이래 서울중앙병원에 입원하여 흉부 방선균증으로 진단되었던 17예(연령 24~72세, 평균 53세 ; 남녀 비 11 : 6)의 임상적 특징을 후향적으로 분석하였다. 연구결과: 흉부 방선균종의 진단시 증상은 기침이 14예(82%)로 가장 많았고, 객혈 8예, 화농성 객담 8예, 흉막염성 흉통 6예 순이었으며, 체중 감소와 만성 피로감이 각 6예에서 관찰되었고, 섭씨 38.3도 이상의 발열이 있었던 예는 없었다. 증상 발현에서 진단까지의 기간은 평균 6개월 (3주~2년)로서 폐결핵의 추정 진단하에 항결핵제를 5예에서 투여하였다. 기저 폐질환으로는 기관지 확장증이 2예, 폐기종이 1예였고, 과거 폐결핵 병력이 있었던 예는 5예로서 이 중 2예에서 다시 항결핵제 투여를 하고 있었다. 흉부 방사선 촬영 소견은 폐종괴 8예, 무기폐 3예 및 폐렴 소견 3예로서 상기 소견은 모두 1개 폐엽에 국한되었고 이중 흉막염 동반에는 1예였으며, 나머지 3예는 정상 소견이었다. 확진전 임상적 추정 진단은 폐암에 11예, 그리고 폐결핵이 6예였다. 흉부 방선균중이 진단된 방법은 기관지 내시경하 조직 검사에 의해 7예, 세척세포진이 2예였고, 경피적 세침 흡인술 3예, 폐엽 절제술 및 종격동경 검사가 각각 4예 및 l예였다. 기관지 내시경 검사 육안 소견은 점막 종창에 의한 기관지 협착이 5예, 종괴 5예, 그리고 기판지가 괴사 물질로 덮인 경우가 3예에서 관찰되었으며, 정상 소견은 3예였다. 최종 진단은 방선균 폐렴 10예, 기관지 방선균증 6예, 그리고 종격동 임파선 방선균 감염 1예 였으며, 폐외 병소 감염이 있었던 예는 1예로서 다발성 뇌결절의 양상을 보였다. 객담 결핵균 검사상 도말은 음성이었으나 배양이 양생인 예가 2예 있었고, 폐암과의 공존 예도 2예 있었다. 항생제 치료를 시행한 16예 중에서 1예는 폐암으로 사망하였고, 지속적 치료가 가능하였던 15예에서 항생제 치료 기간은 평균 9.2개월이었고, 경구 약제 복용을 중단한 1예에서 재발이 있었다. 결 론: 흉부 방선균증은 만성의 비교적 국소성인 폐질환으로 폐암 혹은 폐결핵과 유사한 양상을 보이고, 상기 질환들과의 공존 가능성도 염두에 두어야 한다. 또한 흉부 방선균증은 병변의 위치가 중심부인 경우는 기관지 내시경이 중요하고, 말초부인 경우는 경피적 세침 흡인술이 중요할 것으로 사료된다.