배 경 : 중환자에서 질환의 중증도 평가체계는 예후를 평가하는데 유용한 것으로 알려져 있다. 하지만 이들은 다소 복잡하고 비용-효과 면이 있어 보다 손쉽게 예후를 예측할 수 있는 troponin-I, lactate, CRP 등과 같은 생화적 지표에 대한 연구가 진행되어 왔다. 본 연구는 비 순환기계 중환자에서 troponin-I, lactate, CRP 수치가 예후 인자로서 유용한지를 알아보고자 하였다. 대상 및 방법 : 2003년 9월부터 2004년 6월까지 경상대학교 병원 내과계 중환자실에 비 순환기계 질환으로 입원한 환자 139명(63.3 14.7세, 남:여=88:31)을 대상으로 하였다. 중환자실 입원 24시간내 APACHE Ⅱ, SAPS Ⅱ와 SOFA 점수를 이용해 질환의 중증도와 다장기부전의 정도를 평가하였고 troponin-I, lactate, CRP 수치를 측정하였다. 중환자 입원 후 재원 10일째와 30일째 생존군과 비 생존군의 troponin-I, lactate, CRP 수치를 서로 비교하였고 troponin-I, lactate, CRP 수치가 정상인 군과 비정상인 군간의 재원 10일째 및 30일째 사망률을 비교하였다. 또한 각 지표와 중증도 평가 체계인 SAPS Ⅱ와 SOFA 점수와의 상관 관계를 조사하였다
배 경 : 국내에서 전향적으로 DILD를 등록하여 원인 분류한 보고가 없고 진단 수기 및 치료에 대한 보고도 전무하여, 한 3차 대학병원에서 2년 동안 전향적으로 진단된 DILD의 원인, 진단 수기 및 치료현황에 대한 실태를 파악하고자 본 연구를 시행하였다.방 법 : 2002년 5월부터 2004년 4월까지 2년간 삼성서울병원에서 전향적으로 등록된 DILD 환자 487명을 대상으로, 2002년 ATS/ERS 분류에 따른 원인, 진단에 이용된 수기, 치료 방법에 대해 후향적 조사를 시행하였다.
Introduction : Diffuse interstitial lung diseases (DILD) comprise of a large group of lung diseases with diverse etiologies. They are classified into four categories based on the etiology and pathological findings. In Korea, epidemiological data on DILD has never been reported in a prospective manner. Method : From May 2002 to April 2004, total 487 patients with DILD were prospectively registered at Samsung Medical Center. The prospective observational analysis of the etiologies, its classification based on 2002 ATS/ERS (American Thoracic Society/European Respiratory Society) guidelines, as well as diagnostic tests and the retrospective analysis of the treatment modalities were carried out. Any infectious and malignant causes were excluded. Results : 1) The patients were classified into idiopathic interstitial pneumonia (IIP) in 269 patients (55.2%), known causes of DILD in 168 patients (34.5%), sarcoidosis in 27 patients (5.5%), other forms of DILD in 14 patients (2.9%), and undetermined DILD in 9 patients (1.9%). 2) The diagnostic test showed that most patients had undergone chest high resolution computed tomography (HRCT) and pulmonary function test (PFT) (97%, 89%). Transbronchial lung biopsy (TBLB) and surgical lung biopsy (SLB) were performed in limited patients (38%, 29%). 3) Among 269 patients with IIP, 220 (82%) had idiopathic pulmonary fibrosis (IPF) while 23 (9%) had nonspecific interstitial pneumonia. SLB was carried out in 36% of patients with IIP. 4) Symptomatic supportive care was given to 67% of IPF, but specific medical treatment including corticosteroids was administered to 89% of non-IPF patients. Conclusion : A nationwide registry of DILD patients is required to determine the annual incidence, etiology, and practice pattern of diagnosis and treatment in Korea. (Tuberc Respir Dis 2005; 58: 570-575)
배 경 : 기관지 방선균증은 매우 드문 질환이다. 본 연구는 최근 10년간 조직학적으로 진단된 7명의 기관지 방선균증 환자의 임상상과 치료에 대해 살펴보고자 하였다. 대상 및 방법 :1994년 10월부터 2003년 12월까지 삼성서울병원에 내원하여 기관지 방선균증으로 진단된 7명의 임상적, 방사선학적 특징과 치료에 대해 후향적 분석을 시행하였다.
Background : Thoracic actinomycosis is a relatively uncommon anaerobic infection caused by Actinomyces israelii. There have been only a few case reports of endobronchial actinomycosis. The aim of this study was to evaluate the clinical manifestation and treatment of endobronchial actinomycosis. Material and Methods : Seven patients with endobronchial actinomycosis, who were diagnosed in the past 10 years, were retrospectively reviewed. Results : Cough and sputum were the most common symptoms. The chest radiograph and computed tomography showed necrotic consolidation (n=3), atelectasis (n=2), mass (n=1) and an endobronchial nodule (n=1). Proximal broncholithiasis was observed in five patients. All cases were initially suspected to have either lung cancer or tuberculosis. In these patients, the median duration of intravenous antibiotics was 3 days (range 0-12 days) and the median duration of oral antibiotics was 147 days (range 20-412 days). Two patients received oral antibiotic therapy only. There was no clinical evidence of a recurrence. Conclusion : Endobronchial actinomycosis frequently manifests as a proximal obstructive calcified endobronchial nodule that is associated with distal post-obstructive pneumonia. The possibility of endobronchial actinomycosis is suggested when findings of broncholithiasis are present at chest CT. The traditional recommendation of 2-6 weeks of intravenous antibiotics and 6-12 months of oral antibiotic therapy are not necessarily essential in all cases of endobronchial actinomycosis. (Tuberc Respir Dis 2005; 58: 576-581)
배 경 : 지역사회획득폐렴은 진단 및 치료의 연구 발전에 비해 사망률이 높은 질환이다. 입원환자에서 조기 사망률은 높지만 이와 연관된 인자에 대한 연구는 빈약하다. 이에 저자들은 기존 자료를 바탕으로 응급실에서 지역사회획득폐렴으로 방문하여 조기 사망한 환자들을 분석하여 관련인자를 파악하고자 하였다.방 법 : 1999년 1월부터 2004년 7월까지 지역사회획득폐렴으로 응급실 방문하여 호흡기 내과로 입원한 환자 1487명중에서 방문 후 48시간 내에 사망한 환자 30명과 치유되어 퇴원한 환자 중 나이와 성별을 짝지은 60명을 대조군으로 비교분석하였다.
Background : Early death is an important problem associated with the management of community-acquired pneumonia. However, there is little information on the risk factors associated with it. The aim of this study was to identify the factors associated with early death in community-acquired pneumonia patients. Methods : From January 1999 to July 2004, 1,487 adult patients with community-acquired pneumonia who were admitted to the pulmonary department via emergency center were examined. Early death was defined as those who died within 2 days of hospitalization. The clinical and laboratory aspects of the patients who died early (n = 30) were compared with those of an age and gender matched control population (n = 60) . Results : In the early death group, respiratory rate, heart rate, and blood urea nitrogen (BUN) were significant higher (p < 0.05 for all), while the arterial pH, systolic pressure, and PaO2 were significant lower (p < 0.05 for all) than the control. The independent factor significantly associated with early death was tachypnea (OR, 7.049). Conclusion : The importance of an early clinical assessment in emergency center with community-acquired pneumonia needs to be emphasized in order to recognize patients at risk of early death. (Tuberc Respir Dis 2005; 58: 607-613)
저자들은 자궁근종으로 자궁적출술을 시행받은 과거력이 있는 35세 여자환자가 우연히 발견된 폐의 다발성 결절을 주소로 내원한 후, 폐 생검을 통하여 양성 전이성 폐 평활근종을 진단받고, 이후 개흉술을 통한 전 결절 제거술을 성공적으로 시행 받은 드문 1 예를 경험하였고, 이는 국내에서는 처음 시도된 바이기에 문헌고찰과 함께 보고하는 바이다.
A benign metastasizing pulmonary leiomyoma (BMPL) is a rare disease that usually occurs in women with a prior or coincident history of uterine leiomyoma. Although leiomyoma is histologically benign, it has the potential to metastasize to a distant site such as the lung. A 35 year old woman who had undergone a hysterectomy due to uterine leiomyoma 5 years prior was admitted for an investigation of multiple pulmonary nodules on a routine chest roentgenogram. An open lung biopsy was taken to make a pathological diagnosis. The microscopic finding of the nodules was leiomyoma and was similar to those of the uterine leiomyoma that had been resected 5 years ago. The woman underwent wedge resections of all pulmonary nodules. This is the first case of BMPL in Korea, which was treated with wedge resections of all multiple pulmonary nodules. (Tuberc Respir Dis 2005; 58: 614-618)
Blastomycosis is a systemic pyogranulomatous disease that is caused by a thermally dimorphic fungus, Blastomyces dermatitidis. it’s the disease is endemic in the south-eastern and south central states of the USA, which border the Mississippi and Ohio Rivers, the mid-western states and Canadian provinces bordering the Great Lakes as well as in a small area of New York and Canada adjacent to the St. Lawrence River.1 We encountered a case of blastomycosis, representing as a pulmonary manifestation after traveling around a non- endemic area and report it with a brief review of the relevant literature. (Tuberc Respir Dis 2005; 58: 619-623)