• Tuberculosis and Respiratory Diseases
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• 제69권4호
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• pp.293-297
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• 2010

A 60-year-old man was diagnosed with stage IV squamous cell carcinoma of lung and treated with weekly doses of docetaxel and cisplatin. Tumor mass and mediastinal lymphadenopathy disappeared after 4.5 cycles of chemotherapy. At one week post final chemotherapy, the patients developed sudden shortness of breath. New, multifocal infiltrations developed on both lungs without definitive evidence of infection. Despite administration of broad spectrum antibiotics, the lung lesion did not improve, so bronchoalveolar lavage and computed tomography-guided lung biopsy were performed. The proportion of lymphocytes was increased markedly and histopathology revealed squamous cell carcinoma combined with bronchiolitis obliterans organizing pneumonia. After high dose corticosteroid therapy, dyspnea and the newly developed consolidation had decreased slightly. However, dyspnea and hypoxemia increased again because of aggravated lung cancer since chemotherapy had stopped. Chemotherapy couldn't be restarted due to the poor performance status of the patient. Later, patient died of respiratory failure from poor general condition and progression of lung cancer.

• Tuberculosis and Respiratory Diseases
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• 제78권3호
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• pp.190-195
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• 2015

Background: Although organizing pneumonia (OP) responds well to corticosteroid therapy, relapse is common during dose reduction or follow-up. Predictors of relapse in OP patients remain to be established. The aim of the present study was to identify factors related to relapse in OP patients. Methods: This study was retrospectively performed in a tertiary referral center. Of 66 OP patients who were improved with or without treatment, 20 (30%) experienced relapse. The clinical and radiologic parameters in the relapse patient group (n=20) were compared to that in the non-relapse group (n=46). Results: Multivariate analysis demonstrated that percent predicted forced vital capacity (FVC), $PaO_2/FiO_2$, and serum protein level were significant predictors of relapse in OP patients (odds ratio [OR], 0.82; 95% confidence interval [CI], 0.70-0.97; p=0.018; OR, 1.02; 95% CI, 1.00-1.04; p=0.042; and OR, 0.06; 95% CI, 0.01-0.87; p=0.039, respectively). Conclusion: This study shows that FVC, $PaO_2/FiO_2$ and serum protein level at presentation can significantly predict relapse in OP patients.

• Journal of Chest Surgery
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• 제47권4호
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• pp.420-422
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• 2014

A 44-year-old pregnant female patient gave stillbirth while being treated for pneumonia. She developed acute respiratory failure, which resulted in mechanical ventilator support. Diagnostic lung biopsy revealed a cryptogenic organizing pneumonia. The patient's condition deteriorated and a venous-venous extracorporeal membrane oxygenation was placed. She was listed for lung transplantation. Because of her worsening condition lung transplantation was performed despite positive cross matching result. She was treated with rituximab, intravenous immunoglobulin, and plasmapheresis and recovered without event. There is no sign of rejection at the time of last follow-up.

• Tuberculosis and Respiratory Diseases
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• 제82권4호
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• pp.269-276
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• 2019

Idiopathic interstitial pneumonia (IIP) is a histologically identifiable pulmonary disease without a known cause that usually infiltrates the lung interstitium. IIP is largely classified into idiopathic pulmonary fibrosis, idiopathic non-specific interstitial pneumonia, respiratory bronchiolitis-interstitial lung disease (ILD), cryptogenic organizing pneumonia, desquamative interstitial pneumonia, and acute interstitial pneumonia. Each of these diseases has a different prognosis and requires specific treatment, and a multidisciplinary approach that combines chest high-resolution computed tomography (HRCT), histological findings, and clinical findings is necessary for their diagnosis. Diagnosis of IIP is made based on clinical presentation, chest HRCT findings, results of pulmonary function tests, and histological findings. For histological diagnosis, video-assisted thoracoscopic biopsy and transbronchial lung biopsy are used. In order to identify ILD associated with connective tissue disease, autoimmune antibody tests may also be necessary. Many biomarkers associated with disease prognosis have been recently discovered, and future research on their clinical significance is necessary. The diagnosis of ILD is difficult because patterns of ILD are both complicated and variable. Therefore, as with other diseases, accurate history taking and meticulous physical examination are crucial.

• Tuberculosis and Respiratory Diseases
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• 제71권5호
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• pp.368-372
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• 2011

Acute fibrinous and organizing pneumonia is a newly recognized pattern of acute lung injury. A 49-year-old female presented with a cough and worsening dyspnea on exertion. She had no history of smoking and no specific past medical history except exposure of home humidifier containing sterilizer. A chest computed tomography scan showed patchy consolidation with fibrosis in the right lower lobe and ill-defined centrilobular ground glass opacity in both lungs. The pathological findings were patchy areas of lung parenchyma with fibrin deposits in the alveolar ducts and alveoli, and fibrin balls with hemosiderin deposition in the alveolar spaces. The histological pattern of our case is differentiated from diffuse alveolar damage by the absence of hyaline membranes, and from eosinophilic pneumonia by the lack of eosinophils. In our case, the patient was treated with corticosteroid pulse therapy. However, the clinical course became aggravated and she died within two weeks.

• Tuberculosis and Respiratory Diseases
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• 제46권5호
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• pp.709-717
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• 1999

연구배경 및 방법 : BOOP는 미만성 간질성 폐질환의 일종으로 기질화폐렴의 특별한 한 형태로도 구분되는 아주 특별한 임상병리 소견을 가진 질환이다. 임상적으로는 내원 수주전부터 감기 유사증상을 앓다가 점차 악화되는 호흡곤란 증세로 내원하여 마치 폐렴양 소견을 보이며, 병리학적으로 폴립형의 육아 조직이 세기관지내에 충전되어 관강내 용종양 조직을 형성하고 폐포관에까지 침범된 기질화된 폐렴의 소견을 보인다. 최근, 저자등은 본원에서 경험한 다섯 증례와 국내의 학술지상에 증례 보고된 19예를 합하여 그 임상적 특성에 대해 분석해 보고 국외의 문헌보고 결과들과 비교분석하고자 하였다. 결 과 : 국내 환자들의 평균연령은 54세이었으며 여성에서 약간 더 많이 발생하였다. 병원에 내원한 주증상은 호흡 곤란 및 기침이었으며 그 지속기간은 평균 41일이었다. 흉부진찰에서 흡기시 악설음이 흔히 관찰되었고 여러 혈액학적 검사소견은 저산소혈증외에는 비특이적이었으며 이들 소견만으로는 폐렴과 구분하기 어려웠다. 폐활량검사에서는 제한성 혹은 폐쇄성과의 혼재형 환기장애가 주소견이었으며 방사선학적으로는 양측성, 반상의 비엽성 폐포침윤을 보였고 고해상 컴퓨터단층촬영에서 잘 확인되었다. 다른 간질성폐질환과는 달리 부신피질호르몬의 치료에 잘 반응하여 양호한 예후 및 경과를 보였다. 상기 국내의 결과는 국외 문헌보고에서 얻은 결과와 비교시에 대체적으로 유사 소견을 보였으나 국내는 여자에서 더 흔히 발생한 차이가 있었으며 엑스선 소견 및 임상경과 등에 대해서는 좀더 추적조사를 하여 비교해야 할 것으로 판단된다. 결 론 : 폐렴양 소견을 보이는 환자에서 적절한 치료에도 불구하고 임상양상이 비전형적이고 진행시에는 임상소견 및 방사선학적 소견 등을 BOOP의 관점에서 재점검해야 할 것이다. 이 질환은 부신피질호르몬제에 비교적 빠른 반응을 보이며 조기 진단으로 완치가 가능하지만 성급한 치료종결시 재발이 잘 되며 급격한 호흡부전으로 사망할 수도 있는 질환이므로 BOOP가 의심되고 치료에도 병이 진행성일 때 적기에 조직검사를 통해 확진함이 중요하다.

• Tuberculosis and Respiratory Diseases
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• 제68권3호
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• pp.175-179
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• 2010

The ulcerative colitis is a chronic inflammatory bowel disease with an unknown etiology. The major symptoms of ulcerative colitis are diarrhea, abdominal pain and hematochezia. However, arthritis, skin disorders, hepatobiliary inflammation and uveitis are occasionally recognized as systemic complications. Although there are few reports of coexistent pulmonary and inflammatory bowel disease, the lung is not generally considered to be a target organ in ulcerative colitis. We report a patient with ulcerative colitis-related bronchilolitis obliterans organizing pneumonia confirmed by video-assisted thoracoscopic surgery, who responded to corticosteroid therapy.

• Tuberculosis and Respiratory Diseases
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• 제70권1호
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• pp.43-50
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• 2011

Background: Open lung biopsy is used for diagnosis of diffuse infiltrative lung diseases (DILD), but it is invasive and relatively expensive procedure. Fluoroscopy-guided cutting needle lung biopsy (FCNLB) has merits of avoidance of admission and rapid diagnosis. But diagnostic accuracy and safety were not well known in the diagnosis of DILD. Methods: We included 52 patients (37 men, 15 women) having DILD on HRCT with dyspnea, except the patients who could be confidently diagnosed with clinical and HRCT findings. FCNLB was performed using 16G Ace cut needle (length 1.5 cm, diameter 2 mm) at the area of most active lesion on HRCT. Final diagnoses were made by the consensus. Results: The mean interval between the HRCT and FCNLB was 4.5 days. Most cases were performed one biopsy during 5~10 minutes. Specific diagnosis was obtained in 43 of 52 biopsies (83%). The most common diagnosis was nonspecific interstitial pneumonia (11 cases) and followed by cryptogenic organizing pneumonia (7 cases), diffuse alveolar hemorrhage and usual interstitial pneumonia (5 cases in each), hypersensitivity pneumonitis (3 cases), tuberculosis and drug induced interstitial pneumonitis (2 cases in each), the others are in one respectively. Mild complication was developed in 9 patients (8 pneumothorax, 1 hemoptysis). Most of complications were regressed without treatment except one case with chest tube insertion for pneumothorax. Conclusion: Fluoroscopy-guided 16 G cutting needle lung biopsy was an useful method for the diagnosis of DILD.

• Tuberculosis and Respiratory Diseases
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• 제66권2호
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• pp.141-151
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• 2009

연구배경: 과거 국내외 특발성 간질성 폐렴(IIP)의 역학 조사는 제한적이었다. 간질성 폐질환에 대한 관심이 증가하고 있고 국내 IIP 환자들의 분포 및 역학에 대해서 알려진 바 없어 이를 알아보고자 하였다. 방 법: 2003년 1월 1일부터 2007년 12월 31일 사이에 진단된 환자들을 대상으로 하였으며, 진단은 ATS/ERS 기준에 따랐다. 결 과: 입력된 환자는 3,156명이었으나, 중복, 진단기준 미달, 부정확한 자료로 970명이 제외되어 총 2,186명을 분석하였다. 남녀 비는 약 2 : 1이었고 이들의 평균 나이는 65세(11-94세)였다. 빈도는 특발성 폐 섬유화증(IPF) 1,685명(77.1%), 비특이적 간질성 폐렴(NSIP) 261명(11.9%), 특발성 기질화 폐렴(COP) 186명(8.5%), 급성 간질성 폐렴(AIP) 24명(1.1%), 박리성 간질성 폐렴(DIP) 19명(0.9%), 호흡성 세기관지염-간질성 폐질환(RB-ILD) 9명(0.4%), 림프구성 간질성 폐렴(LIP) 2명(0.1%)였다. 평균 나이는 IPF 67.8세, COP 57.7세, NSIP 57.1세로 IPF 환자의 나이가 가장 많았다. 전체 환자를 대상으로 하였을 때, 운동 시 호흡곤란은 68.9%, 기침 60.8%, 객담 32.5%, 흉통 6.8%, 객혈 2.2%, 무증상 4.5%로 운동 시 호흡곤란의 증상이 가장 많았다. IPF의 3년 생존율은 62%였고, NSIP와 COP의 5년 생존율은 모두 85%였다. 결 론: 이 조사는 국내의 IIP 치료 및 진료 지침을 제작에 유용한 도움을 줄 것으로 판단된다.