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조직학적 기질성 폐렴 형태인 치유되지 않는 폐렴의 임상적 고찰
박성주 ( Seoung Ju Park ),백경현 ( Kyung Hyun Paeck ),최영훈 ( Yeong Hun Choe ),김소리 ( So Ri Kim ),이용철 ( Yong Chul Lee ),이양근 ( Yang Keun Rhee ),진공용 ( Gong Yong Jin ),이흥범 ( Heung Bum Lee ) 대한내과학회 2008 대한내과학회지 Vol.74 No.2
Background/Aims: Non-resolving or slow-resolving pneumonia refers to the persistence of pulmonary infiltrates for >30 days after an initial pneumonia-like illness. Organizing pneumonia (OP) can be found on a lung biopsy in association with a number of diseases. The object of this study was to elucidate the clinical characteristics of the non-resolving pneumonia with the pathology of an OP and suggest the proper diagnostic and therapeutic approaches for the reduction of unnecessary procedures. Methods: We retrospectively analyzed 70 patients diagnosed with an OP by percutaneous transthoracic needle biopsy and that met the inclusion criteria. Their pulmonary lesions were reviewed for disease resolution. Patients were divided into either a radiologically benign group (group I, n=57) or a malignancy group (group II, n=13) based on the computed tomography (CT) findings. Results: All patients in group I and 8 patients in group II improved and had a complete resolution by 81.70±45.36 days. The microbiology findings showed that many infectious pathogens can lead to an OP despite antibiotic therapy. Three cases in group II were ultimately diagnosed as malignancies. Conclusions: Our data suggest that non-resolving or slow-resolving lesions were strongly suspicious for a malignancy on the CT scans, despite appearing to be benign OP pathologically; such cases should be considered for re-biopsy. In cased with pathology consistent with OP and benign CT findings, careful observation for 3 months is recommended to allow for the complete radiological resolution of the benign OP associated with infection.
Bleomycin 유도 폐 섬유화 쥐 모델에서 미세 전산화단층촬영의 유용성
이재아 ( Jae A Lee ),진공용 ( Gong Yong Jin ),복세미 ( Se Mi Bok ),한영민 ( Young Min Han ),박성주 ( Seoung Ju Park ),이용철 ( Yong Chul Lee ),정명자 ( Myung Ja Chung ),윤건하 ( Gun Ha Youn ) 대한결핵 및 호흡기학회 2009 Tuberculosis and Respiratory Diseases Vol.67 No.5
Background: Micro computed tomography (CT) is rapidly developing as an imaging tool, especially for mice, which have become the experimental animal of choice for many pulmonary disease studies. We evaluated the usefulness of micro CT for evaluating lung fibrosis in the murine model of bleomycin-induced lung inflammation and fibrosis. Methods: The control mice (n=10) were treated with saline. The murine model of lung fibrosis (n=60) was established by administering bleomycin intra-tracheally. Among the 70 mice, only 20 mice had successful imaging analyses. We analyzed the micro CT and pathological findings and examined the correlation between imaging scoring in micro CT and histological scoring of pulmonary inflammation or fibrosis. Results: The control group showed normal findings on micro CT. the abnormal findings on micro CT performed at 3 weeks after the administration of bleomycin were ground-glass opacity (GGO) and consolidation. At 6 weeks after bleomycin administration, micro CT showed various patterns such as GGO, consolidation, bronchiectasis, small nodules, and reticular opacity. GGO (r=0.84) and consolidation (r=0.69) on micro CT were significantly correlated with histological scoring that reflected pulmonary inflammation (p<0.05). In addition, bronchiectasis (r=0.63) and reticular opacity (r=0.83) on micro CT shown at 6 weeks after bleomycin administration correlated with histological scoring that reflected lung fibrosis (p<0.05). Conclusion: these results suggest that micro CT findings from a murine model of bleomycin-induced lung fibrosis reflect pathologic findings, and micro CT may be useful for predicting bleomycin-induced lung inflammation and fibrosis in mice.
폐혈색전증에 의한 급성신부전을 동반한 다발성 대칭성 지방종증 1 예
이나리(Na Ri Lee),진흥용(Heung Yong Jin),박성주(Seoung Ju Park),윤일용(Il Yong Yun),권혁진(Hyeok Jin Kwon),문치영(Chi Young Moon),김원(Won Kim),박성광(Sung Kwang Park),강성귀(Sung Kyew Kang) 대한내과학회 2002 대한내과학회지 Vol.62 No.5
Multiple symmetric lipomatosis (MSL) is a rare disease characterized by the presence of diffuse, non-tender, symmetric deposits of adipose tissue on the neck, back and upper part of the trunk. It has been reported that this disease could be associated with various metabolic abnormalities such as impaired glucose tolerance, hyperuricemia, alcohol consumption, type 4 hyperlipidemia, renal tubular acidosis and thyroid disorder. We present a case of type 2 MSL with pulmonary thromboembolism. He suffered sudden dyspnea and decreased urine output. The causes of dyspnea and acute renal failure (ARF) in this case were dehydration and hemodynamic disturbance due to pulmonary thromboembolism. After thrombolytic and fluid therapy, his condition was improved. He was discharged on warfarin medication and has remained asymptomatic for 12 months.(Korean J Med 62:575-580, 2002)
증예(症例) : Kartagener 증후군 환자의 급성호흡부전-비침습적 환기치료로 호전된 1예
백경현 ( Kyung Hyun Paeck ),홍윤경 ( Yun Kyung Hong ),이가영 ( Ka Young Lee ),김소리 ( So Ri Kim ),민경훈 ( Kyung Hoon Min ),박성주 ( Seoung Ju Park ),이홍범 ( Heung Bum Lee ),이용철 ( Yong Chul Lee ),이양근 ( Yang Keun Rhee ) 전북대학교 의과학연구소 2006 全北醫大論文集 Vol.30 No.1
Kartagener 중후군 환자에서 급성호흡부전이 발생할 경우, 원인이 되는 호흡기 감염과 염증을 조기에 치료하고 이에 더불어 발생하는 심각한 호흡부전상태를 해결하기 위해 기관내 삽관을 통한 침습적 기계호흡을 대신하여 비침습적 양압환기를 시도해 볼 수 있다. 이러한 비침습적 양압환기는 효과적으로 적절한 가스 교환과 호흡근의 휴식을 가능하게 하여 생존율을 향상시키며, 반복되는 기관내 삽관 또는 기관절개술로 인한 합병증을 줄이고 언어, 식사 등의 일상생활을 가능하게 하여 삶의 질을 향상시킬 수 있는 장점을 가진다. 효과적인 비첨습적 양압환기를 위해서는 적절한 마스크의 선택과 정확한 착용이 중요하고 환자의 교육과 격려가 필요하다. 저자들은 Kartagener 증후군으로 치료받던 환자에서 폐렴과 동반되어 발생한 급성호흡부전을 항생제 치료와 함께 흡기시 양기도압과 호기시 양기도압을 조절하는 자발호흡 방식의 비첨습적 양압환기를 시행하여 성공적으로 치료하였기에 문헌 고찰과 함께 증례를 보고하는 바이다. Kartagener`s syndrome is characterized by the triad of situs inversus, bronchiectasis, and chronic pansinusitis. With pulmonary infection such as pneumonia or other certain conditions, pulmonary symptoms of Kartagener`s syndrome are aggravated and hypoventilation and hypercapnia are exacerbated. These conditions may induce acute respiratory failure (ARF). Noninvasive positive pressure ventilation (NPPV) is well tolerated and safe, and it has assumed a prominent role in the management of ARF. The attraction for NPPV relates primarily to its advantages over invasive mechanical ventilation. It is used in patients with ARF due to exacerbations in chronic obstructive pulmonary disease or cardiogenic pulmonary edema. We report a case that ARF in a patient with kartagener`s syndrome is successfully treated with NPPV.