• 제목/요약/키워드: Lung biopsy

검색결과 619건 처리시간 0.04초

폐암의 전국 실태 조사 (The National Survey of Lung Cancer in Korea)

  • 대한결핵 및 호흡기학회 학술위원회
    • Tuberculosis and Respiratory Diseases
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    • 제46권4호
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    • pp.455-465
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    • 1999
  • 연구배경: 최근 급증하는 폐암에 대해 국내에서는 단위 병원의 폐암 환자의 특성, 조직학적 분류에 따른 분포, 진단 방법, 치료방법에 대한 수년간의 통계들이 있을 뿐 전국적인 조사는 없어 전국적인 폐암환자의 기초자료의 필요성이 대두되었다. 방 법: 대한 결핵 및 호흡기 학회에서는 전국을 대상으로 1997년 1년 동안 조직학적으로 증명된 원발성 폐암환자를 대상으로 환자의 특성, 폐암의 조직학적 분류, 병기, 치료법 등 폐암의 특성을 조사하였다. 결 과: 총 3,794명을 분석하여 다음의 결과를 얻었다. 1) 남자 환자가 79.3%였으며 평균 연령은 62.0세(남자 62.2세, 여자는 61.6세)였으며 76.8%가 흡연자로 남자환자의 89.8%, 그리고 여자환자의 25.4%가 흡연자이었다. 2) 병리학적으로는 편평상피세포암이 44.7%, 선암 27.9%, 기관지폐포세포암 2.2%, 대세포폐암 1.5%, 소세포폐암 16.8%로 관찰되었다. 흡연력은 편평상피세포암의 87.5%, 선암의 56.2%, 기판지폐포세포암의 35.5%, 대세포폐암의 94.1% 및 소세포폐암의 84.3%가 흡연자였으며 편평상피세포폐암 및 소세포폐암 환자에 비해 선암 환자의 흡연자 비율이 유의하게 낮았다(p<0.001). 3) 조직학적 진단방법은 객담세포진 검사가 15.5%, 기관지내시경을 통한 조직검사가 44.4%, 경피적 폐침생검법이 19.7%으로 중심형 암인 편평상피세포암 및 소세포암 환자에서는 기관지내시경 조직검사로 가장 많이 진단이 이루어진 반면 선암 및 대세포폐암 환자에서는 경피적 폐침생검법으로 진단이 많이 이루어졌다(p<0.001). 4) 환자의 진단시 증상은 기침 57.2%, 객담 40.8%, 호흡곤란 35.4%에서 보고되었으며 증상이 없었던 경우도 7.2%이었다. 5) 비소세포폐암환자 임상적 병기는 제I기 13.7%, 제II기 4.5%, 제IIIA기 16.6%, 제IIIB기 28.8% 및 제IV기 36.5%로 진행되어 발견되는 경우가 많았다. 소세포폐암환자 609명 중 제한병기가 45.2%, 확대병기가 54.8%이었다. 결 론: 폐암은 남자 및 흡연자에서 주로 발생하였으며 편평상피세포암이 가장 많았다. 따라서 이러한 국내의 자료는 폐암환자에서 여성의 비율이 상대적으로 높고 선암이 가장 흔한 폐암으로 알려진 구미의 자료와는 차이가 있었다. 진행된 상태에서 발견되는 경우가 많아 조기발견 프로그램의 개발 필요성이 제시되었다.

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A Successful Bilateral Lung Transplantation in a Patient with High Panel Reactive Antibody and Positive Cross Matching

  • Bok, Jin San;Jun, Jae Hyun;Lee, Hyun Joo;Park, In Kyu;Kang, Chang Hyun;Yang, Jaeseok;Kim, Young Tae
    • 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.

폐의 림프관평활근종증 1예 (A Case of Lymphangioleiomyomatosis in Lung)

  • 박정은;김현정;우대형;류영하;이관호;정진홍;신경철
    • Journal of Yeungnam Medical Science
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    • 제27권1호
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    • pp.63-68
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    • 2010
  • Lymphangioleiomyomatosis (LAM) is a rare, cystic lung disease that is associated with mutation in the tuberous sclerosis genes, renal angiomyolipomas, lymphatic spread and a remarkable female gender predilection. The pathology of LAM is represented by the proliferation of immature smooth muscle cells in the walls of airways, and venules and lymphatic vessels in the lung. The clinical course of LAM is characterized by progressive dyspnea on exertion, recurrent pneumothorax and collections of chylous fluid. The diagnosis of pulmonary LAM can be made on chest X-ray, a high-resolution CT scan and lung biopsy. We experienced a case of pulmonary lymphangioleiomyomatosis in a 28-years-old female patient who had suffered from progressive dyspnea on exertion, so we report on it along with a brief review of the relevant literature.

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Glandular papilloma of the lung with malignant transformation

  • Sung, Woo Jung
    • Journal of Yeungnam Medical Science
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    • 제34권2호
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    • pp.298-302
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    • 2017
  • Glandular papilloma of the lung is one of three histologic types of solitary endobronchial papillomas. It is known as an uncommon benign neoplasm. No malignant glandular papillomas have been reported. Herein, the first case of granular papilloma with malignant transformation is reported. A 74-year-old man with huge right lung mass extended upper and lower lobe was admitted to the hospital complaining of progressive cough and dyspnea. An open lung biopsy was performed. Microscopically, the tumor showed papillary growth pattern with thick fibrovascular cores. The stroma of the fibrovascular cores shown the infiltration of lymphoplasmacytic cells and proliferation of capillaries. The epithelial cells surrounding the papillary fronds were cilliated columnar cells with focal cellar atypia, and frequent mitoses. Suspicious pleural invasion foci were identified. The Ki-67 labeling index was about 24.3% and p53 labeling index was about 31.7%. Glandular papilloma is known as a benign neoplasm, which is lack of atypia and mitosis. In present case, there were several indications of malignant transformation, such as cellular atypia, frequent mitosis, architectural distortion, and pleural invasion. Pathologists must be aware that glandular papilloma can have a changes of malignant transformation. Further studies about disease behavior and molecular characteristics are needed.

임신성 융모상피암의 전이성 폐암에 대한 외과적 고찰 (Surgical Management of Metastatic Lung Cancer from Gestational Chorocarcinoma)

  • 정진용
    • Journal of Chest Surgery
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    • 제24권10호
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    • pp.1005-1011
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    • 1991
  • Eighty-four patients with pulmonary metastases from gestational choriocarcinoma were treated at the Catholic Medical Center between August, 1985 and August, 1991. Among these 13 patients underwent thoracotomy with resection of pulmonary lesions and the results obtained were follows. 1] The ages of the patients ranged from 26 to 47 years, with a mean age of 31 years. 2] The frequency of chemotherapy before operation ranged from zero to 46, with a mean frequency of 13.6. 3] Four patients were operated upon for a solitary metastasis of the lung; 6 patients, for unilateral multiple metastases and 3 patients, for bilateral pulmonary metastases. 4] Eight patients underwent wedge resection; 1 patient, segmentectomy; 2 patients, lobectomy; 3 patients, open lung biopsy. The lung lesions of eleven patients showed hemorrhagic necrosis[among these, 2 patients combined with pulmonary tuberculosis]; one was non-necrotic choriocarcinoma; another one was metastatic lung carcinoma from endocrine cancer of unknown origin. 5] Among twelve patients who had managed with chemotherapy before thoracotomy three patients were in remission; among 13 patients who had undergone thoracotomy 6 patients were in remission. 6] The median survival time of these patients was 25.8 months with 3 postoperative deaths. Subsequently, in the patients with pulmonary metastases from choriocarcinoma, if the primary tumor is under control, there are no other metastases, and the patients should be able to tolerate the planned operation, it is necessary to undergo aggressive thoracotomy for diagnostic purposes; for therapeutic purposes only when the pulmonary lesion is the only remaining source of increased hCG excretion; for reduction of tumor volume to shorten hospitalization or to reduce the quantity of drugs.

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폐에 발생한 원발성 악성 섬유성 조직구종 1예 (A Case of Primary Malignant Fibrous Histiocytoma of the Lung)

  • 김건영;류영근;김희종;김영재;김귀완;장명;김수곤;이광민
    • Tuberculosis and Respiratory Diseases
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    • 제38권1호
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    • pp.59-64
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    • 1991
  • The malignant fibrous histiocytoma was the most common soft tissue sarcoma in late life adult. It was first described in 1964 by 0' Brien and Stout. It's histiogenesis had been considered to be of histiocytic origin. It Involves the extremities, retroperitoneum and trunk. It usually metastasizes to the lung. but primary lung lesion is extremly rare and it's prognosis was poor. We have experienced a case of MFR, which was confirmed by open lung biopsy. So we report a case of MFR of the lung with review of literature.

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주변부 폐암에서 기관지세척액을 이용한 MAGE유전자검사법의 임상적 유용성 (MAGE Gene Expression in Bronchial Washing Fluid in Suspected Parenchymal Lung Cancer)

  • 김규진;최은영;신경철
    • Tuberculosis and Respiratory Diseases
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    • 제72권2호
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    • pp.156-162
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    • 2012
  • Background: The main goal of this study was to evaluate the diagnostic efficacy of reverse transcription-nested polymerase chain reaction (RT-nested PCR) in bronchial washing fluid with MAGE A1-6 common primers for the detection of lung cancers invisible by bronchoscopy. Methods: To determine the expression of MAGE A1-6 gene in 189 lung cancers diagnosed by conventional fluoroscopy-guided lung biopsy and 89 cancer-free controls, RT-nested PCR was performed in bronchial washing specimens. We analyzed MAGE A1-6 RT-nested PCR data according to tumor histology, stage, size, and compared them with cytological data. Results: 189 patients (111 cases in adenocarcinoma, 47 cases in squamous cell carcinoma, 22 cases in small cell lung carcinoma, and 9 cases in other cancers) and 89 benign patients were investigated. The expression of MAGE was performed by nested RT-PCR using common MAGE primer. Among 189 cancer patients, the expression rate of MAGE was 49.2%, and the positive predictive value was 89.4%. However, the expression rate of MAGE in patients with benign lesions was 12.4%. In peripheral lung cancer, the positive rate of MAGE expression was 57.4% in squamous cell carcinoma, 44.1% in adenocarcinoma and 59.1% in small cell lung cancer. Whereas the expression rate of bronchial washing cytology in peripheral lung cancer was 9.0% (p=0.011). Conclusion: MAGE RT-PCR in bronchial washing fluid gave us promising data for the detection of peripheral lung cancer. It could be a useful method for selecting diagnostic tools for peripheral lesions.

11세 남아의 기저세포양 편평상피세포폐암 1례 (A Case of Basaloid Squamous Cell Lung Carcinoma in an 11-year-old Boy)

  • 김년천;김승수;서원석;박경배;박준수;신상만;조현득
    • Clinical and Experimental Pediatrics
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    • 제48권2호
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    • pp.208-211
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    • 2005
  • 저자들은 11세 남아가 내원 1개월 전부터 요통과 3일 전부터 양 하지로의 방사성 동통, 양 하지의 쇠약감을 주소로 본원에 입원하여 방사선학적 검사와 조직학적으로 진단된 기저세포양편평상피세포폐암 1례를 경험하였기에 보고하는 바이다.

자연 소실된 폐포단백증 1예 (A Case of Pulmonary Alveolar Proteinosis with Spontaneous Resolution)

  • 남승범;박광영;이호진;정재욱;최윤희;김효석;김철현;이재철
    • Tuberculosis and Respiratory Diseases
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    • 제63권3호
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    • pp.294-298
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    • 2007
  • 폐포단백증은 폐포에 표면활성제 기원의 인지질이 비정상적으로 다량 침착하는 드문 질병으로 자연 소실에서 호흡부전으로 인한 사망까지 다양한 임상경과를 보인다. 그 원인에 따라 선천성, 특발성, 이차성으로 나눌 수 있는데 GM-CSF의 작용경로의 이상이 중요한 병인으로 여겨지고 있다. 치료의 표준은 기관지 폐포세척술이며, 약 8%정도에서는 자연소실 되는 것으로 보고되었다. 저자들은 진단을 위해 흉강경하 쐐기 절제술을 시행하고 경과 관찰하던 중 자연 소실된 폐포단백증 환자를 경험하였기에 문헌고찰과 함께 이를 보고하는 바이다.

원발성 폐암의 외과적 치료 (Surgical Management of Primary Lung Cancer)

  • 박경신;임승평;이영
    • Journal of Chest Surgery
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    • 제28권6호
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    • pp.591-595
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    • 1995
  • Recently, primary lung cancer has increased markedly in incidence and prevalence in Korea. From January 1986 to June 1993, 86 patients were operated and evaluated at the Department of Thoracic and Cardiovascular Surgery, Chungnam National University Hospital. The results are as follows; 1. There were 79 males and 7 females with the peak incidence of 5th and 6th decades of life[75.6% . The age ranged from 13 to 76[mean 56.6$\pm$10.3 years. 2. Symptoms were cough[47.7% , sputum[25.6% , chest pain or dyspnea[18.6% , and hemoptysis or blood tinged sputum[20.9% in order. Symptoms were frequently encountered before hospitalization, but asymtomatic patients were 12.8% in this study. 3. Methods of diagnostic confirmatiom were bronchoscopic biopsy[55.8% , percutaneous needle aspiration[29.1% , suspicious sputum cytology[1.2% , and open biopsy[14.0% . 4. Histopathologically, squamous cell carcinoma[51.2% was the most frequent cell type and adenocarcinoma[26.7% , large cell carcinoma[8.1% , adenosquamous cell carcinoma[3.5% , and the others in order. And TNM stages were Stage I 40.5%, Stage II 15.5%, Stage IIIa 27.4%, and Stage IIIb 3.6%. 5. Methods of operation were pneumonectomy[25.6% , bilobectomy[5.8% , lobectomy[53.4% , segmentectomy[1.2% , and exploration[14.0% . The overall resectability was 86.0% 6. The operative mortality was 2.3% and postoperative complications developed in 7 cases[8.1% . 7. The postoperative follow-up reveals that the overall cumulative survival rates at 1 year, 2 year, 3 year, 4 year, 5 year were 76%, 62%, 43%, 36%, and 27%, respectively.

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