• Korean Journal of Radiology
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• 제22권10호
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• pp.1719-1729
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• 2021

Objective: Emphysema and small-airway disease are the two major components of chronic obstructive pulmonary disease (COPD). We propose a novel method of quantitative computed tomography (CT) emphysema air-trapping composite (EAtC) mapping to assess each COPD component. We analyzed the potential use of this method for assessing lung function in patients with COPD. Materials and Methods: A total of 584 patients with COPD underwent inspiration and expiration CTs. Using pairwise analysis of inspiration and expiration CTs with non-rigid registration, EAtC mapping classified lung parenchyma into three areas: Normal, functional air trapping (fAT), and emphysema (Emph). We defined fAT as the area with a density change of less than 60 Hounsfield units (HU) between inspiration and expiration CTs among areas with a density less than -856 HU on inspiration CT. The volume fraction of each area was compared with clinical parameters and pulmonary function tests (PFTs). The results were compared with those of parametric response mapping (PRM) analysis. Results: The relative volumes of the EAtC classes differed according to the Global Initiative for Chronic Obstructive Lung Disease stages (p < 0.001). Each class showed moderate correlations with forced expiratory volume in 1 second (FEV₁) and FEV₁/forced vital capacity (FVC) (r = -0.659-0.674, p < 0.001). Both fAT and Emph were significant predictors of FEV₁ and FEV₁/FVC (R² = 0.352 and 0.488, respectively; p < 0.001). fAT was a significant predictor of mean forced expiratory flow between 25% and 75% and residual volume/total vital capacity (R² = 0.264 and 0.233, respectively; p < 0.001), while Emph and age were significant predictors of carbon monoxide diffusing capacity (R² = 0.303; p < 0.001). fAT showed better correlations with PFTs than with small-airway disease on PRM. Conclusion: The proposed quantitative CT EAtC mapping provides comprehensive lung functional information on each disease component of COPD, which may serve as an imaging biomarker of lung function.

• Tuberculosis and Respiratory Diseases
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• 제65권6호
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• pp.457-463
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• 2008

연구배경: 호기말에 흉부 촬영을 시행하면 폐 내의 공기의 부피가 감소되어 폐 감쇄도가 증가한다. 이런 폐 감쇄도의 변화가 국소적으로 저하되는 공기 가둠 현상에 대해서는 일부 연구들이 있었으나 전체 폐의 전반적인 감쇄도 변화에 대한 연구는 거의 없고, 특히 정상인을 대상으로 한 연구는 거의 없다. 저자들은 호흡기 질환이 없으며 폐기능 및 흡기 전산화단층촬영이 정상 소견이고 호기 영상에서 국소적인 공기 가둠 현상이 없는 100명을 대상으로 연구를 수행하였다. 방 법: 흉부 전산화단층촬영 영상에서 24개의 지점을 정하고, 흡기 및 호기 시 각 지점에서 폐 음영도를 측정한 후 호기말 폐 감쇄도 증가와 흡연량, 연령 사이의 상관 관계를 알아보았다. 결 과: 연구 대상 100명의 연령은 중앙값 49.0세(범위 25~71세)였고, 평균 흡연량은 $22.5{\pm}17.0$갑년이었다. 연령과 폐 감쇄도의 증가 사이에는 유의한 음의 상관관계가 있었으며 이는 흡연의 효과를 보정하였을 때에도 유지되었고, 연령을 기준으로 세 군으로 나누어 폐 감쇄도의 증가 정도를 비교하였을 때에도 유의한 차이가 있었다. 흡연량과 호기말 폐 감쇄도의 증가 사이에는 유의한 음의 상관관계가 관찰되었으나 연령을 보정하였을 때에는 유의성이 감소하였다. 결 론: 흡기-호기 시의 폐의 전반적인 감쇄도 변화 정도는 연령과 상관관계가 있으며, 노화를 반영할 가능성이 있다.

• 대한한방내과학회지
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• 제29권2호
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• pp.529-534
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• 2008

Renal cell carcinoma(RCC) is one of the major malignant renal cell tumors. Although RCC can metastasize to almost every organ, the most common metastatic sites are the lung parenchyma, the bones, the liver, and the brain. Adrenal metastasis from RCC is extremely rare. Adrenal metastasis from RCC shows poor prognosis, with little benefit from chemotherapy, radiation therapy, hormone therapy or immunotherapy. In this report, we describe a case of an RCC patient who showed lung and adrenal metastasis. The patient underwent left nephrectomy and chemotherapy(sunitinib), which were not effective. He refused further conventional medical treatment, and instead started treatment with Traditional Korean Medicine using allergen-removed Rhus verniciflua Stokes. After about 3 months of this treatment, the size of the adrenal tumor had decreased significantly with good performance status. Further study will be needed to demonstrate the tumor regression effect of allergen-removed Rhus verniciflua Stokes on patients with metastatic renal cell carcinoma.

• Tuberculosis and Respiratory Diseases
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• 제57권4호
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• pp.381-385
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• 2004

저자들은 클렙시엘라균종에 의한 폐렴에 동반된 폐 괴저를 수술적 치료없이 약물로만 호전시킨 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제32권3호
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• pp.246-250
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• 2010

Mediastinal emphysema, also referred to as pneumomediastinum or Hamman's syndrome, is defined as the presence of air or gas within the fascial planes of the mediastinum. Superior extension of air into the cervicofacial subcutaneous space via communications between the mediastinum and cervical fascial planes or spaces occurs occasionally. The mediastinal air may originate from the respiratory tract, the intrathoracic airway, the lung parenchyma, or the gastrointestinal tract. The presence of air in the mediastinum may be spontaneous, iatrogenic or due to penetrating trauma. Pneumothorax is defined as the presence of air or gas within the pleural cavity. A pneumothorax can occur spontaneously. It can also occur as the result of a disease or injury to the lung or due to a puncture to the chest wall. Pneumomediastinum and pneumothorax is a rare complication of head and neck surgery. Nevertheless, when it occurs, it is usually considered to result from direct dissection by the air at the time of injury or of surgery. Most of the cases of pneumomediastinum and pneumothorax that have been described in the oral and maxillofacial surgery literature result from air dissecting down the fascial planes of the neck. The authors report a case with subcutaneous emphysema, pneumomediastinum and pneumothorax after orthognathic surgery.

• Journal of Chest Surgery
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• 제46권3호
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• pp.197-201
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• 2013

Background: Most traumatic tracheobronchial injuries are fatal and result in death. Some milder cases are not life threatening and are often missed at the initial presentation. Tracheobronchial rupture is difficult to diagnose in the evaluation of severe multiple trauma patients. We reviewed the traumatic tracheobronchial injuries at Konyang University and Eulji University Hospital and analyzed the clinical results. Materials and Methods: From January 2001 to December 2011, 23 consecutive cases of traumatic tracheobronchial injury after blunt trauma were reviewed retrospectively. We divided them into two groups by the time to diagnosis: group I was defined as the patients who were diagnosed within 48 hours from trauma and group II was the patients who diagnosed 48 hours after trauma. We compared the clinical parameters of the two groups. Results: There was no difference in the age and gender between the two groups. The most common cause was traffic accidents (56.5%). The Injury Severity Score (ISS) was 19.6 in group I and 27.5 in group II (p=0.06), respectively. Although the difference in the ISS was not statistically significant, group II tended toward more severe injuries than group I. Computed tomography was performed in 22 cases and tracheobronchial injury was diagnosed in 5 in group I and 6 in group II, respectively (p=0.09). Eighteen patients underwent surgical treatment and all four cases of lung resection were exclusively performed in group II (p=0.03). There were two mortality cases, and the cause of death was shock and sepsis. Conclusion: We believe that close clinical observation with suspicion and rigorous bronchoscopic evaluation are necessary to perform diagnosis earlier and preserve lung parenchyma in tracheobronchial injuries from blunt trauma.

• Journal of Yeungnam Medical Science
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• 제34권2호
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• pp.279-284
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• 2017

Pulmonary artery sarcoma (PAS) is a rare and fatal disease that often mimics chronic thromboembolic pulmonary hypertension (CTEPH); therefore, diagnosis of PAS is often delayed. Herein, a healthy 74-year-old man was presented with a 4-month history of dyspnea. Chest computed tomography showed wall thickening and stenosis in the main pulmonary artery as well as in both proximal pulmonary arteries. In order to differentiate between unusual CTEPH, vasculitis, and PAS, we performed right heart catheterization and pulmonary angiography. The mean pulmonary arterial pressure was 21 mmHg, and there was severe pulmonary artery stenosis. Thrombi on the pulmonary arterial wall lesions were observed in intravascular ultrasound and optical coherence tomography. Furthermore, the patient had a history of deep vein thrombosis. Therefore, we diagnosed unusual CTEPH. After 6 months of rivaroxaban anticoagulation therapy, a chest X-ray revealed a left lower lobe lung mass, and a positron emission tomography later showed hypermetabolic lesions in the main pulmonary artery wall, in both pulmonary arteries walls, in the lung parenchyma, and in the bones. A biopsy of the right proximal humerus lesion revealed undifferentiated intimal sarcoma. Pulmonary sarcoma is rare, but should be considered when differentially diagnosing main pulmonary artery wall thickening and stenosis. A positron emission tomography may aid in this diagnosis.

• Journal of Chest Surgery
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• 제41권2호
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• pp.281-284
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• 2008

기관지 내 이물은 대부분 흡입에 의해서 발생한다. 하지만 본 증례에서는 폐엽 절제술을 시행받은 5년 후, 기관지 내로 수술 시 사용한 비금속성 이물질이 배출된 드문 경우이다. 이 기관지 이물은 기관지 내시경으로 제거되었으며 수술 중 지혈 목적으로 사용된 테플론으로 밝혀졌다. 아직 수술 후 이러한 이물들이 기관지로 이주하여 배출되는 정확한 원인은 알 수 없으나 이번 증례는 일본에서 발표된 증례와 함께 비금속성의 물질들도 폐 실질에서 기관지로의 이주가 가능하다는 증거가 된다는 점에서 의미가 있겠다.

• Tuberculosis and Respiratory Diseases
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• 제48권4호
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• pp.550-555
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• 2000

폐격리증은 비정상적으로 발생한 폐조직과 이상동맥에 의해 형성된 선천성 질환으로 비교적 드문질환이다. 폐격리증에서 이상동맥의 해부학적 위치는 수술합병증의 발생에 매우 중요하다. 저자들은 객혈을 주소로 내원한 61세 남자환자에서 대동맥촬영상 좌위동맥에서 기시하는 비비꼬인 형태의 이상동맥에 의해 공급받는 폐격리증 1예를 경험하였기에 보고하는 바이다.

• Tuberculosis and Respiratory Diseases
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• 제51권5호
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• pp.466-473
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• 2001

Pulmonary epithelioid hemangioendothelioma (PEH), originally termed an intravacular bronchioloalveolar tumor, is a rare pulmonary neoplasm with a vascular origin and slow rate of malignancy. It affects various organs such as the liver, the central nervous system, lung, etc. Clinically, pulmonary epithelioid hemangioendothelioma has been considered to be a borderline malignancy, a generally indolent and nonaggressive tumor that displaces the pulmonary parenchyma over a number of years by slowly enlarging the tumor nodule. The clinical course of PEH is known to be usually benign. Here we report an unusual case of PEH that was highly malignant and was eventually fatal. The PEH was confirmed by microscopic analysis and immunohistochemical staining of CD31+(a membrane receptor and a sensitive and specific marker for vascular lesions) from an open lung biopsy specimen.