• Journal of Yeungnam Medical Science
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• 제39권2호
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• pp.153-160
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• 2022

Multicentric Castleman disease (MCD) is an uncommon systemic lymphoproliferative disorder that may cause multiple organ damage. Castleman disease-associated diffuse parenchymal lung disease (DPLD) has not been well studied. A 32-year-old man was referred to our hospital for progressive generalized weakness, light-headedness, and dyspnea on exertion for more than one year. Laboratory evaluations showed profound anemia, an elevated erythrocyte sedimentation rate, and an increased C-reactive protein level with polyclonal hypergammaglobulinemia. Chest radiography, computed tomography (CT), and positron emission tomography-CT scan demonstrated diffuse lung infiltration with multiple cystic lesions and multiple lymphadenopathy. In addition to these clinical laboratory findings, bone marrow, lung, and lymph node biopsies confirmed the diagnosis of idiopathic MCD (iMCD). Siltuximab, an interleukin-6 inhibitor, and glucocorticoid therapy were initiated. The patient has been tolerating the treatment well and had no disease progression or any complications in 4 years. Herein, we report this case of human herpesvirus-8-negative iMCD-associated DPLD accompanied by multiple cystic lesions, multiple lymphadenopathy, and polyclonal hypergammaglobulinemia with elevated immunoglobulin G (IgG) and IgG4 levels. We recommend a close evaluation of MCD in cases of DPLD with hypergammaglobulinemia.

• Journal of Chest Surgery
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• 제41권2호
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• pp.292-294
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• 2008

미만성 폐 골화증은 "폐실질 내에 발생하는 이소성 골 형성"으로 정의되는 매우 드문 질환으로 국내에서는 1예가 보고된 바 있으며, 발병 원인은 아직 뚜렷하게 밝혀지지 않았다. 일반적으로 미만성 폐 골화증은 무증상이어서 부검에 의해 진단되는 경우가 대부분이며, 조직 병리 소견에서 결절성과 수지상 두 가지로 분류된다. 저자들은 기존 질환의 병력이 없는 환자에서 발생한 자발성 기흉의 수술적 치료 후 조직 병리 검사에 의해 진단된 미만성 수지상 폐 골화증 1예를 보고하는 바이다.

• Journal of Yeungnam Medical Science
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• 제21권1호
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• pp.101-107
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• 2004

Diffuse alveolar hemorrhage is a rare but serious and frequently life-threatening complication of a variety of conditions. The first goal in the management of patients with diffuse alveolar hemorrhage is to achieve or preserve stability of the respiratory status. Subsequently, the differential diagnosis is aimed at the identification of a remediable cause of the alveolar hemorrhage. The most common causes of diffuse alveolar hemorrhage with glomerulonephritis are microscopic polyangiitis and Wegener's granulomatosis, followed by Goodpasture syndrome and systemic lupus erythematosus. Microscopic polyangiitis (MPA) is a distinct systemic small vessle vasculitis affecting small sized vessels with few or no immune deposits and with no granulomatosus inflammation. The disease may involve multiple organs such as kidney, lung, skin, joint, muscle, gastrointestinal tract, eye, and nervous system. MPA is strongly associated with antineutrophil cytoplasmic autoantibody (ANCA) that is a useful serological diagnostic marker for the most common form of necrotizing vasculitis. Our report concerns a case of microscopic polyangiitis with diffuse alveolar hemorrhage in a 54-year-old man. He was admitted to our hospital due to dyspnea upon exertion and recurrent hemoptysis. Laboratory findings showed hematuria, proteinuria and deterioration of renal function. In the chest CT scan, diffuse ground glass appearance was seen in both lower lungs. A lung biopsy revealed small vessel vasculitis with intraalveolar hemorrhage and showed a positive reaction to against perinuclear ANCA. The patient was treated with prednisolone and cyclophosphamide. Chest infiltration decreased and hemoptysis and hypoxia improved. He is still being followed up in our hospital with a low dose of prednisolone.

• Tuberculosis and Respiratory Diseases
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• 제44권4호
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• pp.716-728
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• 1997

• Tuberculosis and Respiratory Diseases
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• 제72권4호
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• pp.386-389
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• 2012

Diffuse alveolar damage (DAD) is a histological change in lung tissue, and is generally caused by an acute lung injury, which is characterized by bilateral and widespread damages. Localized DAD occurs very rarely. The causes for DAD are numerous, but the chief cause is acute interstitial pneumonia or acute exacerbation of idiopathic interstitial pneumonia, in cases of idiopathic manifestation. The 82-year-old patient, in this case study, showed a DAD lesion in only 1 lobe. The patient was otherwise healthy, with no previous symptoms of DAD. He was admitted to our medical center owing to localized infiltration, observed on his chest radiograph. Laboratory studies showed no signs of infections. DAD was confirmed by a surgical lung biopsy. The patient received corticosteroid treatment and had gradually improved. We report the case of a patient with localized, idiopathic DAD that cannot be classified as acute interstitial pneumonia or acute exacerbation of idiopathic interstitial pneumonia.

• Tuberculosis and Respiratory Diseases
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• 제43권2호
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• pp.285-290
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• 1996

저자들은 특징적인 임상 증상과 함께 전형적인 흉부 x-선 및 고해상 흉부 전산화 단층 촬영을 보이는 미만성 법세기관지염 환자에서 흉강경을 이용한 폐생검으로 확진하여 erythromycin 소량 투여로 임상적 효과를 얻은 1예를 문헌 고찰과 함께 보고는 바이다.

• Tuberculosis and Respiratory Diseases
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• 제43권5호
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• pp.746-754
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• 1996

목적: 미만성 간질성 폐질환은 공통의 임상 양상, 방사선 소견, 폐기능 장애 소견을 갖는, 무수히 많은 원인 질환들로 구성되어 있어 개흉폐생검 등의 조직학적 진단이 표준으로 받아들여지고 있지만 관혈적 진단 방법이라는 단점이 있다. 고해상도 전산화단층촬영은 해상력을 높이고 음영의 중첩 효과를 최소화함으로써 폐간질의 미세한 변화까지 관찰할 수 있게 하겨 미만성 간질성 폐질환의 진단에 매우 유용한 진단 방법이다. 저자들은 이런 고해상도 전산화단층촬영을 한 환자에서 개흉폐생검을 시행하여 진단 및 치료에 어느 정도의 추가 이익을 얻을 수 있었는지 알아보고자 하였다. 방법: 1988년 3월부터 1994년 7월까지 미만성 간질성 폐질환의 진단적 목적으로 개흉폐생검을 시행한 30예의 환자들을 대상으로 후향적으로 고해상도 전산화단층촬영의 진단과 개흉폐생검외 진단 결과를 비교하고 각 환자들의 치료 방침을 조사하였다. 결과: 고해상도 전산화단층촬영은 28예에서 시행되었는데 이 중 22예(78.6%)에서 특이적 진단이 가능하였고 22예 중 20예에서는 개흉폐생검에 의해 같은 진단으로 확진되었다. 나머지 2예 중 1예는 개흉폐생검 결과가 비특이적이었다. 개흉폐생검은 전체 30예 중 25예(83.3%)에서 특이적 진단을 하였다. 또한 고해상도 전산화단층촬영으로 특이 진단이 불가능하였다. 6예 중 5 예(83.3%)에서 특이적 진단을 하였다. 전체 30예 중 단지 2예에서만 치료 방침의 결정적인 변화가 있었다. 결론: 미만성 간질성 폐질환 환자에서 고해상도 전산화단층촬영이 특이적 진단을 강력히 시사하는 경우에 개흉폐생검의 펼요성 여부에 대해서는 재검토가 필요할 것으로 생각된다.

• Journal of Chest Surgery
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• 제26권2호
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• pp.86-88
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• 1993

We have experienced 59 cases of videothoracoscopic operation for 7 months from January to August 1992 at Yongdong Severance Hospital, Yonsei University College of medicine. There were pneumothorax in 21 cases, mediastinal mass in 12 cases, diffuse intestitial lung disease in 7 cases, Buerger's disease in 1 case, metastatic lung cancer in 1 case and sclerosing hemangioma in 1 case. We had performed a variety of procedures (bullectomy in 21 cases, sympathectomy in 17 cases, mass excision in 12 cases, lung biopsy in 8 cases, lobectomy in 1 case). The patients were uneventful in post-operative courses.

• Safety and Health at Work
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• 제5권4호
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• pp.234-237
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• 2014

Background: Inhalation of asbestos fibers can lead to adverse health effects on the lungs. This study describes lung function profiles among individuals with nonmalignant asbestos-related disorders (ARDs). Methods: The study population was from the Workers' Compensation (Dust Diseases) Board of New South Wales, Sydney, Australia. Lung function measurements were conducted in males with asbestosis (n = 26), diffuse pleural thickening (DPT; n = 129), asbestosis and DPT (n = 14), pleural plaques only (n = 160) and also apparently healthy individuals with a history of asbestos exposure (n = 248). Standardized spirometric and single-breath diffusing capacity for carbon monoxide ($DL_{CO}$) measurements were used. Results: Mean age [standard deviation (SD)] was 66.7 (10.3) years for all participants. Current and ex-smokers among all participants comprised about 9.0% and 54.8%, respectively. Median pack-years (SD) of smoking for ex- and current-smokers were 22.7 (19.9). Overall 222 participants (38.6%) and 139 participants (24.2%) had forced expiratory volume in 1 second ($FEV_1$) and forced vital capacity (FVC) measurements < 80% predicted, and 217 participants (37.7%) had $FEV_1/FVC$ results < 70%. A total of 249 individuals (43.8%) had DLCO values < 80% predicted and only 75 (13.2%) had DLCO/VA results < 80% predicted. A total of 147 participants (25.6%) had peak expiratory flow (PEF) measurements < 80% predicted. The presence of ARDs lowered the lung function measurements compared to those of healthy individuals exposed to asbestos. Conclusion: Lung function measurement differs in individuals with different ARDs. Monitoring of lung function among asbestos-exposed populations is a simple means of facilitating earlier interventions.

• Tuberculosis and Respiratory Diseases
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• 제82권3호
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• pp.201-210
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• 2019

Background: Radial probe endobronchial ultrasound (R-EBUS) is widely used for diagnosing peripheral pulmonary lesions. However, the utility of R-EBUS-guided transbronchial lung biopsy (TBLB) for diffuse lung lesions (DLLs) remains unknown. We designed this study to evaluate the utility of R-EBUS-guided TBLB in DLLs. Methods: This retrospective study enrolled patients admitted from January 2016 to November 2017 who underwent TBLB for DLLs. The R-EBUS-guided TBLB and blind TBLB groups were compared. DLL was defined as any lung disorder that involved more than one segment of the lung. In both the groups, fluoroscopy and guided sheath were not used during TBLB. Results: A total of 127 patients underwent TBLB for DLLs (67 patients in the R-EBUS-guided TBLB group and 60 in the blind TBLB group). There were no differences in age, sex, and comorbid illnesses between the two groups. Furthermore, there was no difference in the TBLB diagnostic yield of the two groups (p=0.660) although more samples were collected from the R-EBUS-guided TBLB group (p=0.003). Procedure time was significantly longer in the R-EBUS-guided TBLB group than in the blind TBLB group (p<0.001). Thus, incidence of pneumothorax was significantly lower in the R-EBUS-guided TBLB group than in the blind TBLB group (p=0.032). Conclusion: Diagnostic yield in DLLs did not differ between the R-EBUS-guided TBLB and blind TBLB groups. Findings show that R-EBUS-guided TBLB in DLLs may reduce risk of pneumothorax.