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1.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-100691

RESUMO

Bronchobiliary fistula is a rare disorder consisting of an abnormal communication between the bronchial tree and the biliary duct. In Western countries, trauma, postoperative biliary stenosis, and biliary lithiasis are the predominant causative factors of bronchobiliary fistula. Bilioptysis (bile stained sputum) is a pathognomic finding for bronchobiliary fistula. To date, there are just a few reported cases of bronchobiliary fistula after sclerosis of a liver cyst. We describe the case of a 74-year-old woman who developed bronchobiliary fistula after sclerosing therapy of a liver cyst. The diagnosis was confirmed by the presence of bilioptysis and the chest and dynamic liver CT findings. The patient was successfully treated with antibiotics and percutaneous transhepatic catheter drainage.


Assuntos
Idoso , Feminino , Humanos , Antibacterianos , Catéteres , Constrição Patológica , Drenagem , Fístula , Litíase , Fígado , Soluções Esclerosantes , Esclerose , Tórax
2.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-129610

RESUMO

We report a case of Mycobacterium intracellulare pulmonary infection presenting as a solitary pulmonary nodule (SPN). A 35-year-old male was admitted due to a SPN in the right upper lobe which was detected on the chest radiography being examed due to recurrent cough for 1 year. The computed tomography (CT) revealed a spiculated nodule containing air-bronchogram, which was suspicious of malignancy. We performed transbronchial biopsy and the pathology showed granulomatous inflammation with caseous necrosis. Under the presumptive diagnosis of pulmonary tuberculosis, we started anti-tuberculous medication including isoniazid, rifampin, ethambutol, and pyrazinamide. In one month, however, the sputum culture was positive for Mycobacterium intracellulare. The follow-up chest CT showed slight aggravation of the previous lesions. Under the final diagnosis of Mycobacterium intracellulare pulmonary infection presenting as a solitary pulmonary nodule, we changed the regimen to rifampin, ethambutol, and clarithromycin. The follow-up chest CT after the completion of treatment, revealed resolution of the previous lesions.


Assuntos
Adulto , Humanos , Masculino , Biópsia , Claritromicina , Tosse , Etambutol , Seguimentos , Inflamação , Isoniazida , Pulmão , Pneumopatias , Complexo Mycobacterium avium , Infecções por Mycobacterium não Tuberculosas , Necrose , Pirazinamida , Rifampina , Nódulo Pulmonar Solitário , Escarro , Tórax , Tuberculose , Tuberculose Pulmonar
3.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-129595

RESUMO

We report a case of Mycobacterium intracellulare pulmonary infection presenting as a solitary pulmonary nodule (SPN). A 35-year-old male was admitted due to a SPN in the right upper lobe which was detected on the chest radiography being examed due to recurrent cough for 1 year. The computed tomography (CT) revealed a spiculated nodule containing air-bronchogram, which was suspicious of malignancy. We performed transbronchial biopsy and the pathology showed granulomatous inflammation with caseous necrosis. Under the presumptive diagnosis of pulmonary tuberculosis, we started anti-tuberculous medication including isoniazid, rifampin, ethambutol, and pyrazinamide. In one month, however, the sputum culture was positive for Mycobacterium intracellulare. The follow-up chest CT showed slight aggravation of the previous lesions. Under the final diagnosis of Mycobacterium intracellulare pulmonary infection presenting as a solitary pulmonary nodule, we changed the regimen to rifampin, ethambutol, and clarithromycin. The follow-up chest CT after the completion of treatment, revealed resolution of the previous lesions.


Assuntos
Adulto , Humanos , Masculino , Biópsia , Claritromicina , Tosse , Etambutol , Seguimentos , Inflamação , Isoniazida , Pulmão , Pneumopatias , Complexo Mycobacterium avium , Infecções por Mycobacterium não Tuberculosas , Necrose , Pirazinamida , Rifampina , Nódulo Pulmonar Solitário , Escarro , Tórax , Tuberculose , Tuberculose Pulmonar
4.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-28797

RESUMO

Among the bronchogenic carcinomas, especially squamous cell carcinoma and large cell carcinoma frequently present with cavitation, which may result from tumor necrosis. Cavitary lesions of the tumor are occasionally associated with infection and misdiagnosed as benign lung abscess owing to the partial responsiveness to antibiotics. It is very difficult to distinguish the carcinomatous abscess from the benign lung abscess, because of their similar clinical and radiologic features. Delay in diagnosis of underlying lung cancer may result in poor outcome. Therefore, clinicians should remember that the patients with highly suspicious carcinoma of the lung should undergo further precise examinations to find out malignant cells.


Assuntos
Humanos , Abscesso , Antibacterianos , Carcinoma Broncogênico , Carcinoma de Células Grandes , Carcinoma de Células Escamosas , Abscesso Hepático , Pulmão , Abscesso Pulmonar , Neoplasias Pulmonares , Necrose
5.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-13555

RESUMO

The middle mediastinum contains several important organs and pluripotent cells. It is difficult to make a definitive diagnosis in patients with middle mediastinal tumors due to a wide range of diseases. The likelihood of malignancy is influenced primarily by the following factors: patient age, size, tumor location, and the presence or absence of symptoms. We describe a case of a middle mediastinal tumor, which was suspected on chest x-ray; chest computed tomography revealed the eccentric mass of distal esophagus. This case emphasizes the diagnostic importance of the chest x-ray to the physicians. The possible differential diagnoses are reviewed.


Assuntos
Humanos , Diagnóstico Diferencial , Esôfago , Leiomioma , Neoplasias do Mediastino , Mediastino , Tórax
6.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-58890

RESUMO

Henoch-Schonlein purpura (HSP) is an immunologically mediated systemic vasculitis of small blood vessels that primarily involves the skin, gastrointestinal tract, joints and kidneys. HSP is a common vasculitic syndrome in children who, in most cases, achieve complete recovery. Pulmonary hemorrhage is a very rare manifestation of HSP. The authors present a case of a 46-year-old male presenting with pulmonary hemorrhage and renal involvement and the diagnosis of HSP. The patient responded to prednisolone therapy.


Assuntos
Criança , Humanos , Masculino , Pessoa de Meia-Idade , Vasos Sanguíneos , Trato Gastrointestinal , Hemorragia , Articulações , Rim , Prednisolona , Vasculite por IgA , Pele , Vasculite Sistêmica
7.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-101981

RESUMO

Lipoma is a common neoplasm in soft tissues. However, an intrapulmonary lipoma is a rare benign tumor. Patients with a bronchial lipoma might have a malignant potential related to their smoking history due to the case reports of lung cancer accompanied with lipoma. Endobronchial lipoma can cause irreversible parenchymal lung damage if not diagnosed and treated early. Therefore, it should initially be treated by fiberoptic bronchoscopy or surgery depending on the status of distal parenchymal lung damage. Bronchiolitis obliterans with organizing pneumonia (BOOP) is a pathological syndrome that is defined by the presence of buds of granulation tissue consisting of fibroblasts and collagen within the lumen of the distal air spaces. BOOP is caused by drug intoxication, connective tissue disease, infection, obstructive pneumonia, tumors, or an unknown etiology. We encountered a 58 year-old male patient with endobronchial lipoma, causing the collapse of the right middle and lower lobes, and BOOP due to obstructive pneumonia.


Assuntos
Humanos , Masculino , Bronquiolite , Bronquiolite Obliterante , Broncoscopia , Colágeno , Doenças do Tecido Conjuntivo , Pneumonia em Organização Criptogênica , Fibroblastos , Tecido de Granulação , Lipoma , Pulmão , Neoplasias Pulmonares , Pneumonia , Fumaça , Fumar
8.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-177318

RESUMO

A hiccup is caused by involuntary, intermittent, and spasmodic contractions of the diaphragm and intercostal muscles. It starts with a sudden inspiration and ends with an abrupt closure of the glottis. Even though a hiccup is thought to develop through the hiccup reflex arc, its exact pathophysiology is still unclear. The etiologies include gastrointestinal disorders, respiratory abnormalities, psychogenic factors, toxic-metabolic disorders, central nervous system dysfunctions and irritation of the vagus and phrenic nerves. Most benign hiccups can be controlled by traditional empirical therapy such as breath holding and swallowing water. However, though rare, a persistent hiccup longer than 48 hours can lead to significant adverse effects including malnutrition, dehydration, insomnia, electrolyte imbalance, and cardiac arrhythmia. An intractable hiccup can sometimes even cause death. We herein describe a patient with non-small cell lung cancer who was severely distressed by a persistent hiccup.


Assuntos
Humanos , Arritmias Cardíacas , Suspensão da Respiração , Carcinoma Pulmonar de Células não Pequenas , Sistema Nervoso Central , Clorpromazina , Contratos , Deglutição , Desidratação , Diafragma , Glote , Soluço , Músculos Intercostais , Neoplasias Pulmonares , Desnutrição , Nervo Frênico , Reflexo , Distúrbios do Início e da Manutenção do Sono , Água
9.
Yonsei Medical Journal ; : 69-77, 2007.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-200064

RESUMO

Human papillomavirus (HPV) infection is a co-carcinogen of lung cancer and contributes to its pathogenesis. To evaluate the prevalence of HPV infection, polymerase chain reaction (PCR) was employed to detect HPV 16, 18, and 33 DNA in tumor tissues of 112 patients with non-small cell lung cancer (NSCLC) who underwent curative surgery from Jan. 1995 to Dec. 1998 at Severance Hospital, Seoul, Korea. The patients consisted of 90 men and 22 women. Nineteen patients were under 50 years old (17%), and 92 patients (82%) were smokers. Fifty-three patients had adenocarcinomas, while 59 patients had non-adenocarcinomas. Early stage (I and II) cancer was found in 64 patients (57.1%) and advanced stage (III and IV) found in 48 (42.9%). The prevalence of HPV 16, 18, and 33 were 12 (10.7%), 11 (9.8%), and 37 (33.0%), respectively. Smoking status, sex, and histologic type were not statistically different in the presence of HPV DNA. The presence of HPV 16 was more common in younger patients and HPV 18 was more common in advanced stage patients. This study showed that the prevalence rate of HPV 16 and 18 infections in NSCLC tissue was low, suggesting HPV 16 and 18 infections played a limited role in lung carcinogenesis of Koreans. However, the higher prevalence of HPV 33 infections in Korean lung cancer patients compared to other Asian and Western countries may be important and warrants further investigation.

10.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-37546

RESUMO

BACKGROUND: For the diagnosis of pleural tuberculosis, polymerase chain reaction (PCR) of pleural effusion specimens has shown very low sensitivity, which might be due to the small number of bacilli in the samples. The purpose of this investigation is to determine whether the sensitivity of PCR testing can be improved when increasing the amount of pleural effusion specimens. METHODS: We prospectively analyzed pleural effusion specimens obtained from 53 patients for whom the exclusion of the possibility of tuberculous pleural effusion was necessary. We performed Mycobacterium tuberculosis PCR testing using the Cobas Amplicor MTB test (Roche Diagnostic Systems) with three different amounts (10ml, 25ml, and 50ml) of pleural effusion specimen in each patient. Pleural tuberculosis was defined as having one of the following: culture-positive pleural fluid sample, histopathologic finding consistent with tuberculosis on pleural biopsy, culture-positive sputum specimen, and/or positive response to anti-tuberculous medication without other possible causes of pleural effusion. RESULTS: Of the 53 patients, 26 received the diagnosis of pleural tuberculosis. The sensitivities of AFB smearing, Mycobacterium tuberculosis culture of pleural effusion specimen, pleural biopsy, and measurement of ADA were 3.8%, 15.4%, 84.6%, and 88.5%, respectively. The results of PCR testing were positive for 3 (11.5%), 4 (15.4%), and 3 (11.5%) of the 26 patients when using 10ml, 25ml, and 50ml of pleural effusion specimens, respectively. These results did not show a statistically significant difference in the sensitivity of PCR testing when increasing the amount of pleural effusion samples (p>0.05, symmetry exact test). CONCLUSION: For specimens such as pleural effusion, in which the bacillary load is very low, the clinical utility of PCR testing seems highly limited with the kits designed for the diagnosis of pulmonary tuberculosis. An increased amount of pleural effusion sample does not improve the sensitivity of PCR testing.


Assuntos
Humanos , Biópsia , Diagnóstico , Mycobacterium tuberculosis , Derrame Pleural , Reação em Cadeia da Polimerase , Estudos Prospectivos , Escarro , Tuberculose , Tuberculose Pleural , Tuberculose Pulmonar
11.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-160643

RESUMO

Antiphospholipid syndrome (APS) causes recurrent thromboses and morbidity during pregnancy, including fetal loss. This malady is associated with the persistent presence of anticardiolipin antibody or lupus anticoagulant. The pulmonary manifestations of antiphospholipid syndrome include pulmonary thromboembolism, pulmonary hypertension, acute respiratory distress syndrome, etc. Pulmonary thromboembolism is often the initial manifestation of antiphospholipid syndrome and a timely diagnosis is critical due to the high mortality rate. We herein report on a 19-year-old man with pulmonary thromboembolism that was caused by primary antiphospholipid syndrome. He presented with blood-tinged sputum, fever and epigastric pain, and his chest computerized tomography showed pulmonary thromboembolism. The other possible causes of pulmonary thromboembolism were excluded and the diagnosis of primary antiphospholipid syndrome was confirmed by the lupus anticoagulant that was present on two occasions six weeks apart. We also discuss the nature and management of antiphospholipid syndrome, along with a brief review of the relevant literatures.


Assuntos
Humanos , Gravidez , Adulto Jovem , Anticorpos Anticardiolipina , Síndrome Antifosfolipídica , Diagnóstico , Febre , Hipertensão Pulmonar , Inibidor de Coagulação do Lúpus , Mortalidade , Embolia Pulmonar , Síndrome do Desconforto Respiratório , Escarro , Tórax , Trombose
12.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-57204

RESUMO

Interferon alpha is an immunomodulator that is used as an antiviral agent to treat chronic active viral hepatitis C. However, interferon can induce or exacerbate sarcoidosis. We report a case of 42-year-old man with an exacerbation of pulmonary sarcoidosis after the cessation of interferon and ribavirin therapy for chronic hepatitis C. The patient's sarcoidosis improved spontaneously and he continues to be monitored regularly without steroid therapy.


Assuntos
Adulto , Humanos , Hepatite C , Hepatite C Crônica , Hepatite Crônica , Interferon-alfa , Interferons , Ribavirina , Sarcoidose , Sarcoidose Pulmonar
13.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-69158

RESUMO

BACKGROUND: Acute exacerbations form a major component of the socioeconomic burden of COPD. As yet, little information is available about the long-term outcome of patients who have been hospitalized with acute exacerbations, although high mortality rates have been reported. The aim of this study was to determine predictors of long-term mortality after hospitalization for acute exacerbation of COPD. METHODS: We performed a retrospective cohort study of consecutive patients admitted to the hospital for COPD exacerbation between 2000 through 2004. Patients who had died in hospital or within 6-months after discharge, had tuberculosis scar, pleural thickening or bronchiectasis by chest radiography or had been diagnosed with malignancy during follow-up periods were excluded. RESULTS: Mean age of patients was 69.5 years, mean follow-up duration was 49 months, and mean FEV1 was 1.00L (46% of predicted). Mortality was 35% (17/48). In the multivariate Cox regression analysis, heart rate of 100/min or more (p=0.003; relative risk [RR], 11.99; 95% confidence interval [CI], 2.34-61.44) and right ventricular systolic pressure (RVSP) of 35mmHg or more (p=0.019; RR, 6.85; 95% CI, 1.38-34.02) were independent predictors of mortality. CONCLUSION: Heart rate and RVSP in stable state may be useful in predicting long-term mortality for COPD patients admitted to hospital with acute exacerbation.


Assuntos
Humanos , Pressão Sanguínea , Bronquiectasia , Cicatriz , Estudos de Coortes , Seguimentos , Frequência Cardíaca , Hospitalização , Mortalidade , Doença Pulmonar Obstrutiva Crônica , Radiografia , Estudos Retrospectivos , Tórax , Tuberculose
14.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-195309

RESUMO

Hemangiopericytoma is a rare neoplasm that originates from small peri-capillary spindle shaped cells called pericytes. The most common sites of origin are the thigh, the pelvis and the retroperitoneum. A primary pulmonary hemangiopericytoma is particularly unusual. However, more than 50% of hemangiopericytoma cases metastasize to the lungs, the bone, and the liver. A long-term clinical and radiological follow up is recommended due to the high risk of recurrence of a potential malignancy. We report a case of a metastatic hemangiopericytoma in the lung that had initially developed in the thigh of a 53 year-old woman 6 years ago. The authors emphasize the long-term follow-up of this type of rare sarcoma.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Seguimentos , Hemangiopericitoma , Fígado , Pulmão , Metástase Neoplásica , Pelve , Pericitos , Recidiva , Sarcoma , Coxa da Perna
15.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-99077

RESUMO

BACKGROUND: IGFBP-3 inhibits the mitogenic and anti-apoptotic activity of IGF by blocking the binding of IGF to its receptor. However, under certain circumstances, IGFBP- 3 can enhance the activity of IGF by protecting IGF from its degradation. More than half of the inter- individual variations in IGFBP-3 levels are known to be genetically determined by the polymorphism at -202 locus of IGFBP-3 gene. METHOD: We attempted to ascertain whether A-202C poly?morphic variation of IGFBP-3 gene constitutes a risk factor for non-small cell lung cancer (NSCLC), using PCR-restriction fragment length polymorphism (RFLP). Our study included 104 NSCLC patients and 104 age-, gender-, and smoking status-matched control subjects. RESULT: In the 104 NSCLC subjects, the genotypic freque?ncies at the -202 site were as follows: AA = 67 (64.4%), AC = 35 (33.7%), and CC = 2 (1.9%). We did detect significant differences in the genotypic distribution between the NSCLC and the control subjects (pAC>CC). Using CC genotype as a reference, the odds ratio (OR) for the subjects with AC genotype was 2.60 (95% CI: 0.89 - 8.60), and the OR associated with AA genotype was 5.89 (95% CI: 1.92 - 21.16). CONCLUSION: These results indicate that the dysregulation of IGF axis should now be considered as another important risk factor for NSCLC, and a potential target for novel antineoplastic therapies and/or preventative strategies in high-risk groups.


Assuntos
Humanos , Vértebra Cervical Áxis , Carcinoma Pulmonar de Células não Pequenas , Genótipo , Proteína 3 de Ligação a Fator de Crescimento Semelhante à Insulina , Razão de Chances , Fatores de Risco , Fumaça , Fumar
16.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-25279

RESUMO

Serous effusions have been most commonly associated with ascites, pericardial effusion, and heart failure. But, they have been considered to be an unusual form of complication in hypothyroidism and pleural effusion, which has been observed as an isolated finding in hypothyroidism is apparently rare and complete analysis of these types of hypothyroid-associated pleural effusions has yet not been described. We report a case of hypothyroidism associated with unilateral pleural effusion in a 77 year-old male patient who was improved through levothyroxine sodium with brief review of the literature.


Assuntos
Idoso , Humanos , Masculino , Ascite , Insuficiência Cardíaca , Hipotireoidismo , Derrame Pericárdico , Derrame Pleural , Tiroxina
17.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-155447

RESUMO

Intraocular tumors are uncommon and an intraocular metastatic carcinoma is extremely rare. An intraocular metastasis in adults most often originates from the breast or the lung. An intraocular lesion may be the first presentation of cancer and a search should be made to locate the primary tumor. To our knowledge, an intraocular metastasis of a bronchioloaveolar carcinoma has not reported in Korea. We report a case of a bronchioloalveolar carcinoma presenting with the initial symptom of a unilateral visual disturbance due to an intraocular metastasis.


Assuntos
Adulto , Humanos , Adenocarcinoma Bronquioloalveolar , Mama , Coreia (Geográfico) , Pulmão , Metástase Neoplásica
19.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-191071

RESUMO

Bronchiolitis obliterans (BO) is a nonspecific inflammatory injury affecting primarily the small airways. Its inflammatory process is characterized by fibrotic obliteration of the lumen of bronchioles. BO can be idiopathic or associated with connective tissue disease, inhaled toxins, infections, drugs, and chronic graft-versus-host-disease (GVHD). Pulmonary complications occur in 40~60% of patients who undergo allogeneic bone marrow transplantation (BMT), causing 10~40% of transplant-related deaths. BO is a characteristic pulmonary complication which occurs usually within a few years after BMT. Documented complications of BO include air-leak syndromes such as pneumomediastinum, subcutaneous emphysema and pneumothorax. We report a case of a 30-year-old male patient with BO due to chronic GVHD after allogenic BMT who presented with recurrent bilateral pneumothoraces.


Assuntos
Adulto , Humanos , Masculino , Transplante de Medula Óssea , Medula Óssea , Bronquíolos , Bronquiolite Obliterante , Bronquiolite , Doenças do Tecido Conjuntivo , Doença Enxerto-Hospedeiro , Leucemia Mielogênica Crônica BCR-ABL Positiva , Enfisema Mediastínico , Pneumotórax , Enfisema Subcutâneo , Transplantes
20.
Artigo em Coreano | WPRIM (Pacífico Ocidental) | ID: wpr-95352

RESUMO

BACKGROUND: The purpose of this study was to evaluate the usefulness of the pleural fluid carcinoembryonic antigen (CEA) and cytokeratin fragment 19 (CYFRA 21-1) tumor markers as complementary tools for the diagnosis of malignant pleural effusions. PATIENTS AND METHODS: The levels of pleural and serum CEA and CYFRA 21-1 were prospectively assayed in 222 patients with pleural effusions (150 benign effusions, 57 bronchogenic carcinomas and 15 metastatic carcinomas). RESULTS: The levels of pleural fluid CEA and CYFRA 21-1 in the malignant effusions were significantly higher than those in the benign effusions. With a specificity of 95%, the cut off values for the CEA and CYFRA 21-1 in pleural effusions were 5 and 89 ng/ml, respectively. The diagnostic sensitivities of the pleural fluid CEA and CYFRA 21-1 in malignant effusions were 72 and 54%, respectively, whereas using a combination of the two, the sensitivity increased to 87% (p<0.05). CONCLUSIONS : These findings suggest that a combination of the pleural fluid CEA and CYFRA 21-1 in pleural effusions can be useful in the diagnosis of malignant pleural effusions.


Assuntos
Humanos , Antígeno Carcinoembrionário , Carcinoma Broncogênico , Diagnóstico , Queratinas , Derrame Pleural , Derrame Pleural Maligno , Estudos Prospectivos , Biomarcadores Tumorais
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