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1.
Tuberculosis and Respiratory Diseases ; : 219-223, 2008.
Artigo em Coreano | WPRIM | ID: wpr-77097

RESUMO

Pheochromocytoma is derived from the chromaffin tissue. The typical finding of pheochromocytoma is paroxysmal hypertension accompanied with various signs and symptoms that are due to the excess of catecholamines or other bioactive substances. Yet the diagnosis is sometimes difficult to make because its clinical presentation is quite variable. Especially, hemoptysis is a very rare symptom, so the diagnosis is often missed or delayed. Without making the correct diagnosis and then subsequently administering treatment, the condition may be fatal. We herein report on a 68 year-old woman who was admitted because of abdominal pain and hemoptysis. The initial radiologic findings suggested pulmonary edema with alveolar hemorrhage. The urine catecholamine levels were elevated and she developed catecholamine-induced cardiomyopathy. We performed bronchial arterial embolization and we administered alpha blocker medication for controlling the hemoptysis and hypertension. After the temporary symptomatic improvement, her clinical course was aggravated by pneumonia and pulmonary edema. In spite of performing definitive surgery for pheochromocytoma, she died of postoperative hemodynamic instability.


Assuntos
Feminino , Humanos , Dor Abdominal , Cardiomiopatias , Catecolaminas , Hemodinâmica , Hemoptise , Hemorragia , Hipertensão , Feocromocitoma , Pneumonia , Edema Pulmonar
2.
Tuberculosis and Respiratory Diseases ; : 480-485, 2007.
Artigo em Coreano | WPRIM | ID: wpr-72233

RESUMO

BACKGROUND: Chronic obstructive pulmonary disease (COPD) is characterized by airflow limitation that is not fully reversible. COPD has systemic effects, such as skeletal muscle dysfunction and abnormal weight loss. It also has been suggested that COPD is related to other chronic disease, such as cardiovascular disease, osteoporosis, and anemia. The aim of this study was to evaluate a symptom questionnaire and laboratory findings in subjects with air flow limitation. METHODS: We evaluated a symptom questionnaire and laboratory findings in subjects with airflow limitation detected by spirometry in conjunction with the Second Korean National Health and Nutrition Examination Survey. A total of 9,243 adults over the age of 18 were recruited. Among the adults, we finally analyzed 2,217 subjects who met the acceptability and repeatability criteria of spirometry, showed normal findings on chest radiography, and were older than 40 years of age. RESULTS: There were 288 subjects with airflow limitation as determined by spirometry. The frequency of respiratory symptoms such as cough, sputum and wheezing were significantly higher in subjects with airflow limitation (p<0.01). Hemoglobin and hematocrit levels were higher in subjects with airflow limitation (hemoglobin level 13.98 mg/dL vs. 13.62 mg/dL, hematocrit 42.10% vs. 40.89%; p<0.01). The HDL cholesterol level was lower in subjects with airflow limitation (44.95 mg/dL vs. 45.60 mg/dL; p<0.01). There was no significant difference in the total cholesterol, triglyceride, blood urea nitrogen, creatinine, and fasting glucose levels. CONCLUSION: In subjects with airflow limitation, prevalence of respiratory symptoms was higher than in normal spirometry subjects and the levels of hemoglobin and the hematocrit were higher. The HDL cholesterol level was lower in subjects with airflow limitation.


Assuntos
Adulto , Humanos , Anemia , Nitrogênio da Ureia Sanguínea , Doenças Cardiovasculares , Colesterol , HDL-Colesterol , Doença Crônica , Tosse , Creatinina , Jejum , Glucose , Hematócrito , Músculo Esquelético , Inquéritos Nutricionais , Osteoporose , Prevalência , Doença Pulmonar Obstrutiva Crônica , Inquéritos e Questionários , Radiografia , Sons Respiratórios , Espirometria , Escarro , Tórax , Triglicerídeos , Redução de Peso
3.
Journal of Lung Cancer ; : 47-50, 2006.
Artigo em Coreano | WPRIM | ID: wpr-98189

RESUMO

Lung cancer patients have increased risk of thromboembolism (TE) due to various factors such as by hypercoagulability, tumor thrombosis, decrease of ambulation, and chemotherapy etc. Among these factors, chemotherapy associated TEs have been reported, although the causes and pathomechanisms of TEs were not clear. Recently, reports proposed the potential role of platelets in endothelial damage by the chemotherapeutic agents. We have experienced a case of pulmonary TE after systemic chemotherapy with gemcitabine and cisplatin. The patient complained aggravated exertional dyspnea after chemotherapy and diagnosed as pulmonary TE by computerized tomogram. After anticoagulation and interruption of the chemotherapy, improvement of exertional dyspnea and resolution of the pulmonary TE were observed


Assuntos
Humanos , Cisplatino , Tratamento Farmacológico , Dispneia , Neoplasias Pulmonares , Pulmão , Embolia Pulmonar , Tromboembolia , Trombofilia , Trombose , Caminhada
4.
Tuberculosis and Respiratory Diseases ; : 248-255, 2006.
Artigo em Coreano | WPRIM | ID: wpr-57209

RESUMO

BACKGROUND: LOH11A is a region with frequent allele loss (>75%) in lung cancer that is located on the centromeric part of chromosome 11p15.5. Clinical and cell biological studies suggest that this region contains a gene associated with metastatic tumor spread. RRM1 encoding the M1 subunit of ribonucleotide reductase, which is an enzyme that catalyses the rate-limiting step in deoxyribonucleotide synthesis, is located in the LOH11A region. METHODS: Polymorphisms were found at nucleotide position (-)37 (C/A) and (-)524 (C/T) from the beginning of exon 1 of the RRM1 gene that might regulate the expression of RRM1. We studied the polymorphisms in 127 Korean individuals (66 lung cancer and 61 normal controls) and compared with those of 140 American patients with lung cancer. RESULTS: CC, AC and AA were found at the (-)37 position in 64(50.4%), 55(43.3%), and 8(6.3%) out of 127 Korean individuals (66 cancer, 61 non-cancer patients), respectively. There was a similar frequency of allele A at (-)37 in the American(27.9%) and Korean population(28.0%). CC, CT and TT was found at the (-)524 position in 24(18.9%), 44(34.6%), and 59(46.5%) out of the 127 Korean individuals, respectively. There was a similar frequency of allele C at (-)524 in the American(34.6%) and Korean population(36.2%).There was no difference in the frequency of the (-)37 and (-)524 genotypes between the cancer and non-cancer group. However there was a significant correlation of the genotypes between (-)37 and (-)524 (p<0.001), which suggests the possible coordination of these polymorphisms in the regulation of the promoter activity of the RRM1 gene. CONCLUSION: RRM1 promoter polymorphisms were not found to be significant risk factors for lung cancer. However, a further study of the promoter activity and expression of the RRM1 gene according to the pattern of the polymorphism will be needed.


Assuntos
Humanos , Alelos , Catálise , Éxons , Genes vif , Genótipo , Neoplasias Pulmonares , Pulmão , Ribonucleotídeo Redutases , Fatores de Risco
5.
Tuberculosis and Respiratory Diseases ; : 600-606, 2005.
Artigo em Coreano | WPRIM | ID: wpr-102880

RESUMO

BACKGROUND: The development of bronchoscopic equipment along with the precision of radiographic techniques had reduced the mortality rate of patients with tracheobronchial foreign bodies but has been no change in the incidence of tracheobronchial foreign bodies since their introduction. The aim of this study was to assess the clinical characteristics of a tracheobronchial foreign body aspiration and to evaluate the efficacy of the treatment modality in children and adults. METHODS: This is a retrospective review of 64 patients who underwent bronchoscopic procedures for the treatment of aspirated foreign bodies from December 1994 through March 2004 at the Chonnam national university hospital. RESULTS: There were 47 males and 17 females, aged from 1 month to 78 years. Most of the patients had no underlying illness except for one patient with a cerebrovascular accident that contributed to the foreign body aspiration. The most common symptom was cough, which was noted in 54 patients (84.3%). The other presenting symptoms were dyspnea (48.8%), fever (20.3%), sputum (14%), vomiting (7.8%), and chest pain (4.6%). Those whose tracheobronchial foreign bodies were diagnosed more than 2 days after the aspiration (21 patients) were more likely to have pneumonia than those whose foreign bodies were diagnosed within 2 days (p=0.009). Foreign bodies were visualized in the plain chest radiographs in 12 cases (18.8%), while others showed air trapping (21, 32.8%), pneumonia (15, 23.4%), atelectasis (7, 10.9%), and normal findings (9, 14.1%). The foreign bodies were more frequently found in the right bronchial tree (36) compared with the left bronchial tree (22, p=0.04). In order to remove the foreign bodies, twenty (31.2%) cases were removed using flexible bronchoscopy, while 42 (65.6%) and 2 (3.2%) cases required rigid bronchoscopy and surgery, respectively. CONCLUSIONS: Tracheobronchial Foreign body aspiration had a bimodal age distribution in the infancy and old age around 60 years. They were found more frequently in the right bronchial tree. In addition, patients whose foreign bodies were diagnosed more than 2 days after the aspiration were more likely have a infection. Rigid bronchoscopy is the procedure of choice for uncooperative children and for those with foreign bodies lodged deeply in the small bronchial tree.


Assuntos
Adulto , Criança , Feminino , Humanos , Masculino , Distribuição por Idade , Broncoscopia , Dor no Peito , Tosse , Dispneia , Febre , Corpos Estranhos , Incidência , Mortalidade , Pneumonia , Atelectasia Pulmonar , Radiografia Torácica , Estudos Retrospectivos , Escarro , Acidente Vascular Cerebral , Vômito
6.
Tuberculosis and Respiratory Diseases ; : 352-358, 2005.
Artigo em Coreano | WPRIM | ID: wpr-99078

RESUMO

Microsatellites are short tandem repeated nucleotide sequences that are present throughout the human genome. Variations in the repeat number or a loss of heterozygosity around the microsatellites have been termed a microsatellite alteration (MA). A MA reflects the genetic instability caused by an impairment in the DNA mismatch repair system and is suggested to be a novel tumorigenic mechanism. A number of studies have reported that MA in the DNA extracted from the plasma occurs at varying frequencies among patients with a non-small cell lung carcinoma (NSCLC). The genomic DNA from 9 subjects with a non-small cell lung cancer (squamous cell cancer 6, adenocarcinoma 2, non-small cell lung cancer1) and 9 age matched non-cancer control subjects (AMC: tuberculosis 3, other inflammatory lung disease 6) and 12 normal control subjects (NC) were extracted from the peripheral blood leukocytes and plasma. Three microsatellite loci were amplified with the primers targeting the Gene Bank sequence D21S1245, D3S1300, and D3S1234. MA in the form of an allelic loss or a band shift was examined with 6% polyacrylamide gel electrophoresis and silver staining. None (0/12) of the NC subjects less than 40 years of age showed a MA in any of the three markers, while 88.9%(8/9) of the AMC above 40 showed a MA in at least one of the three markers (p0.05). In conclusion, a MA in the D21S1245, D3S1300, and D3S1234 loci using DNA extracted from the plasma was detected in 66.7% of lung cancer while no MA was found in the young non-smoking control subjects. However, many of the non-cancer control subjects (aged smokers) also showed a MA, which compromised the specificity of the MA analysis as a screening test. Therefore, a further study with a larger sample size will be needed.


Assuntos
Humanos , Adenocarcinoma , Sequência de Bases , Carcinoma Pulmonar de Células não Pequenas , Reparo de Erro de Pareamento de DNA , DNA , Eletroforese em Gel de Poliacrilamida , Genoma Humano , Leucócitos , Perda de Heterozigosidade , Pneumopatias , Neoplasias Pulmonares , Pulmão , Programas de Rastreamento , Repetições de Microssatélites , Plasma , Tamanho da Amostra , Coloração pela Prata , Fumaça , Fumar , Tuberculose
7.
Journal of Korean Medical Science ; : 764-769, 2005.
Artigo em Inglês | WPRIM | ID: wpr-176550

RESUMO

To investigate whether hypercapnic acidosis, induced by adding CO2 to inspired gas, would be protective effect against ventilator-induced lung injury (VILI), we ventilated 55 normal white rabbits for 6 hr or until PaO2/FIO2 <200 mmHg. Control group (n=15) was ventilated with peak inspiratory pressure (PIP) of 15 cm H2O, positive end-expiratory pressure (PEEP) of 3 cm H2O, an inspiration-to-expiration ratio of 1:2, and an inspired oxygen fraction (FIO2) of 0.40. High pressure hypercapnic group (HPHC; n=20) was ventilated with PIP of 30 cm H2O, PEEP of 0 cm H2O, and FIO2 of 0.40. Carbon dioxide was introduced into the inspiratory limb of the ventilator circuit, as necessary to maintain hypercapnia (PaCO2, 65 to 75 mmHg). High pressure normocapnic group (HPNC; n=20) was ventilated with same setting of HPHC, except normocapnia (PaCO2, 35 to 45 mmHg). Bronchoalveolar lavage fluid (BALF) lactate dehydrogenase, aspartate aminotransferase, interleukin-8 were significantly higher in high pressure ventilator group than control group (p<0.05). Wet weight to dry weight (WW/DW) and histologic scores were significantly higher in high pressure ventilator group than control group (p<0.05). However, there were no significant differences in oxygenation, BALF inflammatory markers, WW/DW and histologic scores between HPHC and HPNC groups. These findings suggest that hypercapnic acidosis at least induced by CO2 insufflation would not be protective effect against VILI in this model.


Assuntos
Animais , Coelhos , Acidose Respiratória/induzido quimicamente , Administração por Inalação , Dióxido de Carbono/administração & dosagem , Hipercapnia/induzido quimicamente , Inalação , Troca Gasosa Pulmonar , Respiração Artificial/efeitos adversos , Síndrome do Desconforto Respiratório/diagnóstico , Resultado do Tratamento
8.
Journal of Lung Cancer ; : 128-132, 2004.
Artigo em Inglês | WPRIM | ID: wpr-65605

RESUMO

An endobronchial leiomyoma is extremely rare benign tumor of the lung. Most endobronchial leiomyomas reported in the literature have been resected by either a lobectomy or a pneumonectomy. Herein is report a case whose tumor was successfully removed using a fiberoptic bronchoscope without surgical resection. A 64-year-old female presented with a fever, and a cough with purulent sputum of 10 days duration. The bronchoscopy revealed a 1cm sized, glistening, light yellow colored mass lesion totally obstructing the orifice of the superior segment of the right lower lobe. During the bronchoscopic biopsy procedures, the mass lesion was completely removed. A diagnosis of a leiomyoma was made from a histological examination of the obtained specimen. The early diagnosis and appropriate treatment including bronchoscopic removal may prevent respiratory complications.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Biópsia , Broncoscópios , Broncoscopia , Tosse , Diagnóstico , Diagnóstico Precoce , Febre , Leiomioma , Pulmão , Pneumonectomia , Pneumonia , Escarro
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