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1.
Yonsei Medical Journal ; : 581-587, 2011.
Artigo em Inglês | WPRIM | ID: wpr-159917

RESUMO

PURPOSE: Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the airways and progressive destruction of lung parenchyma. Apoptosis is critical for the maintenance of normal tissue homeostasis and is in equilibrium with proliferation and differentiation. This study was undertaken to investigate relationship between apoptosis of peripheral blood lymphocytes during exacerbation of COPD and inflammatory response that characterizes this condition. MATERIALS AND METHODS: Seventeen patients with COPD exacerbation, 21 stable COPD, and 12 control subjects were included. T lymphocytes were isolated from peripheral blood using MACS. Apoptosis of T lymphocytes was assessed with FACS using annexin V and 7-aminoactinomycin. Serum levels of interleukin (IL)-6, IL-8 and tumor necrosis factor (TNF)-alpha were determined by an immunoassay technique. RESULTS: There was significantly increased percentage of apoptotic lymphocytes, CD 4+, and CD 8+ T cells in the peripheral blood of patients with exacerbation of COPD compared with stable COPD. Serum levels of IL-6, IL-8, and TNF-alpha were significantly increased in patients with exacerbation of COPD compared with stable COPD. Only TNF-alpha presented a positive correlation with apoptotic lymphocytes in patients with exacerbation of COPD. CONCLUSION: Increased apoptotic lymphocytes may be associated with upregulation of TNF-alpha in the peripheral blood of patients with acute exacerbation of COPD.


Assuntos
Humanos , Apoptose , Linfócitos T CD4-Positivos/patologia , Linfócitos T CD8-Positivos/patologia , Citometria de Fluxo , Interleucina-6/sangue , Interleucina-8/sangue , Doença Pulmonar Obstrutiva Crônica/sangue , Linfócitos T/patologia , Fator de Necrose Tumoral alfa/sangue
3.
Korean Journal of Medicine ; : 349-352, 2009.
Artigo em Coreano | WPRIM | ID: wpr-150704

RESUMO

A 54-year-old man presented with a cough, sputum, and fever. His chest X-ray showed atelectasis in the right middle lobe. Computed tomography revealed obstruction of the bronchus intermedius by an endobronchial tumor. The first bronchoscopic biopsy specimens suggested lipoma. We resected the tumor via rigid bronchoscopy under general anesthesia and the final pathology report revealed a cartilaginous hamartoma. Subsequently, he has been followed for more than 1 year without recurrence.


Assuntos
Humanos , Pessoa de Meia-Idade , Anestesia Geral , Biópsia , Brônquios , Broncoscopia , Tosse , Febre , Hamartoma , Lipoma , Atelectasia Pulmonar , Recidiva , Escarro , Tórax
4.
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
5.
Artigo em Coreano | WPRIM | ID: wpr-168141

RESUMO

Factitious hemoptysis is the bleeding type of Munchausen's syndrome, and this describes a group of patients who intentionally produce symptoms. Because factitious hemoptysis is a very rare manifestation of hemoptysis, it generally passes unnoticed. We report here on a case of factitious hemoptysis in a 15-year-old boy who presented with hemoptysis. During his three hospitalizations, we conducted many diagnostic procedures, including chest CT, laryngoscopy, bronchoscopy and bronchial arteriography, yet we failed to find the definitive cause of the patient's hemoptysis. He kept on complaining of repetitive hemoptysis and seizure-like activity. His father discovered that he had collected his blood into the specimen cup via an intravenous line. After we removed the intravenous line, he did not show blood to us again. We suggest that factitious hemoptysis should be considered in the differential diagnosis of hemoptysis of an unclear bleeding focus, and especially when the patient has a bizarre hospital course or unusual behavior. We also include a review of the relevant literature.


Assuntos
Adolescente , Humanos , Angiografia , Broncoscopia , Diagnóstico Diferencial , Pai , Hemoptise , Hemorragia , Hospitalização , Intenção , Laringoscopia , Tórax
6.
Artigo em Inglês | WPRIM | ID: wpr-182747

RESUMO

We experienced a rare case of sinonasal sarcoidosis initially presenting as nasal cavitary mass. When the clinical course was different from that of typical tuberculosis, physician should think the possibility of sarcoidosis, and re-biopsy or retrospective review of pathological findings might be helpful.


Assuntos
Cavidade Nasal , Estudos Retrospectivos , Sarcoidose , Tuberculose
7.
Artigo em Coreano | WPRIM | ID: wpr-223064

RESUMO

A sarcoidosis is a multisystemic granulomatous disorder that has a predilection for pulmonary involvement, and the common radiological findings for the disease are bilateral nodular or reticulonodular patterns. Pseudoalveolar sarcoidosis is a rare presentation of sarcoidosis. The radiological finding is an alveolar pattern that involves or compresses the alveoli by clustered interstitial granuloma. A 58-year-old man was admitted due to incidental findings of a unilateral consolidative lesion as seen on chest radiography. A chest computed tomography (CT) examination showed multiple bronchoalveolar consolidations that were suspicious of a malignancy. However, a percutaneous needle biopsy revealed non-caseating granuloma with an asteroid body that was compatible with sarcoidosis. After one month, the consolidative lesions improved without any treatment.


Assuntos
Humanos , Pessoa de Meia-Idade , Biópsia por Agulha , Granuloma , Achados Incidentais , Sarcoidose , Tórax
8.
Artigo em Coreano | WPRIM | ID: wpr-59554

RESUMO

Totally implanted central venous access devices for chemotherapy (chemoport) are being used increasingly in lung cancer patients. Vascular catheters are associated with various complications including infection, thrombosis as well as spontaneous fractures and embolization of the catheter, which is known as 'pinch-off syndrome'. 'Pinch-off syndrome' refers to the compression of a subclavian central venous catheter between the clavicle and first rib resulting in an intermittent or permanent obstruction, which can lead to tears, transection, or embolization. We report two cases of fractured and embolized implanted subclavian venous catheters in which the fragments were removed percutaneously. A 62-year-old man presented with back pain with a duration of a few weeks. The chest radiograph revealed complete transsection and embolization of the catheter into the right atrium. In addition, a 47-year-old woman with a chemoport had a grade 3 pinch-off sign in a chest radiograph demonstrating complete transsection and embolization of the catheter into the pulmonary artery. Both cases were managed by retrieving the embolized distal fragment percutaneously and removing the proximal section of the catheter.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Dor nas Costas , Catéteres , Cateteres Venosos Centrais , Clavícula , Tratamento Farmacológico , Fraturas Espontâneas , Átrios do Coração , Neoplasias Pulmonares , Pulmão , Artéria Pulmonar , Radiografia Torácica , Costelas , Trombose , Dispositivos de Acesso Vascular
9.
Artigo em Coreano | WPRIM | ID: wpr-59555

RESUMO

Recently, intra-Muscular Stimulation (IMS) therapy is being increasingly used for musculoskeletal pain. This procedure is generally regarded as a safe procedure for the general public. Some cases of iatrogenic pneumothorax caused by acupuncture have been reported in the medical literature. However, a case of an IMS therapy associated pneumothorax has not reported. We experienced two cases of iatrogenic pneumothorax after IMS therapy. A 62 year-old man received IMS therapy on the right shoulder due to posterior neck pain. After IMS therapy, acute dyspnea and chest discomfort developed. The other patient was a 74 year-old woman who also received IMS therapy. This patient experienced a nonproductive cough and acute dyspnea after the treatment. As the popularity of this form of alternative medicine increases, we might expect to see more cases of iatrogenic pneumothorax. Physicians should be aware of the adverse events associated with IMS therapy.


Assuntos
Idoso , Feminino , Humanos , Pessoa de Meia-Idade , Acupuntura , Terapias Complementares , Tosse , Dispneia , Dor Musculoesquelética , Cervicalgia , Pneumotórax , Ombro , Tórax
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