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1.
Tuberculosis and Respiratory Diseases ; : 43-50, 2011.
Artigo em Coreano | WPRIM | ID: wpr-136343

RESUMO

BACKGROUND: Open lung biopsy is used for diagnosis of diffuse infiltrative lung diseases (DILD), but it is invasive and relatively expensive procedure. Fluoroscopy-guided cutting needle lung biopsy (FCNLB) has merits of avoidance of admission and rapid diagnosis. But diagnostic accuracy and safety were not well known in the diagnosis of DILD. METHODS: We included 52 patients (37 men, 15 women) having DILD on HRCT with dyspnea, except the patients who could be confidently diagnosed with clinical and HRCT findings. FCNLB was performed using 16G Ace cut needle (length 1.5 cm, diameter 2 mm) at the area of most active lesion on HRCT. Final diagnoses were made by the consensus. RESULTS: The mean interval between the HRCT and FCNLB was 4.5 days. Most cases were performed one biopsy during 5~10 minutes. Specific diagnosis was obtained in 43 of 52 biopsies (83%). The most common diagnosis was nonspecific interstitial pneumonia (11 cases) and followed by cryptogenic organizing pneumonia (7 cases), diffuse alveolar hemorrhage and usual interstitial pneumonia (5 cases in each), hypersensitivity pneumonitis (3 cases), tuberculosis and drug induced interstitial pneumonitis (2 cases in each), the others are in one respectively. Mild complication was developed in 9 patients (8 pneumothorax, 1 hemoptysis). Most of complications were regressed without treatment except one case with chest tube insertion for pneumothorax. CONCLUSION: Fluoroscopy-guided 16 G cutting needle lung biopsy was an useful method for the diagnosis of DILD.


Assuntos
Humanos , Masculino , Alveolite Alérgica Extrínseca , Biópsia , Biópsia por Agulha Fina , Tubos Torácicos , Pneumonia em Organização Criptogênica , Dispneia , Hemorragia , Fibrose Pulmonar Idiopática , Pulmão , Pneumopatias , Doenças Pulmonares Intersticiais , Agulhas , Pneumotórax , Tomografia Computadorizada por Raios X , Tuberculose
2.
Tuberculosis and Respiratory Diseases ; : 43-50, 2011.
Artigo em Coreano | WPRIM | ID: wpr-136342

RESUMO

BACKGROUND: Open lung biopsy is used for diagnosis of diffuse infiltrative lung diseases (DILD), but it is invasive and relatively expensive procedure. Fluoroscopy-guided cutting needle lung biopsy (FCNLB) has merits of avoidance of admission and rapid diagnosis. But diagnostic accuracy and safety were not well known in the diagnosis of DILD. METHODS: We included 52 patients (37 men, 15 women) having DILD on HRCT with dyspnea, except the patients who could be confidently diagnosed with clinical and HRCT findings. FCNLB was performed using 16G Ace cut needle (length 1.5 cm, diameter 2 mm) at the area of most active lesion on HRCT. Final diagnoses were made by the consensus. RESULTS: The mean interval between the HRCT and FCNLB was 4.5 days. Most cases were performed one biopsy during 5~10 minutes. Specific diagnosis was obtained in 43 of 52 biopsies (83%). The most common diagnosis was nonspecific interstitial pneumonia (11 cases) and followed by cryptogenic organizing pneumonia (7 cases), diffuse alveolar hemorrhage and usual interstitial pneumonia (5 cases in each), hypersensitivity pneumonitis (3 cases), tuberculosis and drug induced interstitial pneumonitis (2 cases in each), the others are in one respectively. Mild complication was developed in 9 patients (8 pneumothorax, 1 hemoptysis). Most of complications were regressed without treatment except one case with chest tube insertion for pneumothorax. CONCLUSION: Fluoroscopy-guided 16 G cutting needle lung biopsy was an useful method for the diagnosis of DILD.


Assuntos
Humanos , Masculino , Alveolite Alérgica Extrínseca , Biópsia , Biópsia por Agulha Fina , Tubos Torácicos , Pneumonia em Organização Criptogênica , Dispneia , Hemorragia , Fibrose Pulmonar Idiopática , Pulmão , Pneumopatias , Doenças Pulmonares Intersticiais , Agulhas , Pneumotórax , Tomografia Computadorizada por Raios X , Tuberculose
3.
Tuberculosis and Respiratory Diseases ; : 37-41, 2009.
Artigo em Coreano | WPRIM | ID: wpr-91426

RESUMO

Hot tub lung has been described as a pulmonary illness associated with exposure to nontuberculous mycobacteria, mainly hot bathtub water contaminated with Mycobacterium avium complex (MAC) and hence the name. Although not entirely clear, its etiology has been thought to involve either an infection or a hypersensitivity pneumonitis secondary to MAC. Herein, we describe 2 female patients (60 and 53 years old) admitted to our hospital with hot tub lung, and both of whom worked in a public bath. Both women were initially admitted following several months of exertional dyspnea and cough. The patients had been working as body-scrubbers in a public bath for several years. Their chest CT scans showed bilateral diffuse ground-glass opacities with multifocal air-trappings and poorly defined centrilobular nodules in both lungs. Pathological findings from lung specimens revealed small non-necrotizing granuloma in the lung parenchyme with relatively normal-looking adjacent alveoli. Discontinuation of working in the public bath led to an improvement in symptoms and radiographic abnormalities, without antimycobacterial therapy.


Assuntos
Feminino , Humanos , Alveolite Alérgica Extrínseca , Banhos , Tosse , Dispneia , Granuloma , Pulmão , Complexo Mycobacterium avium , Micobactérias não Tuberculosas , Tórax
4.
Tuberculosis and Respiratory Diseases ; : 416-420, 2008.
Artigo em Coreano | WPRIM | ID: wpr-168137

RESUMO

Many classes of drug, such as antineoplastic drugs and antiarrhythmic drugs, have potential to induce interstitial lung disease. Herbal medicines are also believed to have the potential to induce pneumonitis. However, to our knowledge, there are no reports of pneumonitis caused by herbal medications in the Korean medical database. We report a case of recurrent pneumonitis caused by a self rechallenge of the Herbal medicine Bojungikgitang (Bu-Zhong-Yi-Qi-Tang : Hochu-ekki-to).


Assuntos
Antiarrítmicos , Antineoplásicos , Medicina Herbária , Doenças Pulmonares Intersticiais , Pneumonia
5.
Journal of the Korean Society of Plastic and Reconstructive Surgeons ; : 103-105, 2008.
Artigo | WPRIM | ID: wpr-44943

RESUMO

PURPOSE: Fewer than 100 cases of calcifying aponeurotic fibroma have been reported in the literature since this entity was initially described by Keasbey in 1953 who called it calcifying juvenile aponeurotic fibroma. The tumor is a slowly growing, painless mass. In most cases the mass is poorly circumscribed and causes neither discomfort nor limitation of movement. Most lesions occur in children, with a peak incidence ages of 8-14 years. There is no evidence of any increased familial prevalence. Predilection sites are palm, finger, toe, but it also occurs in the wrist, forearm, elbow, upper arm, neck, abdominal wall, lumbar paravertebral area, leg and ankle. We herein describe a rare case of calcifying aponeurotic fibroma occurring on the chin with review of the literature. METHODS: A 14-year-old male had painless, slowly growing mass(phi2.5cm) on a chin for a year. The tumor was excised elliptically under local anesthesia and the excisional site was repaired directly. Due pathological examination was processed. RESULTS: Histological examination revealed an ill- defined fibrous growth that extends with multiple processes into the surrounding tissue with centrally located foci of calcification. The tumor is composed of short spindled plump fibroblasts with round or ovoid nuclei separated by collagenous stroma, showing vaguely palisading pattern. Diagnosis of calcifying aponeurotic fibroma was conferred. Postoperatively, the patient did well, and the lesion had not recurred. CONCLUSION: Fewer than 100 cases of calcifying aponeurotic fibroma have been reported in the literature. The most common occurring sites are palm, finger & toe, but it has been reported in the wrist, forearm, elbow, upper arm, neck, abdominal wall, lumbar paravertebral area, leg and ankle. Two cases of calcifying aponeurotic fibroma occurring on the neck have been reported in the literature. To the authors knowledge, our case of calcifying aponeurotic fibroma occurring on the chin is the first to be reported.


Assuntos
Adolescente , Animais , Criança , Humanos , Masculino , Parede Abdominal , Anestesia Local , Tornozelo , Braço , Queixo , Colágeno , Cotovelo , Fibroblastos , Fibroma , Dedos , Antebraço , Incidência , Perna (Membro) , Pescoço , Prevalência , Dedos do Pé , Punho
6.
Korean Journal of Dermatology ; : 858-860, 2006.
Artigo em Coreano | WPRIM | ID: wpr-24220

RESUMO

Clear cell acanthoma is a rare, benign tumor of epidermal origin, with distinct histolopathological features which usually includes solitary or rarely multiple tumors, often localized on the lower legs of middle-aged or elderly people. It presents as a flat or dome-shaped, sharply-demarcated papule or nodule, sometimes with a keratotic scale of bright red or pink color. Histopathological findings include clear cells within sharply-demarcated area of the epidermis. We report a case of clear cell acanthoma which developed on the lateral side of the right foot of an 82-year-old man.


Assuntos
Idoso , Idoso de 80 Anos ou mais , Humanos , Acantoma , Epiderme , , Perna (Membro)
7.
Yonsei Medical Journal ; : 140-143, 2006.
Artigo em Inglês | WPRIM | ID: wpr-69171

RESUMO

Inflammatory pseudotumor (IPT) of the liver is rare benign tumor. When the diagnosis of IPT is established with biopsy, simple observation or conservative therapy is preferred because of the possibility of regression. But IPT is unresponsive to the conservative treatment, surgical resection should be considered. We experienced a 63-year-old male, who was suspected hepatocellular carcinoma in abdominal computed tomography (CT) and magnetic resonance image (MRI) scan, presented with 2-month history of intermittent fever and weight loss. Percutaneous ultrasound guided core biopsy confirmed IPT of the liver. Non-steroidal anti-inflammatory drugs and antibiotics were administered for 8 and 4 weeks, respectively, but fever continued. So, extended right hepatectomy was performed for IPT of the liver and then fever subsided. The patient remains well during a follow-up period of 12 months.


Assuntos
Pessoa de Meia-Idade , Masculino , Humanos , Imageamento por Ressonância Magnética , Hepatopatias/diagnóstico , Fígado/patologia , Hepatectomia , Granuloma de Células Plasmáticas/diagnóstico , Diagnóstico Diferencial
8.
Korean Journal of Urology ; : 197-199, 2005.
Artigo em Coreano | WPRIM | ID: wpr-79029

RESUMO

Metastatic cancers in the spermatic cord are extremely rare. A 79-year-old man, who had undergone palliative chemotherapy and radiotherapy one year previously, due to inoperable esophageal cancer, visited our hospital suffering from right inguinal swelling. Ultrasonography showed echogenic lesions superior to the right testis, suspicious of a swollen bowel loop. An emergency exploration revealed no bowel content or mesentery, but with thickened of the spermatic cord and epididymis four times that of the contralateral side. Pathology confirmed a metastatic carcinoma, likely to have originated from the esophagus.


Assuntos
Idoso , Humanos , Masculino , Tratamento Farmacológico , Emergências , Epididimo , Neoplasias Esofágicas , Esôfago , Hérnia , Mesentério , Metástase Neoplásica , Patologia , Radioterapia , Cordão Espermático , Testículo , Ultrassonografia
9.
Korean Journal of Gastrointestinal Endoscopy ; : 90-93, 2003.
Artigo em Coreano | WPRIM | ID: wpr-15387

RESUMO

Neurofibromatosis type 1, an autosomal dominant disorder, is clinically characterized by the presence of cafe-au-lait spots and cutaneous neurofibromas. Malignancy is a frequently cited and feared complication of neurofibromatosis. Neurofibromatosis has been reported to be associated with some CNS tumors, neurofibrosarcoma, pheochromocytoma, and nonlymphocytic leukemia. Also malignant lymphoma may develop in patients with neurofibromatosis. In Korea, only a case of lung cancer and a case of pheochromocytoma have been reported to develop in patients with neurofibromatosis type 1. Recently, we experienced a case of malignant lymphoma involving the stomach in a 70-year-old woman with neurofibromatosis type 1. An esophagogastroduodenoscopy revealed a 5 cm sized ulcerofungating mass on the greater curvature of the upper body. Histologic diagnosis of the biopsied specimen was B-cell diffuse small and large cell lymphoma. This case illustrates that malignant lymphoma should be included in the differential diagnosis of gastric tumors in patients with neurofibromatosis type 1.


Assuntos
Idoso , Feminino , Humanos , Linfócitos B , Manchas Café com Leite , Diagnóstico , Diagnóstico Diferencial , Endoscopia do Sistema Digestório , Coreia (Geográfico) , Leucemia , Neoplasias Pulmonares , Linfoma , Linfoma de Células B , Neurofibroma , Neurofibromatoses , Neurofibromatose 1 , Neurofibrossarcoma , Feocromocitoma , Estômago
10.
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 1196-1198, 2002.
Artigo em Coreano | WPRIM | ID: wpr-649260

RESUMO

Granular cell tumor is a rare, usually benign neoplasm that can occur in various parts of the body. Half of all granular cell tumors occur in the head and neck, with 33% of these occurring in the tongue. The larynx is relatively an uncommon location, accounting for approximately 7% to 10% of all reported cases. Typically, the most common presenting symptom is hoarseness, with some patients also presenting stridor, hemoptysis, dysphagia, and otalgia. But the tumor may be asymptomatic and discovered only incidentally during a routine examination. The diagnosis is usually made on the histopathological findings, characterized by abundant eosinophilic cytoplasm filled with granules of varying sizes. Complete excision with an attempt to maintain normal structures generally results in cure. We experienced a 16-year-old man with laryngeal granular cell tumor, which involves the right true vocal fold. He was successfully treated with local excision under laryngomicroscopic fine dissection. So we present this case with a review of literature.


Assuntos
Adolescente , Humanos , Citoplasma , Transtornos de Deglutição , Diagnóstico , Dor de Orelha , Eosinófilos , Tumor de Células Granulares , Cabeça , Hemoptise , Rouquidão , Neoplasias Laríngeas , Laringe , Pescoço , Sons Respiratórios , Língua , Prega Vocal
11.
Journal of the Korean Society for Microbiology ; : 203-214, 2000.
Artigo em Coreano | WPRIM | ID: wpr-216454

RESUMO

Porphyromonas gingivalis has been implicated in periodontal diseases. Accumulating evidence suggests that cardiovascular disease is the most prevalent medical problem in patients with periodontal diseases. In order to check the possibility that P. gingivalis is involved in coronary heart disease, the present study was performed to observe P. gingivalis adherence and invasion of human coronary artery endothelial cells (HCAEC) and production of cytokines and growth factors by HCAEC upon P. gingivalis infection. 3H-labeled P. gingivalis 381 was incubated with HCAEC for 90 min. The radioactivity of the washed HCAEC was a measure of the absorbed (adhering and invading) P. gingivalis. The absorption radioactivity of the HCAEC infected by P. gingivalis was determined to be 59.58% of the input bacterial cells. In contrast, the absorption radioactivity of the cells infected by S. gordonii Challis which was employed as a control was negligible (0.59%). DPG3, a P. gingivalis mutant defective of fimbriae, appeared to be impaired to some extent in capability of adherence/invasion as compared to that of the parental strain 381, showing 43.04% of the absorption radioactivity. The absorption radioactivity of the HCAEC infected by P. gingivalis 381 in the presence of excessive fimbriae at the concentrations of 50 mug and 100 mug/ml was 57.27 and 45.44%, respectively. Invasion of HCAEC by P. gingivalis 381 was observed by an antibiotic (metronidazole) protection assay and transmission electron microscopy (TEM). In the antibiotic protection assay, invasion by the bacterium was measured to be 0.73, 1.09, and 1.51% of the input bacterial cells after incubation for 30, 60, and 90 min, respectively. Invasion by DPG3 was shown to be 0.16% after 90-min incubation. In comparison of invasion efficiency at 90 min of the incubation, the invasion efficiency of DPG3 was 0.37% while that of its parental strain 381 was 2.54%. The immunoblot analysis revealed fimbriae of P. gingivalis did not interact with the surface of HCAEC. These results suggest that fimbriae are not the major contribution to the adherence of P. gingivalis to HCAEC but may be important in the invasion of HCAEC by the bacterium. The presence of cytochalasin D (1 mug/ml) and staurosporine (1 muM) reduced the invasion of HCAEC by P. gingivalis 381 by 78.86 and 53.76%, respectively, indicating that cytoskeletal rearrangement and protein kinase of HCAEC are essential for the invasion. Infection of P. gingivalis induced HCAEC to increase the production of TNF-alpha by 60.6%. At 90 min of the incubation, the HCAEC infected with P. gingivalis cells was apparently atypical in the shape, showing loss of the nuclear membrane and subcellular organelles. The overall results suggest that P. gingivalis may cause coronary heart disease by adhering to and invading endothelial cells, and subsequently damaging the cells.


Assuntos
Humanos , Absorção , Doenças Cardiovasculares , Doença das Coronárias , Vasos Coronários , Citocalasina D , Citocinas , Células Endoteliais , Peptídeos e Proteínas de Sinalização Intercelular , Microscopia Eletrônica de Transmissão , Membrana Nuclear , Organelas , Pais , Doenças Periodontais , Porphyromonas gingivalis , Porphyromonas , Proteínas Quinases , Radioatividade , Estaurosporina , Fator de Necrose Tumoral alfa
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