• Maxillofacial Plastic and Reconstructive Surgery
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• 제18권3호
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• pp.448-453
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• 1996

This is case report of florid osseous dysplasia occurred in the entire maxilla and mandible of 47-year-old female. Florid osseous dysplasia is an expansile, exuberant asymptomatic form of benign fibro-osseous disease of the periodontal ligament, often associated with jaw cysts and to be though as an abnormal reaction of bone to irritation or stimulation. The treatment was performed with removal of the necrotic bone, bone curretage and hyperbaric oxygen therapy. The patient did not well postoperatively and has shown sign of persistant infection with pus discharge.

• Journal of Chest Surgery
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• 제24권8호
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• pp.814-818
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• 1991

Infection with the ubiquitous fungus Aspergillus is uncommon. This organism has a low pathogenicity for man. In most patients, pulmonary Aspergilloma is the most common form of disease, and Aspergillus fumigatus is the common species. The natural history of the pulmonary aspergilloma is variable. This report reviews the feature of growing pulmonary aspergilloma for 10 years[from diameter 3cm to diameter 9cm]. This 44-year-old male patient suffered from recurrent hemoptysis for 10 years. This patient was taken removal of aspergilloma and cavernoplasty of left upper lobe. Post-operation course was uneventful.

• Investigative Magnetic Resonance Imaging
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• 제21권4호
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• pp.273-275
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• 2017

Thiemann's disease is a form of idiopathic avascular necrosis of the immature epiphyses of the phalanges of the fingers and toes. Few cases of Thiemann's disease have been reported because the disease is rare and difficult to diagnose. To the best of our knowledge, magnetic resonance imaging (MRI) findings of Thiemann's disease have not been reported. Here, we report a case of Thiemann's disease diagnosed by typical clinical symptoms and characteristic MRI findings before radiologic bony abnormalities were apparent.

• Imaging Science in Dentistry
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• 제43권4호
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• pp.295-301
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• 2013

The author experienced 8 cases of pericoronal radiolucency involving an incomplete tooth crown that had not developed to form the cemento-enamel junction, and the underdeveloped crown sometimes appeared to be floating within the radiolucency radiographically. The first impression was that these cystic lesions had odontogenic keratocysts, but half of them turned out to be dentigerous cysts histopathologically. There has been no report concerning odontogenic cysts involving an incompletely developed crown. The purpose of this paper is to report that dentigerous cysts may develop before the completion of the cemento-enamel junction of a developing crown.

• Journal of Chest Surgery
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• 제23권3호
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• pp.594-599
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• 1990

Congenital or acquired esophagotracheobronchial fistula are rare. The chief causes of the acquired form are malignancy developing on the esophagus or tracheobronchial system and infection, and trauma. The pathognomonic symptom is a paroxysmal cough occurring several seconds after ingestion of liquids. This report reviews a case of bronchoesophageal fistula of unknown origin accompanying bronchiectasis. The patient is 32 years old woman with excellent result by surgical intervention. But the fistula is accidently found in the operation field. The surgical procedures consissts of fistulectomy with Right lower lobectomy.

• Journal of Chest Surgery
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• 제56권1호
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• pp.49-52
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• 2023

A fistula from the right coronary artery draining into the left ventricle is a rare form of coronary artery fistula. Here, we describe the case of a symptomatic neonate with a large fistula of this type. The neonate was successfully treated with surgical closure of the fistula.

• 대한한의학회지
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• 제27권1호
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• pp.204-219
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• 2006

Objectives : This study is to report the proceeding of the project sponsored by the ministry of science and technology of Korea for the stroke study titled as 'fundamental study for standardization and objectification of differentiation and pattern identification of symptoms of Oriental Medicine in stroke'. Methods and Results : We works for clinical research and molecular epidemiology center and we are in charge of the development of case report form, education of the investigators, data entry, data validation, and analysis. In the process of this project, we need to development of standard operating procedures for development and education for the case report form. Conclusions : This study is to let researchers for Traditional Korean Medicine and clinical research know how to develop of case report form and standard operating procedures in clinical researches and maintain the resource document and data.

• 동의생리병리학회지
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• 제21권4호
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• pp.1051-1055
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• 2007

The diagnosis of pattern identification in Korean Medicine depend on Korean Medicine doctor's experience and information. So, Pattern identification in Korean Medicine raise a question of objectification. This study is to standard stroke pattern identification in Korean Medicine. Weight of symptoms was given important(1points), very important(2points) by stroke specialist. So weight of symptoms is used two method. One is total sum and the other is total man. One had been compared Pattern identification between diagnosed patients by medical specialists and by applicated weight in case report form. The other had been compared Pattern identification between intersubjectivity by medical specialists and by applicated weight in case report form. It is 38%(total sum) or 40%(total man) concordance rate between diagnosed patients by medical specialists and by applicated weight in case report form. It is 82.4% concordance rate between intersubjectivity by medical specialists and by applicated weight in case report form. To acquire more concrete data on this theme, we need further and large scale of prospective researches.

• 한국패류학회지
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• 제25권1호
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• pp.1-4
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• 2009

A specimen of the unknown form of Octopus species was collected from Onsan, Kyungsangnam-do, eastern coast of Korea on 20th June 2004 with a bottom trawl. The specimen distinguished from the other Octopus species reported hitherto by its extremely short 2nd pair of arm and hectocotilization of the right 4th arm. It may be described, therefore, as new species, but only one specimen was collected unfortunately. A new name will be deferred, consequently, until more specimens will be available in the future.

• Journal of Chest Surgery
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• 제32권10호
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• pp.966-969
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• 1999

Congenital defects of the sternum are rare development anomalies. They result form the failure of the lateral sternal bars to fuse. This malformation may be associated with other ventral midline fusion defects and ectopia cordis. A complete sternal cleft is the rarest form and less than 10 cases have been reported in the medical literature. Here were report a 3-day-old boy with complete sternal cleft without other malformations, who underwent primary surgical repair. Surgical correction of complete sternal cleft should be performed in neonatal period whether the infant if symptomatic or not because it is usually simple, able to achieve good result and primary repair is usually feasible at this period.