• 대한치과의사협회지
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• 제23권10호통권197호
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• pp.827-827
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• 1985

• 대한치과의사협회지
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• 제23권11호통권198호
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• pp.917-917
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• 1985

• 대한치과의사협회지
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• 제22권1호통권176호
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• pp.6-6
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• 1984

• 한국동물학회:학술대회논문집
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• 한국동물학회 2000년도 한국생물과학협회 학술발표대회
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• pp.201.1-201
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• 2000

• 대한핵의학회:학술대회논문집
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• 대한핵의학회 1972년도 제11차 학술대회
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• pp.66.2-66.2
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• 1972

• Journal of Korean Neurosurgical Society
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• 제40권1호
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• pp.47-50
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• 2006

This 51-year-old man suffered from paraparesis of 1-week history. On preoperative images, spinal cord compression by infiltrative vertebral mass was shown at T3 and T4 level. Several months earlier, he underwent surgical resection of left 2nd to 4th ribs, due to painful growing chest wall mass, which was proved to be hepatocellular carcinoma. All available diagnostic procedure failed to uncover origin of malignancy. Operation was followed by adjuvant irradiation and chemotherapy to the vertebral mass, however he only to die in 3 months after operation. This is an extremely rare case of ectopic hepatocellular carcinoma at thoracic vertebrae which showed very aggressive clinical course. Possible pathogenic process is presented and discussed.

• Journal of Korean Neurosurgical Society
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• 제52권2호
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• pp.152-155
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• 2012

A Rathke's cleft cyst (RCC) is a benign pituitary cyst derived from the remnant of Rathke's pouch, and usually presents as an intrasellar lesion with varying degrees of suprasellar extension. However, to date, a description of a primary prepontine RCC with no intrasellar component has not been reported. The author describes an exceptional case of a symptomatic RCC located behind the sella turcica in a 41-year-old woman who presented with severe headache. The author also provides an embryological hypothesis of the development of an ectopic RCC, with a special emphasis on radiologic characteristics.

• 대한기관식도과학회지
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• 제16권1호
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• pp.64-67
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• 2010

Congenital esophageal stenosis due to tracheobronchial remnants is a rare anomaly, resulting in dysphagia and recurrent pneumonia, We have experienced three cases of csophageal stenosis due to ectopic tracheobronchial remnants and performed operative correction. Two patients were 20 months and five year old male with a chief complaints of swallowing difficulty from birth and the other was a twenty three year old female with a slowly increasing symptom of dysphagia for twenty years. Esophagogram of the patient with tracheobronchial remnants shows abrupt narrow segment at distal esophagus with marked proximal dilatation, and linear barium collections perpendicularly projecting from the stenotic esophagus. All of them were performed surgical correction by esophagectomy of the stenotic portion and esopahgo-gastrostomy with anti-reflux procedures, The resected specimens of these patients showed ectopic tracheobronchial chondroepithelial tissue within the esophageal wall histopathologically. Postoperative course was uneventful and have been in good condition without any problems.

• 대한치과의사협회지
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• 제25권11호통권222호
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• pp.1069-1077
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• 1987

Two brothers aged 15 1/6 and 12 2/3 years were diagnosed as Class I malocclusion with ectopic eruption of the upper left central incisor in the elder brother and etopic eruption in the upper right second premolar in the younger. All 4 second molars were extracted at the same time in both brothers. The treatment results were as follows. 1. In the elder brother, the third molars were fully erupted and their angulations were excellent at 3 years post-treatment. 2. In the younger brother, the lower right third molar was mesially erupted and upper third molars were still undergoing eruption at 3 years post-treatment. 3. Assessment of panex films of both brothers at aged 15 showed an earlier eruption of the third molars in the younger brother. 4. A longer post-treatment supervision of the third molars was required in the younger brother. 5. The facial probiles were enhanced and the ectopic eruptions were corrected in both brothers.

• Imaging Science in Dentistry
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• 제38권2호
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• pp.109-115
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• 2008

The basal cell nevus syndrome (BCNS) is an autosomal dominant disorder, characterized by basal cell carcinomas, odontogenic keratocysts and skeletal abnormalities. We experienced two cases that represented several characteristics of BCNS. Case 1: a thirty three year-old man visited CSU hospital. His radiographs showed four cystic lesions at both maxillary sinus and both mandibular angle, with bifid rib and ectopic calcification of falx cerebri. After marsupialization and enucleation, recurrent and newly developing tendency were found on his follow-up radiographs. Case 2: a seventeen year-old man had four large cystic lesions which were diagnosed as odontogenic keratocysts. He had craniofacial anomalies which included ectopic calcification and frontal bossing.