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자료유형
학술저널
저자정보
Shin, Nan-Young (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Kang, Ju Hee (Department of Oral and Maxillofacial Radiology, Seoul National University Dental Hospital) Kim, Jo-Eun (Department of Oral and Maxillofacial Radiology, Seoul National University Dental Hospital) Symkhampa, Khantaly (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Huh, Kyung-Hoe (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Yi, Won-Jin (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Heo, Min-Suk (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Lee, Sam-Sun (Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University) Choi, Soon-Chul (Department of Oral and Maxillofacial Radiology and Den)
저널정보
대한영상치의학회 Imaging science in dentistry Imaging science in dentistry 제49권 제4호
발행연도
2019.1
수록면
317 - 321 (5page)

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Steatocystoma multiplex is an uncommon benign skin disease, which typically manifests as numerous intradermal cysts that can be scattered anywhere on the body. Although usually asymptomatic, it can be significantly disfiguring. One type of steatocystoma multiplex is known to be associated with the autosomal dominant inheritance of a mutation in the gene coding for keratin 17 (KRT17). In such cases, it is often concurrent with other developmental abnormalities of the ectoderm-derived tissues, such as the nails, hair, and teeth. To the best of our knowledge, few cases have been reported of steatocystoma multiplex of the oral and maxillofacial region. This report describes a case of steatocystoma multiplex of both sides of the neck and multiple dental anomalies, with a focus on its clinical, radiological, and histopathological characteristics, as well as the possibility that the patient exhibited the familial type of this condition.

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