KMID : 1024020190490040317
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Imaging Science in Dentistry 2019 Volume.49 No. 4 p.317 ~ p.321
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Steatocystoma multiplex: A case report of a rare entity
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Shin Nan-Young
Kang Ju-Hee Kim Jo-Eun Symkhampa Khantaly Huh Kyung-Hoe Yi Won-Jin Heo Min-Suk Lee Sam-Sun Choi Soon-Chul
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Abstract
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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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KEYWORD
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Steatocystoma Multiplex, Computed Tomography, Keratin-17
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