• Archives of Plastic Surgery
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• 제49권5호
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• pp.648-651
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• 2022

Nasal dermoid cysts are rare congenital anomalies that affect one in 20,000 to one in 40,000 individuals. Herein, we report a case of an initially misdiagnosed nasal dermoid cyst with intracranial extension. Among nasal dermoids, the lesion of the nasal tip is considered uncommon. Therefore, this should always be considered as a differential diagnosis of midline nasal masses, and a proper diagnostic approach should be taken.

• 대한두경부종양학회지
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• 제36권1호
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• pp.27-31
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• 2020

The midline nasal dermoid cysts are rare congenital neoplasms, which are diagnosed frequently in childhood. Masses are often noticeable at birth gaining size over time with recurrent infections and usually arise from the nasal cavity or lower 1/3 of the nasal dorsum. CT scan as the primary investigation is helpful to determine accurately the size and extent of the lesion as well as the integrity of adjacent bony structures. MRI scan is recommended to rule out an intracranial extension or sinus tracts. Treatment of choice is the complete surgical excision preserving the cyst wall. Here in, we present an unusual case of nasofrontal dermoid cyst in a 19-year-old boy without radiographic evidence of transcranial extension. In this case, we surgically removed nasofrontal dermoid cyst via transcolumellar approach. We also corrected saddle nose deformity after mass removal. Therefore, in this case, we experienced a successful case in which the nasofrontal dermoid cyst was totally removed without facial scar and deformity.

• Archives of Plastic Surgery
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• 제37권4호
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• pp.481-484
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• 2010

Purpose: Congenital dermoid cysts develop during the fusion of the embryo when the ectodermal tissue gets trapped in the line of fusion. Dermoid cysts of the head are rare lesions comprised of epidermal and mesodermal elements. Furthermore, dermoid cysts in the occipital area are extremely rare. Only a few cases of dermoid cysts in the posterior scalp have been reported. Especially, A bilateral, synchronous presentation in this location has not been reported previously in the literature. Methods: All 5 cases had a gradually enlarging mass of the posterior aspect of the scalp. The cysts were mobile, noncompressible, and non-tender, without evidence of an associated sinus tract, skin dimpling, discoloration, or communication with adjacent structures. The CT scan displayed a hypodense cystic lesions about -87 to +24 HU (Housefield units, average +3.2 HU) with hypodense capsule and no postcontrast enhancement. All tumors were found just under the skin, and were well encapsulated, so they were completely removed the mass with adjacent periosteum. Results: On gross findings, all tumors were oval-or round-shaped, and when the cystic tumor was cut open it presented a greasy and caseous substance. Histologically, all specimens contain desquamated squamous epithelium and keratin in the lumen and are encapsulated and lined by keratinized stratified squamous epithelium. And, all cases of posterior mass are the presence of adnexal structures. Conclusion: Appropriate diagnosis requires not only an index of suspicion for this rare tumor a very careful history and search for skin changes. Especially, CT can reveal the exact location of the cyst, its relationship with the adjacent structures. We think that occipital dermoids divide into superficial and deep type. In our cases, because they did not have intra-cranial involvement or fistula formation, they are superficial type. This report describes the clinical and operative aspects of the superficial dermoid cysts and provides a review of the literatures.

• Investigative Magnetic Resonance Imaging
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• 제21권2호
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• pp.114-118
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• 2017

Dermoid cysts are benign congenital tumors composed of keratinizing squamous epithelium and dermal derivatives. They account for less than 1% of all intracranial tumors and are rarely exhibited at the base of the skull. To the best of our knowledge, only one case report has presented computed tomography and conventional T1-weighted magnetic resonance (MR) findings that revealed an infratemporal dermoid cyst. In the present study, we report an unusual case of a dermoid cyst in the right infratemporal fossa, which was incidentally detected by MR imaging with the Dixon technique. This article also highlights the importance of meticulous radiological review and the usefulness of the Dixon technique in everyday clinical practice.

• Journal of Korean Neurosurgical Society
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• 제40권5호
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• pp.391-393
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• 2006

Dermoid cysts of the spinal canal are rare benign congenital tumors, accounting for $1{\sim}2%$ of all intraspinal tumors. We report a case of lumbar extramedullary cyst, combined with congenital sacral meningocele. The clinical features, characteristics on MRI, pathologic findings, and surgical treatment of such a rare extramedullary benign tumor is discussed with the relevant literature.

• 한국임상수의학회지
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• 제22권3호
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• pp.268-270
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• 2005

A corneal dermoid is a benign congenital mass usually affecting the lateral limbal region. A 3-month old male Shih Tzu dog with abnormal tissue on right cornea was referred to Veterinary Medical Teaching Hospital of Seoul National University. On ophthalmic examination, there was no evidence of visual impairment. Slit lamp biomicroscopy assessment revealed a mass, located in the inferior and temporal part of right cornea. The lesion was typically hemispheric and covered with pink skin. Superficial keratectomy was performed to remove the mass. On histopathological examination, the lesion was diagnosed as a corneal dermoid. Four months after operation, there had been no recurrence and hair regrowth.

• Advances in pediatric surgery
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• 제7권1호
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• pp.7-14
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• 2001

Congenital anomalies of the head and neck region such as preauricular sinus and skin tag, thyroglossal duct cyst, branchial anomaly, cystic hygroma and dermoid cyst are common in pediatric population. It is important for pediatricians and pediatric surgeons to be familiar with the embryology and the anatomical characteristic of these lesions in order to diagnose and treat them properly. Three hundred and nineteen patients with congenital head and neck anomalies treated at Hanyang University Hospital between 1980 and 1999 were reviewed to determine the relative frequency of the anomalies and to analyze the method of management. Eight-four (25.1 %) of 335 lesions were preauricular sinus and skin tag, 81 (24.2 %) were thyroglossal duct cyst, 81 (24.2 %) branchial anomaly, 58 (17.3 %) cystic hygroma and 31 were (9.2 %) dermoid cyst. The male-to-female ratio was 1.4:1. Thyroglossal duct cyst most commonly present at 3-5years, however branchial anomalies commonly are diagnosed in children younger than 1 year. Preauricular sinus showed familial tendency in three patients and was bilateral is 33.8 %. Most head and neck anomalies in children have specific clinical and anatomical characterics. A careful history and physical examination is very useful for diagnosis and proper management. Experienced pediatric surgeons should do the initial surgery since the recurrence rate after incomplete surgical excision can be high.

• 한국임상수의학회:학술대회논문집
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• 한국임상수의학회 2009년도 추계학술대회
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• pp.223-223
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• 2009

• Archives of Plastic Surgery
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• 제43권6호
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• pp.608-609
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• 2016

• Clinical and Experimental Pediatrics
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• 제49권9호
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• pp.1000-1004
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• 2006

Atretic encephalocele은 1972년 James와 Lassmann에 의해 meningocele manque로 처음 보고 되었고 뇌류의 퇴행성 형태로 정의하였다. 이후로 atretic, occult, abortive, rudimentary cephalocele 등의 다양한 명칭으로 명명되었으며 포함된 조직, 동반 기형, 발생 위치, 배아성 직정맥동의 유무 등에 따른 차이점들에 대해 다양하게 보고 되어왔다. 두정엽의 후부에 낭성 종물을 주소로 입원한 환아의 진단 과정에서 두부 초음파, CT, MRI를 시행하였으며 그 과정에서 MRI가 진단에 가장 효과적인 영상을 제공하였다. 환아 진단 후 수술적 방법으로 종물을 제거하였으며 수술 중 이상 소견 및 추후 관찰 기간 동안 이상 소견관찰되지 않았다. Atretic encephalcele의 희귀함과 진단 방법의 장단점 및 위치상 특성과는 다르게 동반 기형 및 발달 장애가 관찰되지 않은 증례를 치험 하였기에 보고하는 바이다.