• 대한두개안면성형외과학회지
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• 제23권5호
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• pp.241-245
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• 2022

Cervical chondrocutaneous branchial remnants are very rare congenital lesions of the lateral neck; thus, our knowledge of this condition derives almost entirely from occasional case reports in the literature. They are thought to originate from the branchial arches and, therefore, can be found anywhere on the pathway along which those branchial arches migrate during embryogenesis. We report the case of a 5-year-old girl presenting with a cervical chondrocutaneous branchial remnant on the right lateral neck that had existed since birth, with no other anomalies.

• 대한두경부종양학회지
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• 제25권1호
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• pp.12-17
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• 2009

Background and Objectives : Branchial anomaly is a common neck pathology seen by otolaryngologist. Although there is still controversy regarding the origin, almost all surgeon agree that branchial anomalies result from incomplete involution of the branchial apparatus. Depending on its anatomic location, branchial anomalies can be classified into first, second, third and fourth anomaly. The purpose of this study is to evaluate the incidence of different categories of branchial anomalies and to determine proper method of diagnosis and treatment. Subjects and Method : A retrospective chart review was conducted for 72 patients with branchial anomalies operated on at the Korea University Anam Hospital from 1996 to 2007. The patient's sex, age, presenting symptoms, classification, site of lesion, diagnostic studies, surgical therapy and post-operative surgical complication were reviewed. Results : Patients were commonly seen in the 3rd decades. Eleven patients(15.3%) were first branchial anomalies, 52(72.2%) were second, 1(1.4%) was third, and 8(11.1%) were fourth. Of the types of anomalies, cyst were most commonly seen. In cases of 3rd and 4th branchial anomalies, barium contrast study can delineate the course of sinus or fistula. All cases was operated on for branchial anomalies, there were no major post-operative complication. Conclusion : Cervical mass and recurrent cervical infection or abscess are suspect for branchial anomalies. Especially, clinical history of dysphagia, and recurrent painful swelling in the thyroid region in young patients should raise the suspicion of 3rd and 4th branchial anomalies. Careful history, clinical examination and radiographic study were essential parts in diagnosis of branchial anomalies. Although surgical management of branchial anomalies depend on its type, nature and extent, complete excision is the major surgical procedure.

• 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.

• 대한기관식도과학회:학술대회논문집
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• 대한기관식도과학회 1972년도 춘계종합 학술대회 초록집
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• pp.16.2-16
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• 1972

선천성 경부의 종은 태생기발육 이상에 의한 유잔물에 기인하는 것으로 비교적 드물게 보는 질환이다. 최근 저자들은 측경부에 점차 증대하는 종류를 주소로하여 내원한 3예와 갑상선상부에 발생한 종류를 주소로 하여 내원한 4예를 경험하였다. 이들 환자들에 대한 임상증상, 이학적 소견, X-선검사 및 갑상선기능검사등에 의하여 측경부에 발생한 종류는 갑상선설관낭종이란 진단하에 외과적 유출을 시행하였으며 병리조직학적으로 확진되었기에 보고하는 바이다.

• 대한두경부종양학회지
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• 제26권1호
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• pp.45-47
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• 2010

Accessory tragus is an uncommon congenital anomaly of the external ear. The tragus derives from the first branchial arch. The accessory tragus can be found along the entire course of embryonic migration. Usually it appears as a small papules arising near the tragus, but rarely, along an imaginary line drawn back from the tragus to the angle of the mouth, or along the anterior edge of the sternocleidomastoid muscle and the sternoclavicular region. We experienced a case of accessory tragi on the suprasternal region in an 9 year-old-boy.

• 대한두경부종양학회지
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• 제14권2호
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• pp.260-262
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• 1998

Metastatic squamous carcinoma of the head and neck may rarely present as a cyst in the cervical region. The true incidence of metastatic cystic neck mass is unknown. It is difficult to differentiate metastatic cystic neck mass from congenital cystic neck mass with physical examination and fine needle aspiration biopsy. So the differential diagnosis is dependent on the age of the patient, and therefore in the patient over the 40 years of age, the possibility of a metastatic neck mass should be considered. We report a metastatic cystic neck mass which had been misdiagnosed as a branchial cleft cyst.

• 대한두개안면성형외과학회지
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• 제18권4호
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• pp.287-291
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• 2017

Preauricular sinus is a congenital malformation that is very commonly encountered among the general population and it has especially high prevalence among Asians when compared to other ethnic groups. It can often go unnoticed or easily overlooked by the patient or even by doctors because most of them are asymptomatic and is most of the time only a tiny pit that can be trivial in terms of aesthetics. We report a very rare and unique case that has no precedence what so ever; hence no reported case in the literature: an ectopic preauricular sinus in a facial cleft and microsomia patient.

• 한국어병학회지
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• 제29권1호
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• pp.1-5
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• 2016

Isopods are parasitic crustaceans that pose serious threat to fisheries. Several studies have tried to explore the host-pathogen relationship between marine fishes and isopods. The present study aims to understanding the secondary infections in marine fishes pertaining to isopods. To assess the secondary infection in infected fishes, parasite infested and healthy tissues of fishes were collected. The samples were subjected to standard microbiological procedure to identify the presence of pathogenic bacteria and fungi. Our results showed the branchial region had the higher microbial load of non-sporulating cenocytic fungi in infected fishes. Moreover, fungal strains isolated from the parasitic lesion confirmed that the parasitation and body lesion facilitates the entry of several pathogenic microbes at the damaged host tissue. More over the immune regulation of fish fights back by producing minute cysts, trying to encapsulate the growing fungus. But this may eventually lead to systemic infestation and death of the fish.

• Journal of Chest Surgery
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• 제29권9호
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• pp.1023-1027
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• 1996

경동맥체 종양(carotid body tumor)은 총경동맥 분지부에 위치한 경동맥체 즉 화학 수용기에서 발생하는 종양으로서 그 발생빈도가 드물다. 이 경동맥 체의 기능은 혈액내 화학조성에 의해 호흡,혈압, 맥박수의 반사조절이 이루어지는 것으로 알려져 있다. 조직학적으로 대부분 주세포(chiefcell)로 구성되어 있고 대부분 피막에 쌓여 있으며 분엽성, 압축성으로 서서히 자라나중에 경부혈관을 둘러싸 압박하게되며 그 이외 다른 혈관이나 신경을 누르게 된다. 경동맥체의 치료방법은 수술적 절제, 방사선 조사, 색 전술등이 알려져 있으며 이중 외과적 절제가 대표적인 치료 방법으로 알려져 있다. 하지만 외과적 절제가 쉽지 않고수술중비교적 높은 이병율과뇌혈류 부전으로 인한 반측마비등의 후유증을 유발할 수 있기 때문에 고도의 주의를 요한다. 저자들은 경동맥 체종양으로 진단받고 절제수술을 받은 2례를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Advances in pediatric surgery
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• 제2권1호
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• pp.64-67
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• 1996

1세된 남아에서 세열낭종을 의심한 좌측 경부 종양이 수술을 시행한 결과 고형종양이였고, 조직검사상 이소성 흉선으로 판명되었다. 술후 초음파상 흉선은 정상적으로 있었고, 현재 환자의 면역기능은 아무 이상없이 정상으로 자라고 있다.