• 제목/요약/키워드: Minor salivary gland tumor

검색결과 61건 처리시간 0.033초

주침샘의 병변 없이 경부림프절에 발생한 Warthin씨 종양 1예 (A Case of Solitary Warthin's Tumor from Cervical Lymph Node)

  • 이용수;박지수;나기상;구본석;장재원
    • 대한두경부종양학회지
    • /
    • 제31권2호
    • /
    • pp.39-42
    • /
    • 2015
  • Warthin's tumor is the second most common salivary gland benign tumor, typically occurring in the fifth to seventh decades of life which shows an indolent feature. It is usually found in the parotid gland but occasionally in extra-parotid locations such as peri-parotid lymph node. However, Report of solitary Warthin's tumor in cervical lymph node is unusual. We here report a case of 72-year-old male with simultaneous malignant melanoma on eyelid and cervical lymph node enlargement in cervical level II area thus mimicking malignancy metastasis. After excisional biopsy under the local anesthesia, pathology was reported as papillary cystadenoma lymphomatosum, which is a histologically pathognomic finding of Warthin's tumor. However, there was no suspicious tumorous lesion in major or minor salivary glands. This case suggests that Warthin's tumor should be considered as a possible pathology in solitary lymph node lesion of neck.

  • PDF

누액선에 발생한 Adenoid Cytic Carcinoma - 증 례 보 고 - (Lacrimal Gland Adenoid Cystic Carcinoma - A Case Report -)

  • 서대희;백정환;김윤덕;하범준;박익성;남도현;박관;김종현
    • Journal of Korean Neurosurgical Society
    • /
    • 제29권8호
    • /
    • pp.1089-1093
    • /
    • 2000
  • Adenoid cystic carcinoma(ACC) is a rare malignant tumor that occurs in exocrine glands such as major and minor salivary glands, lacrimal glands, ceruminal glands. It has a tendency for delayed distant metastasis and long clinical course. ACC of the lacrimal gland is generally found in adults and is usually managed by radical orbitectomy and supplemental external beam irradiation. The authors present two cases of recurrent lacrimal gland ACC with review of the literature.

  • PDF

경부 종괴의 임상 및 병리학적 고찰 (A Clinicopathologic Analysis of Neck Masses)

  • 김정호;오상훈;김상효
    • 대한두경부종양학회지
    • /
    • 제13권1호
    • /
    • pp.51-57
    • /
    • 1997
  • A mass appearing in the anterior or lateral side of neck often can be a diagnostic challenge. Differential diagnosis of the neck mass covers a broad spectrum of diseases and the proper evaluation and management of a neck mass requires an impressive amount of anatomic and pathologic information. Because improper diagnosis and management may convert a potentially curable malignant metastasis into incurable disease, a differential diagnosis must be considered in all patients who present with a neck mass. Authors reviewed 2,148 cases of neck mass who were diagnosed by surgical resection, biopsy or aspiration during the period between October 1982 to December 1993, excluding those with thyroid and parathyroid disease. The evaluated characteristics were age, sex, site of lesion, and pathologic diagnosis. The results were as follows: Of 2,148 cases of neck mass, the overall ratio of benign to malignant tumor was 3 : 1. In 1,603 cases of benign mass lesion, the most common disease was lymphadenitis(non-specific and tuberculosis) showing 53% incidence, the second was salivary gland tumor(13%), and the third was congenital lesion(12%). The minor problems such as lipoma and sebaceous cyst were 21 %. In the age distribution of benign lesion, tuberculous lymphadenitis showed peak incidence in second decade, non-specific lymphadenitis was main disease of childhood, salivary gland tumor was peak in fourth decade, and most of congenital lesions were diagnosed at the age below 15. In 545 malignant tumors, the most common lesion was metastatic cancer to cervical lymph nodes yielding 71 % incidence(head and neck primary 52%, infraclavicular primary 42%, unknown primary 5%), the second common disease was lymphoma(19%), and the third was salivary gland cancer(9%). In the age incidence of malignant tumor, 60% of them developed in the fifth and sixth decade, head and neck primary was more common in the fifth decade than sixth, however lymphoma showed higher incidence in sixth decade. In the analysis of mass location according to lymph node level grouping(I - V), lymphadenitis developed mostly in level V nodes, the next common occurring site was level IV in tuberculous lymphadenitis and level II in non-specific lymphadenitis. The majority of metastatic cancers were found in level IV and III, and common occurring site of lymphoma was in level II and IV. Pathologic diagnosis of neck masses were made by fine needle aspiration cytology 80 cases, incisional biopsy 533 cases, excisional surgery 1,399 cases, and neck dissection 116 cases. For the proper management of neck mass, a proper diagnostic modality should be selected from imaging techniques, cytology, biopsy or neck dissection, with the consideration of patient's age, history and clinical findings. The scapel biopsy could be used freely in the inflammatory disease or inoperable metastatic cancer, but it should be reserved in the curable metastatic cancer or clinically possible malignancy.

  • PDF

두경부의 Adenoid Cystic Carcinoma (Adenoid Cystic Carcinoma of the Head and Neck)

  • 박준식;설대위
    • 대한기관식도과학회:학술대회논문집
    • /
    • 대한기관식도과학회 1981년도 제15차 학술대회연제순서 및 초록
    • /
    • pp.14.2-14
    • /
    • 1981
  • 1859년 Billroth가 부비동에 발생한 종양을 "Zylindrome" 이라고 처음 명명한 이후 cylindroma, basaloma, basaloid adenoma, cribriform adenocarcinoma등으로 일컬어져 왔다. 그러나 최근에는 adenoid Cystic carcinoma라고 널리 사용되고 있다. 이 종양은 주로 두경부의 타액선에서 발생하고 있으나 그외 기관, 폐, 유방, 피부 등에서도 드물게 생긴다고 한다. 이 종양은 근치수술과 같은 광범위한 외과적 절제후에도 국소재발이나 원격전이가 많으며 방사선 치료로서 완전치유는 불가능 하나 종양의 축소와 동통의 소실등 경감치료에 좋은 효과를 보여 주는 것이 그 특징이다. 저자들은 1963년 1월부터 1980년 l2월까지 전주 예수병원에서 진단받은 adenoid cystic carcinoma 44례에 대하여 분석 검토하여 다음과 같은 결과를 얻었다. 1) 동기간의 두경부 악성종양중 3.8%를 차지하며 타액선 악성종양중 40%였었다. 2) 가장 흔한 원발장소는 구개, 악하선으로 각각 8례이며 그외 상악동이 6례 비강이 5례, 이하선, 설부위가 각각 4례였다. 3) major gland가 13례(31%), minor gland가 29례 (69%)였 다. 4) 성별은 남자 21례, 여자 23례로 남여의 차이는 거의 없었다. 5) 연령빈도는 19세에서 78세 사이로 평균 연령은 50세 였다. 6) 초친시 종양의 크기는 4∼6cm가 10례로 가장 많으며 임상적 경부 임파전이가 7례, 원격전이가 1례 였다. 7) 27례에서 근치수술을 시행 하였으며 이 중 14례는 수술과 방사선 병용 요법을 시행하였다. 8) 추적 관찰이 가능 하였던 29례에서 gross 3-year survival은 27.6%, determinate 3-year survival은 44.4%였다. 이 중 근치수술 받은 12례 있어서 3-year survival rate는 58%였다. 9) 29례중 10례에서 치료후 국소 재발을 보였다. 치료와 국소 재발 간의 기간은 3개월에서 88개월이며 이중 3례는 5년 이후였다. 10) 치료후 원격전이를 보인 것은 3례이며 전이장소는 모두 폐 였다.

  • PDF

악하선 절제술의 임상적 연구 (A CLINICAL STUDY OF SUBMANDIBULAR GLAND EXCISION)

  • 정인교;김종렬;김욱규;신상훈;김용덕;변준호;박봉욱;장원석
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • 제30권6호
    • /
    • pp.545-550
    • /
    • 2004
  • Salivary glands, major and minor, are susceptible to a wide variety of pathologic conditions. Excision of the submandibular gland is a surgical procedure often undertaken. The procedure is the treatment of choice for patients with neoplasm of the submandibular gland and those with non-neoplastic submandibular disorders which are not controlled with conservative medical measures. Extirpation of the submandibular gland may also be undertaken for diagnostic purposes. We evaluated 84 patients who had been admitted to the dept. of oral and maxillofacial surgery of Pusan National University Hospital from January, 1989 to December, 2002 and had been performed submandibular gland excision. The results are as follows : 1. The patients undertaken the excision of the submandibular gland showed an age range of 16 to 71 years. The average was 49.1. 2. They consisted of 60 males(71.4%) and 24 females(28.6%), having 2.5 : 1 of genda ratio. 3. The most common symptom was swelling in 41 cases(48.8%), followed by the pain in 23 cases(27.4%). Other symptoms included mass, dysphagia, facial abnormaly and neck dyscinesia. 4. 42 cases(50.0%) showed sialadenitis and sialodochitis associated with salivary calculus. 5. According to the histopathologic study, all cases consisted of 17 neoplasmatic conditions(20.3%) and 67 non-neoplasmatic(79.7%). The neoplasmatic cases included 13 benign tumors and 4 primary malignant tumors. Sialadenitis and sialodochitis associated with or without salivary calculus were most marked, found in 50 cases(59.3%), in the non-neoplasmatic conditions. Pleoomorphic adenoma showed the highest frequency of the benign tumor.

악성 타액선 종양의 방사선 치료 성적에 대하여 -원자력 병원의 10년 경험 ($1975.1{\sim}1984.12$)- (Primary Radiation Therapy of Malignant Salivary Gland Tumors by Conventional Megavoltage Irradiation -Korea Cancer Center Hospital-)

  • 조철구;고경환;류성렬;박영환;박우윤;심윤상;오경균
    • Radiation Oncology Journal
    • /
    • 제8권1호
    • /
    • pp.35-43
    • /
    • 1990
  • 1975년 1월부터 1984년 12월까지 원자력병원 치료 방사선과에서 악성 타액선 종양으로 방사선 치료를 받은 58명의 환자를 대상으로 하여 이들의 생존율을 후향적으로 분석하였다. 이들은 수술후 재발했거나, 수술이 불가능한 환자들이었다. 58명의 환자중 mucoepidermoid carcinoma를 가진 환자가 $43.1\%$, adenoid cystic carcinoma를 가진 환자는 $41.3\%$였다. 주 타액선 종양의 5년 보험생존율은 $68.2\%$, 10년 생존율은 $31.8\%$였으나, 무병생존율은 각각 $43.2\%\;13.0\%$로써 치료 후 재발된 상태에서도 비교적 오래 산다는 것을 알 수 있었다. TNM staging에 의한 생존율도 $T_1$의 5년 생존율이 $86.5\%,\;T_2+T_3$$40.0\%,\;T_4$$0\%$로, T stage가 높아지면 질수록 생존율도 현저히 감소하였다. 병리조직학적 관점에서 볼 때, adenoid cystic carcinoma의 5년 무병생존율은 $40.1\%$로써, mucoepidermoid ca.의 $49.8\%$보다 낮았으나, 전체적인 생존율은 $77.3\%$로써, mucoepidermoid ca.의 $51.5\%$보다 현저히 높았다. 따라서, adenoid cystic carcinoma는 치료실패후 병을 가진 상태에서도 상당 기간 생존할 수 있다는 것을 알았으며, 평균 생존기간은 2년 이었다. 또한 mucoepidermoid ca.인 경우에는 세포의 분화정도에 따라 생존율이 달라졌는데, 저등도 분화세포의 5년 생존율이 $78.8\%$로 고등도 분화세포의 $38.2\%$보다 거의 2배나 높았다. 암의 위치와 성별에 따른 생존율의 차이는 없었다. Minor salivary gland tumor는 6명으로 5년 보험생존률은 $32.3\%$였다. 따라서 주 타액선 종양의 생존율에 영향을 끼칠 수 있는 예후 인자는 1) 병리조직학적 세포종류, 2) T와 N stages (AJCC), 3) mucoepidermoid carcinoma에 있어서 분화 정도 였다.

  • PDF

기관지 선종의 외과적 치료[17례 보고] (Surgical Treatment of Bronchial Adenoma - Reports of 17 Cases -)

  • 문석환
    • Journal of Chest Surgery
    • /
    • 제25권3호
    • /
    • pp.247-257
    • /
    • 1992
  • Bronchial adenoma, firstly described by Muller[1882] had been reported on the subject stressed their benign nature prior to 1940`s, but these tumors including carcinoid tumor, mucoepidermoid carcinoma, adenoid cystic carcinoma, pleomorphic adenoma are now known to possess the various degree of malignant natures from benign course, low grade malignant potential to distant lymphatic or hematogenous metastasis or combination. Although histologically diffeerent, four varieties except carcinoid tumor which is a spectrum of neu-roendocrine tumor originating Kulchitsky cell of the bronchial epithelium and form the part of the APUD tumor spectrum, are morphologically and in many respects clinically similar to the corresponding tumor of the salivary gland is a specific varient of adenocarcinoma that occurs most commonly in the major and minor salivary gland and less frequently tra-cheobronchial tree, esophagus etc. To better understand the clinical characteristics and assess more precisely the malignat nature of bronchial adenoma, we studied 17 cases of bronchial adenoma, which had been experienced at the Department of Thoracic and Cardiovascular surgery of Catholic University Medical College from April 1977 to september 1991. Seventeen cases of bronchial adenoma consist of 2 carcinoid tumors, 6 adenoid cystic carcinomas, 8 mucoepidermoid carcinomas and one pleomorphic adenoma. There is a slight predominace of male patients[10/17] and the age of pt studied varied with a higher incidence occurring between the ages of 40 years and 60 years[mean age, 46.5 years]; the youngest being 15 years and oldest 69 years. Their leading complaints were hemoptysis[4], exertional dyspnea[8], fever & chilness [4], and symptoms mimicking the bronchial asthma[4]. Diagnosis was aided by the radiologic studies such as chest X-ray, polytomography, CT scan, brochography and bronchoscopy. The preferred locations of fumor were in the trachea[4], main stem bronchus[3], bronchus intermedius[3], bronchus of RUL[2], LUL[1], RLL[1], LLL[3] with no peripheral location. Modalities of treatments were single or combination of surgical resection, radiation therapy, chemotherapy. Complete resections were permitted in 12 cases with late recurrences of 4 cases ranging from 6 months to 10 years: pneumonectomy[4], lobectomy[4], bil-obectomy[2], sleeve resection[2]. Gross findings of resected specimens in 14 cases showed that 4 cases were polyp-like pedunculated mass[entirely intraluminal mass] with intact mucosa, 8 cases were broad-bas-ed sessile mass[predominatly intraluminal] and the main portions were located below the mucosa similar to tip of iceburg[predominantly extraluminal] in 2 cases. Follow-up information was availble in all 17 cases ; eight were alive without evidence of disese ranging from 1 month to 13 years. But seven cases died of the causes related to tumor[6 cases within 12 months, one case 10 years after pneumonectomy]. We concluded that 8 cases[47%] of 17 cases were metastasizing bronchial adenoma and precise survival rate cannot be answered by the scanty materials available for study.

  • PDF

Angioleiomyoma of the oral cavity: a case report and brief review of the literature

  • Matiakis, Apostolos;Karakostas, Panagiotis;Pavlou, Achilleia-Maria;Anagnostou, Eleftherios;Poulopoulos, Athanasios
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • 제44권3호
    • /
    • pp.136-139
    • /
    • 2018
  • This study presents a case of an oral angioleiomyoma along with its clinical diagnostic approach and laboratory confirmation. The differential diagnosis, especially from angioleiomyosarcoma, is also included. A 51-year-old patient presented with a tumor-like lesion on his upper labial mucosa. The clinical examination revealed a benign lesion that was surgically removed. Histopathological and immunohistochemical examinations confirmed the diagnosis of an oral angioleiomyoma. The post-surgical period was uneventful. No recurrence had occurred after a year of follow-up surveillance. Oral angioleiomyoma is a very rarely occurring oral lesion. Clinically, it may mimic some benign lesions, including fibroma, pyogenic granuloma or minor salivary gland tumor. Surgical excision is the treatment of choice. Histological and immunohistochemical examination can confirm the diagnosis. The differential diagnosis is crucial to rule out angioleiomyosarcoma.

구개부에 발생한 다형성 저등급 선암종의 치험례 (Polymorphous low-grade adenocarcinoma on hard palate: case report)

  • 신영민;최소영;김진욱;변기정;김진수
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
    • /
    • 제37권1호
    • /
    • pp.72-76
    • /
    • 2011
  • Polymorphous low-grade adenocarcinomas (PLGA) are distinctive salivary gland neoplasms with a propensity to arise from the minor salivary glands. The most frequent location of PLGA is the palate, even though other locations have been described. Previously used terms for PLGA include lobular carcinoma and terminal duct carcinoma. Although the frequency of the tumor is unknown, the recognition of PLGA as an individual tumor has increased with the establishment of specific histopathological criteria characterizing the PLGA. The first choice of treatment is a wide surgical excision including the subjacent bone if necessary. The prognosis is generally good and the recurrence rate ranges from 17% and 22%. Distant metastases is unusual (9%) but occur mainly in the regional lymph nodes. This is a case report of a 67 year old female patient with PLGA who was treated with a wide excision by layers (2 stage) of the lesion including the surrounding bone. We present this case with a review of the relevant literature.

다형성 선종의 치험 및 병리조직학적 연구 (TREATMENT AND PATHOLOGIC STUDY OF PLEOMORPHIC ADENOMAS)

  • 김일규;이성준;하수용;주영채
    • Maxillofacial Plastic and Reconstructive Surgery
    • /
    • 제13권2호
    • /
    • pp.167-176
    • /
    • 1991
  • 저자등은 우측 이하선(46 세 여)과 우측 및 좌측 협점막의 소타액선(67 세 여, 28 세 여)에서 발생한 세 증례의 다형성 선종 환자에서, 우측 이하선 전적출술(증례 1) 및 종양 완전적출술 (증례 2, 3)로 치험하고 병리조직학적 검사 결과 다음과 같은 결론을 얻었다. 1. 안면신경의 보존을 위해 하악지에서 역행하여 본관에 접근하였으며, 수술 직후에 발생한 우측 하순 운동마비 증상은 3 개월 경과후 완전히 회복된 소견을 관찰하였다. 2. 현미경학적으로, 증례 1 에서는 myxoid 와 cellular 성분의 구성비율이 거의 같았으며 완전한 피낭형성을 보였다. 3. 증례 2 에서는 출혈, 낭포성 변화, 이영양성 석회화, 지질의 초자질화 소견이 관찰되었으나, 결정적인 악성 종양의 소견은 관찰되지 않아 "Atypical mixed tumor"로 분류하였다. 4. 증례 3 에서는 대부분 myxoid 한 조직으로 구성되었으며 블완전한 피막을 보였으나, 정상적인 선조직과의 경계는 명확하였다.

  • PDF