• 제목/요약/키워드: Neck tumor

검색결과 1,059건 처리시간 0.02초

두경부 편평상피세포암에서 종양억제유전자들의 변이 (Alteration of Multiple Tumor Suppressor Genes in Head and Neck Squamous Cell Carcinoma)

  • 송시연;박강식;배창훈
    • 대한두경부종양학회지
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    • 제20권2호
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    • pp.147-155
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    • 2004
  • Objectives: Head and neck squamous cell carcinoma (HNSCC) is the most common head and neck malignant tumor. The molecular genetic changes involving both oncogenes and tumor suppressor genes are known to be involved in head and neck squamous cell carcinogenesis, but the roles of the known tumor suppressor genes in carcinogenesis are not fully elucidated. The objectives of this study are to demonstrate the genetic alterations including the loss of heterozygosity (LOH) , amplification, and microsatellite instability of known tumor suppressor genes in HNSCC and to evaluate the relationship between genetic alterations of tumor suppressor genes and clinicopathologic features. Materials and Methods: Genetic alterations of 10 micro satellite markers of the 6 known tumor suppressor genes (APC, EXT1, DPC4, p16, FHIT, and PTEN) were analysed by DNA-PCR in paraffin-embedded histologically confirmed HNSCC specimens. Results: The genetic alterations of tumor suppressor genes were found frequently. Among the genetic alterations, LOH was most frequently found one. LOH was found frequently in APC (45.4%), EXT1 (36.4%), DPC4 (54.5%), and p16 (50%), but not found in FHIT. Also, the author found that abnormalities of APC gene was related to cervical lymph node metastasis and recurrence and that abnormalities of EXT1 gene were coexisted with those of APC gene or DPC4 gene. But these coexistences had no correlation with clinical features. Conclusion: These results suggested that APC, EXT1, p16, and DPC4 genes might play important roles and multiple tumor suppressor genes may participate dependently or independently in the carcinogenesis of HNSCC. These results also suggested that APC gene might relate to prognosis.

측경부에 발생한 이하선외 Warthin씨 종양 2예 (Two Cases of Extraparotid Warthin's Tumor in Lateral Cervical Region)

  • 최경민;양시창;김승우
    • 대한두경부종양학회지
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    • 제26권2호
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    • pp.232-235
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    • 2010
  • Extraparotid Warthin's tumor(EPWT) is a rare disease entity; its incidence is about 8% of Warthin's tumor(WT). The periparotid and upper cervical lymph nodes are the most predilection sites. The lymphoid tissue of WT can act like a regional lymph node, and the necrosis and inflammation within the tumor are well known. In our cases, both 81-year-old man and 58-year-old man were visited our clinic, presented with upper lateral neck mass that had been present for the last few months. We operated the excisional biopsy in level ll of neck. The pathologic examination was proven to be EPWT. We report the unique two cases of extraparotid Warthin's tumor with literature review.

신경성 종양으로 오인된 경부에 발생한 다형성 유리질 혈관확장성 종양 1례 (A Case of Pleomorphic Hyalinizing Angiectatic Tumor of Neck Mimicking Neurogenic Tumor)

  • 유석찬;여창기;신형찬
    • 대한두경부종양학회지
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    • 제36권2호
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    • pp.37-40
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    • 2020
  • Pleomorphic hyalinizing angiectatic tumor (PHAT) is a rare, low grade neoplasm which usually occurs in subcutaneous soft tissue. Histologically, it features ectatic blood filled vessels surrounded by hyalinized stroma and pleomorphic spindle cells. Clinically and histologically, PHAT could be misdiagnosed as such tumor as neurogenic tumor, malignant fibrous histiocytoma. About 100 cases of PHAT have been reported so far, and it is even rarer in head and neck area. We experienced a case of PHAT in 41-year-old male with several months of history of gradually enlarging neck mass which was surgically removed by wide excision.

부갑상선 종양으로 오인된 경부 식도 과립세포종 1례 (A case of granular cell tumor of the cervical esophagus misdiagnosed as parathyroid tumor)

  • 김동환;방성식;신수진;태경
    • 대한두경부종양학회지
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    • 제34권2호
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    • pp.81-84
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    • 2018
  • Granular cell tumor is an uncommon neoplasm that can occur everywhere in the human body. Granular cell tumor of the cervical esophagus is rare. Histopathologically, granular cell tumor consists of large polygonal cells with small dark nuclei and abundant, fine, granular eosinophilic cytoplasm that show positive immunohistochemical staining using S-100 protein. Surgical excision is the treatment of choice for granular cell tumor. Recurrence is rare, but inadequate resection of granular cell tumor may cause local recurrence. We have experienced one case of granular cell tumor of the cervical esophagus that was misdiagnosed with parathyroid tumor. Therefore, we report it with the literature review.

경부 전이성 이하선암과 유사한 양상의 이하선내외에 동시 발생한 편측성 왈틴씨 종양 1예 (Unilateral Synchronous Intra-and Extra-Parotid Warthin's Tumor, Presenting as a Similar Pattern of Cervical Metastasis from Parotid Cancer : A Case Report)

  • 사대진;곽슬기;김춘동;김승우
    • 대한두경부종양학회지
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    • 제29권1호
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    • pp.11-13
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    • 2013
  • Warthin's tumor is the second most common tumor of the parotid gland after pleomorphic adenoma. It is well known to occur as bilateral and multiple patterns. The incidence of extraparotid Warthin's tumor (EPWT) is about 2.7% to 12%, peri-parotid and upper cervical area are the most common sites. Warthin's tumor with synchronous intraparotid and extraparotid area is extremely rare, only a few cases have been reported. We report a-71-year old man with unilateral swelling of the parotid area and upper neck, pathologically confirmed Warthin's tumor with literature review.

경부에서 발견된 비정형 지방종성 종양 1예 (A Case of Atypical Lipomatous Tumor of the Neck)

  • 노영진;이동근;박헌수
    • 임상이비인후과
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    • 제29권2호
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    • pp.286-289
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    • 2018
  • Liposarcoma is a malignant tumor that occurs in adipocytes, accounting for 5% of all sarcomas. Generally, it has no symptoms and it occurs in any parts of the body. There are various types of liposarcoma. Of these, 40-45% are known as highly differentiated liposarcoma, and highly differentiated liposarcoma is also referred to as atypical lipomatous tumor. We report a case of an atypical lipomatous tumor on the left neck.

두경부암(頭頸部癌)에서 중성자선(中性子線) 치료(治療)의 효과(?果) (The Effect of Neutron Therapy on Head and Neck Cancer)

  • 유성렬;고경환;조철구
    • 대한두경부종양학회지
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    • 제5권1호
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    • pp.31-38
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    • 1989
  • The result of neutron therapy on head and neck cancer using KCCH -Cyclotron neutron which had been using from October 1986 to September 1989 in the Korea Cancer Center Hospital. Among the total of 27 patients the cases of malignant salivary gland tumor were 14 and the cases of advanced head and neck cancer of AJCC stage IV were 13. The local control rate was 80% in malignant salivary gland tumor and 46.2% in advanced head and neck cancer. The 2 year survival rate was 60% in malignant salivary gland tumor and 38.5% in advanced head and neck cancer. Although there was no significant difference in prognosis according to the pathologic types, squamous cell carcinoma revealed a pattern of poor prognosis. The major complication from the neutron therapy had developed 7.1% in malignant salivary gland tumor and 23.1% in advanced head and neck cancer. In conclusion, neutron therapy is superior in the treatment of malignant salivary gland tumor and also effective in the treatment of advanced head and neck cancer when it can avoid to treat some site of low tolerance.

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하경부 종물로 발현한 고립성 섬유종 1예 (A Case of Solitary Fibrous Tumor Presenting as Lower Neck Mass)

  • 금상연;김정규
    • 대한두경부종양학회지
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    • 제37권2호
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    • pp.87-90
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    • 2021
  • Solitary fibrous tumor (SFT) is rare mesenchymal tumor usually arising from pleura. SFT can be found at all anatomic site in our body but incidence of SFT is much lower in head and neck region especially at lower neck area. We found a case of SFT that presented as a lower neck mass in a 41-year old woman. Ultrasonography showed a 3×1cm sized hypoechoic mass in the intermuscular fat plane of left lower neck, and computed tomography showed a well circumscribed, low-density mass with contrast enhancement. Fine needle aspiration showed no malignant cells with abundant red blood cells, but it was not possible to completely rule out malignant tumors or nodules clinically. Surgery was performed to make a definitive diagnosis and histopathology showed tightly packed, round to fusiform cells with staghorn shaped vessels at microscopic examination. The tumor cell were positive for CD34 but negative for CD31 and S-100 protein.

육종성 변화를 동반한 경부의 염증성 근섬유모세포종 1례 (A Case of Malignant Transformation of Inflammatory Myofibroblastic Tumor of the Neck)

  • 김한결;최나연;배현식;박우리;정만기
    • 대한두경부종양학회지
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    • 제32권2호
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    • pp.55-59
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    • 2016
  • Iinflammatory myofibroblastic tumor(IMT) is a benign chronic inflammatory mass composed of proliferative myofibroblasts. It is a space occupying lesion which could potentially covert to malignant tumor. Treatment guideline of the disease has not been established due to its rarity. We demonstrate a 60-year old male who had surgical excision for IMT of the cervical esophagus. During the follow-up period, he revealed recurrent tumor which showed sarcomatous change with distant metastasis. We reported this rare case with review of the literature.

경부 유건종(Desmoid Tumor)의 방사선치료 - 증례보고 - (Radiation Treatment of Desmoid Tumor in the Neck - A Case Report­)

  • 표홍렬;신현수;김귀언;박정수
    • 대한두경부종양학회지
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    • 제7권1호
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    • pp.35-39
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    • 1991
  • A 66 years old female who had a huge desmoid tumor on her left neck was treated by partial excision and postoperative irradiation. Detailed summary of this rare tumor are included with a review of the literature about treatment modality including irradiation. We suggest that local irradiation is one of the effective treatment tools in the management of desmoid tumor, especially, in the case of unresectable or postoperative residual tumors on the neck.

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