• 제목/요약/키워드: Neuroendocrine cell carcinoma

검색결과 62건 처리시간 0.02초

상악동에 발생한 대세포 신경내분비 암종 1례 (A Case of Large Cell Neuroendocrine Carcinoma of the Maxillary Sinus)

  • 이윤재;정진혁;오영하;지용배
    • 대한두경부종양학회지
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    • 제35권2호
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    • pp.45-49
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    • 2019
  • Large cell neuroendocrine carcinoma is a rare epithelial neuroendocrine malignancy and is preferentially located in gastrointestinal tract and pancreas. Cases of large cell neuroendocrine carcinoma have been reported in many other locations, including the thymus, gallbladder, prostate, larynx, salivary glands, nasopharynx, tonsil and mastoid. However, primary sinonasal large cell neuroendocrine carcinoma never have been reported in Korea. We experienced a case of primary large cell neuroendocrine carcinoma arising from left maxillary sinus recently. A 82-year-old male patient presented with nasal obstruction and epistaxis. The biopsy revealed large cell neuroendocrine carcinoma with poor differentiation. After a general evaluation, the patient was staged as cT3N0M0. The patient was treated by combined radiotherapy and chemotherapy. We report this rare case with literature review.

대세포 신경내분비암-1례 보고- (Large Cell Neuroendocrine Carcinoma of the Lung - A case report -)

  • 김연수;류지윤;김민경;장우익;김욱성
    • Journal of Chest Surgery
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    • 제35권12호
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    • pp.909-913
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    • 2002
  • 대세포 신경내분비암은 드문 질환으로, 최근에 폐의 신경내분비암의 하나로 진단 기준이 확립되었다. 심한 흡연자로 증상이 없는 74세의 남자가 우하엽의 종양을 주소로 내원하였다. 세침 생검을 통해 대세포 신경내 분비암으로 진단되었다. 우하엽 절제술과 종격동 림프절 곽청술을 시행 받았다. 저자들은 대세포 신경내분비암의 한 례를 치험하였고 문헌고찰과 함께 보고한다.

하인두에 발생한 신경내분비성 소세포암종 1예 (A Case of Neuroendocrine Small Cell Carcinoma Arising from the Hypopharynx)

  • 고윤우;이종대;변장열;이재용
    • 대한두경부종양학회지
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    • 제20권2호
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    • pp.198-201
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    • 2004
  • Neuroendocrine carcinomas are rare neoplasms of the hypopharynx. Neuroendocrine neoplasms are divided into four main types : carcinoid, atypical carcinoid, small cell carcinoma and paraganglioma. The diagnosis is primarily based on light microscopy and should be confirmed by immunohistochemical investigation. Small cell neuroendocrine carcinoma of the hypopharynx is extremely uncommon tumor and surgical results for this tumor have been disappointing. Chemotherapy and radiotherapy currently appear the most effective forms of therapy. We report our case of small cell neuroendocrine carcinoma of the hypopharynx with the brief review of literatures.

대세포 신경내분비암 -1례 보고- (Large Cell Neuroendocrine Carcinoma of the Lung -A Case Report-)

  • 김영진;김범경
    • Journal of Chest Surgery
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    • 제35권4호
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    • pp.311-314
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    • 2002
  • 간헐적 우측 흉부 동통을 호소하는 48세 남자 환자로 단순 흉부 방사선 촬영상 우측 중폐야에 거대 종괴가 관찰되어 우측 쌍폐엽 절제술 후 대세포 신경 내분비 암으로 진단되어진 1예를 치험 하였기에 문헌 고찰과 함께 보고하는 바이다.

Multiregion Comprehensive Genomic Profiling of a Gastric Mixed Neuroendocrine-Nonneuroendocrine Neoplasm with Trilineage Differentiation

  • Farooq, Faheem;Zarrabi, Kevin;Sweeney, Keith;Kim, Joseph;Bandovic, Jela;Patel, Chiraag;Choi, Minsig
    • Journal of Gastric Cancer
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    • 제18권2호
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    • pp.200-207
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    • 2018
  • Mixed neuroendocrine-nonneuroendocrine neoplasms (MiNENs) are a group of rare tumors previously known as mixed adenoneuroendocrine carcinomas (MANECs). The neuroendocrine component is high-grade and may consist of small-cell carcinoma or large-cell neuroendocrine carcinoma. The nonneuroendocrine component may consist of adenocarcinoma or squamous cell carcinoma. We report a unique case of a MiNEN with trilineage differentiation: large-cell neuroendocrine carcinoma, squamous cell carcinoma, and adenocarcinoma. The reported patient presented with symptoms of an upper gastrointestinal bleed and was ultimately diagnosed with a MiNEN with trilineage differentiation. This is the first report of this exceedingly rare tumor type to include next-generation sequencing of the 3 separate tumor entities. In addition, we review the current literature and discuss the role of next-generation sequencing in classifying and treating MiNEN tumors.

폐의 대세포 신경내분비암 -1례 보고- (Pulmonary Large Cell Neuroendocrine Carcinoma -One Case Report-)

  • 이석열;송철민;조현득;박형주;이철세;이길노
    • Journal of Chest Surgery
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    • 제35권12호
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    • pp.906-908
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    • 2002
  • 전신쇄약을 주소로 내원한 60세 남자환자가 흉부 방사선 사진상 좌폐하엽에서 폐종양이 발견되었다. 좌폐하엽절제술과 종격동 임파선 절제를 시행후 병리조직검사상 폐의 대세포 신경내분비암으로 진단되었다. 폐의 대세포 신경내분비암은 드문 질환으로 저자들은 이를 치험하였기에 보고하는 바이다.

A Case of Gastric Large Cell Neuroendocrine Carcinoma with Multiple Liver Metastasis Treated with Hepatic Artery Infusion Chemotherapy Followed by Surgery

  • Sung Bum Kim;Kook Hyun Kim;Tae Nyeun Kim
    • Journal of Digestive Cancer Research
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    • 제3권1호
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    • pp.26-29
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    • 2015
  • A 73-year-old male visited our hospital with a complaint of general weakness. He underwent pyloric preserving pancreas-toduodenectomy due to ampullary cancer three years ago. Abdominal computed tomography scan at initial visit revealed multiple hepatic masses. A PET-CT scan showed multiple FDG uptakes at whole liver. He underwent hepatic artery infusion chemotherapy (HAIC) for five cycles. During the first cycle of HAIC, he developed gastric ulcer bleeding and endoscopic hemostasis was done successfully. Esophagogastroduodenoscopy after the 5th cycle of HAIC revealed ulcer scar at gastric angle. PET-CT scan at 12 months showed no FDG uptake at liver, but a focal FDG uptakes at stomach and peri-gastric lymph nodes were newly developed. Esophagogastroduodenoscopy revealed about 3 cm sized mass at gastric angle. He underwent surgery and pathologic examination revealed large cell neuroendocrine carcinoma. We report a case of gastric large cell neuroendocrine carcinoma with liver metastasis treated with HAIC followed by surgery.

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선암종의 요소를 갖느느 혼압대세포신경내분비암종-1예 보고- (Combined Large Cell Neuroendocrine Carcinoma with Component of Adenocarcinoma-A case report-)

  • 박종운;이재웅;조태준;김건일;이원용;홍기우;엄광석;전선영
    • Journal of Chest Surgery
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    • 제38권8호
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    • pp.579-582
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    • 2005
  • 혼합대세포신경내분비암종은 매우 드문 폐암으로, 조직학적으로 대세포신경내분비암종의 종양세포외에 선암종, 편평세포암종, 거대세포암종 혹은 방추상암종의 구성세포를 포함한다. 저자는 간헐적 흉부 동통을 호소하는 44세 남자환자가 우측 중폐야의폐종양으로 내원하여서 시행한 우측 폐전적 출술과 종격동 림프절 곽청술 후 병리에서 선암종의 요소를 갖는 혼합대세포신경내분비암종이 진단되어 문헌고찰과 함께 보고하는 바이이다.

자궁 경부의 선암과 혼합된 신경내분비 소세포 암종 - 1 증례 보고 - (Composite Tumor of Adenocarcinoma and Small Cell Neuroendocrine Carcinoma of the Uterine Cervix -A Case Report-)

  • 박혜림;이용우;박영의
    • 대한세포병리학회지
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    • 제1권1호
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    • pp.111-120
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    • 1990
  • Small cell neuroendocrine carcinoma of the uterine cervix is a distinct subtype of cervical cancer that appears analogous to oat cell carcinoma and carcinoid tumors of the lung. It has been assumed to be derived from the neural crest via argyrophilic cells in the normal endocervix. We have recently encountered a case of small cell neuroendocrine carcinoma of the uterine cervix coexisting with adenocarcinoma which was argyrophil negative. A 66-year-old multiparous woman was admitted because of vaginal bleeding for 2 months. Cervicovaginal smear revealed several scattered clusters and sheets of monotonous small cells with some peripheral palisading in the background of hemorrhage and necrosis. Radical hysterectomy specimen revealed an ulcerofungating tumor on endocervical canal which was composed of two components. Major component of the tumor was made up of monomorphic population of small oval-shaped tumor cells arranged in sheets and partly in acinar structures or trabecular fashion. Other component was adenocarcinoma, endocervical well-differentiated type. Argyrophilia was present on the Grimelius stain and immunohistochemical studies revealed diffuse positivity to neuron-specific enolase and carcinoembryonic antigen. Electron microscopic examination showed clusters of small round to oval cells, which had a few well-formed desmosomes and several membrane-bound, dense-core neurosectetory granules.

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폐의 신경내분비 종양의 세침흡인 세포검사 소견 (Fine Needle Aspiration Cytologic Findings of Pulmonary Neuroendocrine Tumors)

  • 고재수
    • 대한세포병리학회지
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    • 제19권1호
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    • pp.9-15
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    • 2008
  • The major categories of neuroendocrine tumors of lung are typical carcinoid, atypical carcinoid, large cell neuroendocrine carcinoma, and small cell carcinoma. The histologic classification criteria of neuroendocrine tumors are well documented in the "WHO Classification of Tumors" based on mitotic figures and necrosis. Cytologic characteristics of neuroendocrine tumors are trabecular, acinar, and solid arrangement of tumor cells and occasional rosette formation. Nuclear chromatin patterns are characteristically described as "salt and pepper chromatin pattern". Many of cytologic classifications documented in the literature are before the "WHO Classification". In this review, the cytologic features of pulmonary neuroendocrine tumors are documented according to the WHO classification, and recent concepts of neuroendocrine tumors of lung are discussed.