肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2014年
10期
679-682
,共4页
程蔚蔚%李军红%周会行%魏素娇
程蔚蔚%李軍紅%週會行%魏素嬌
정위위%리군홍%주회행%위소교
阑尾肿瘤%类癌瘤%病理学,临床%免疫组织化学
闌尾腫瘤%類癌瘤%病理學,臨床%免疫組織化學
란미종류%유암류%병이학,림상%면역조직화학
Appendiceal neoplasms%Carcinoid tumor%Pathology,clinical%Immunohistochemistry
目的 探讨阑尾杯状细胞类癌(GCC)的临床病理特征、诊断标准及治疗预后.方法 分析郑州大学附属洛阳市中心医院6例GCC患者的临床病理资料.结果 6例患者平均发病年龄为48.67岁,临床上4例表现为急性阑尾炎的症状和体征,2例表现为腹部疼痛;手术方式:4例为阑尾单纯切除术,2例为阑尾切除术+右半结肠切除术;术后平均随访30个月,5例健康生存,1例失访.大体观察阑尾无明显肿块.显微镜下观察:4例肿瘤细胞似肠腺杯状细胞,无异型性和坏死,缺乏核分裂象,2例肿瘤细胞呈圆形及多边形,中等大小,胞质丰富,富含黏液,细胞核偏于一侧,呈印戒细胞样,瘤细胞呈巢状、花环状、腺样弥漫散在排列.免疫组织化学示:Syn阳性6例,CgA阳性4例,NSE、CD56、CK7、CK20均有患者阳性,5例Ki-67≤2%,1例Ki-67为3%,6例均未发现淋巴结、肠道、卵巢转移.结论 GCC是一种少见的神经内分泌肿瘤,较经典类癌更具有侵袭性.Syn、CgA阳性为诊断所必需的,Ki-67阳性指数对肿瘤分级有指导意义.
目的 探討闌尾杯狀細胞類癌(GCC)的臨床病理特徵、診斷標準及治療預後.方法 分析鄭州大學附屬洛暘市中心醫院6例GCC患者的臨床病理資料.結果 6例患者平均髮病年齡為48.67歲,臨床上4例錶現為急性闌尾炎的癥狀和體徵,2例錶現為腹部疼痛;手術方式:4例為闌尾單純切除術,2例為闌尾切除術+右半結腸切除術;術後平均隨訪30箇月,5例健康生存,1例失訪.大體觀察闌尾無明顯腫塊.顯微鏡下觀察:4例腫瘤細胞似腸腺杯狀細胞,無異型性和壞死,缺乏覈分裂象,2例腫瘤細胞呈圓形及多邊形,中等大小,胞質豐富,富含黏液,細胞覈偏于一側,呈印戒細胞樣,瘤細胞呈巢狀、花環狀、腺樣瀰漫散在排列.免疫組織化學示:Syn暘性6例,CgA暘性4例,NSE、CD56、CK7、CK20均有患者暘性,5例Ki-67≤2%,1例Ki-67為3%,6例均未髮現淋巴結、腸道、卵巢轉移.結論 GCC是一種少見的神經內分泌腫瘤,較經典類癌更具有侵襲性.Syn、CgA暘性為診斷所必需的,Ki-67暘性指數對腫瘤分級有指導意義.
목적 탐토란미배상세포유암(GCC)적림상병리특정、진단표준급치료예후.방법 분석정주대학부속락양시중심의원6례GCC환자적림상병리자료.결과 6례환자평균발병년령위48.67세,림상상4례표현위급성란미염적증상화체정,2례표현위복부동통;수술방식:4례위란미단순절제술,2례위란미절제술+우반결장절제술;술후평균수방30개월,5례건강생존,1례실방.대체관찰란미무명현종괴.현미경하관찰:4례종류세포사장선배상세포,무이형성화배사,결핍핵분렬상,2례종류세포정원형급다변형,중등대소,포질봉부,부함점액,세포핵편우일측,정인계세포양,류세포정소상、화배상、선양미만산재배렬.면역조직화학시:Syn양성6례,CgA양성4례,NSE、CD56、CK7、CK20균유환자양성,5례Ki-67≤2%,1례Ki-67위3%,6례균미발현림파결、장도、란소전이.결론 GCC시일충소견적신경내분비종류,교경전유암경구유침습성.Syn、CgA양성위진단소필수적,Ki-67양성지수대종류분급유지도의의.
Objective To explore the clinicopathologic features,diagnostic criteria and clinical prognostic factors of Goblet cell carcinoid (GCC) of the appendix.Methods The clinical and pathological data from 6 GCC patients were analyzed including age,clinical stage,surgical procedure,outcome,macroscopic features,histological sections and immunohistochemistry.Results The median age was 49.67 years old.Clinically,4 patients presented the signs and symptoms of acute appendicitis,while 2 patients presented the signs and symptoms of abdominal pain.4 patients of them undergone the simple appendectomy,the other 2 undergone the right hemicolectomy.All patients who had undergone the operation treatment survived.One patient was lost to the follow-up.Macroscopically,no masses were found in the appendix.Microscopically,4 cases showed that the tumor cells were identical to the goblet cell normal small intestinal crypts morphologically.The atypia,necrosis and mitotic figures of neoplasm cells were absent.2 cases were composed of small,discrete acini,tubules lined by a single layer of cuboidal or columnar cell,the signet-ring cells were uniform with pattern of infiltration being nests,rosrttes,or clumps without a dintinct lumen.All GCC cases were positive to Syn,4 cases were positive to CgA,some cases expressed NSE,CD56,CK7,CK20,Ki-67 index of 5 cases was under 2 %,the other 1 was 3 %.None had lymph node metastases,intestinal metastases or ovary metastases.Conclusions GCC of appendix is a rare neoplasm,and has more aggressive behaviour than classic carcinoids.Positive expression of Syn and CgA is necessory for the diagnosis of GCC,Ki-67 index may suggest the grading of tumor.