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肾集合管癌10例临床及病理特征研究

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目的 探讨肾集合管癌(CDC)的临床及病理特征。方法 选取2017年3月至2023年3月该院收治的10例CDC患者的临床、病理资料,对其进行随访及相关文献复习。结果 10例CDC患者临床症状无特异性,以血尿及腰部疼痛为主,部分伴尿频尿急、夜尿增多;肿瘤位于左、右侧肾各5例;10例均行肾脏根治性切除术。组织学上,肿瘤浸润性生长,肿瘤细胞呈管状、乳头状、巢团状或实性片状排列,或肉瘤样排列,管腔内部分肿瘤细胞呈靴钉样凸向腺腔;肿瘤细胞具有高级别核,细胞异型明显,核大,核仁明显,核分裂象易见;间质纤维组织增生明显伴较多炎细胞浸润;多数病例中见肿瘤坏死。免疫组化结果CK、CK7、CK19、Pax-8阳性,Vimentin、EMA、34βE12、CarbonicA Ⅸ 不同程度阳性,RCC、CD10、CD117、TFE3、TFEB、P504S、CK20 均阴性;Ki-67增殖指数20%~70%。7例获得随访,3例失访;截至随访日期,仅1例存活,6例均于2年内死亡。结论 CDC是一种非常少见的肾上皮恶性肿瘤,恶性程度高,病程进展快,预后差。
Clinical and pathological features of renal collecting duct carcinoma:a study of 10 cases
Objective To investigate the clinical and pathological features of renal collecting duct carci-noma(CDC).Methods Clinical and pathological data of the 10 CDC patients diagnosed from 2017 to 2023 in this hospital were collected,followed up and relevant literatures were reviewed.Results The clinical symp-toms of the 10 CDC patients were non-specific,mainly hematuria and lower back pain,and some were accom-panied by frequent urination,urgency,and increased nocturia;The tumors of five cases were located in the left kidney and the others were located in the right kidney;All the 10 cases underwent radical nephrectomy.Histo-logically,the tumor underwent infiltrative growth,with tumor cells arranged in tubular,papillary,nested,or solid patches,or in a sarcomatoid manner.Some tumor cells within the lumen protruded into the glandular cavity in a shoe like manner;Tumor cells had high-grade differentiated nuclei,obvious cell abnormalities,large nuclei,prominent nucleoli,and mitotic figures were easily visible;Interstitial fibrous tissue hyperplasia was with significant infiltration of inflammatory cells;Tumor necrosis was seen in most cases.Immunohistochemi-cal results showed positive expression of CK,CK7,CK19,Pax-8,and Vimentin,EMA,34βE12 and CarbonicaⅨ were positive to varying degrees,while RCC,CD10,CD117,TFE3,TFEB,P504S,and CK20 were all nega-tive;The proliferation index of Ki-67 was 20%-70%.Seven cases were followed up,and three cases were lost;At the date of the last follow-up,only one case survived,and six cases all died within two years.Conclu-sion CDC is a very rare renal epithelial malignancy with high malignancy,rapid progression,and poor prog-nosis.

KidneyCollecting duct carcinomaHistologyImmunohistochemistryDifferential diagnosis

乔娟、王美玲、王弦、秦蓉、冯振中、吴继锋

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安徽医科大学第二附属医院病理科,安徽合肥 230601

集合管癌 组织学 免疫组化 鉴别诊断

2024

现代医药卫生
重庆市卫生信息中心

现代医药卫生

影响因子:0.758
ISSN:1009-5519
年,卷(期):2024.40(3)
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