肾嗜酸性细胞瘤的诊治体会（附11例报告）

目的：探讨肾嗜酸细胞瘤的诊断和治疗。方法：回顾分析我院2003．2009年间收治11例肾嗜酸细胞瘤的临床资料,结合文献对肾嗜酸细胞瘤的诊断及治疗进行复习讨论。结果：本组11例患者中,年龄为26—75岁,男性7例,女性4例。合并透明细胞癌者1例,术前误诊为肾上腺肿瘤者1例。7例行根治性肾切除术者,4例行肾部分切除术。术后随访11个月-7年未见肿瘤转移或复发。结论：肾嗜酸细胞瘤倾向于良性肾实质性肿瘤,临床表现无特异性,确诊需临床表现、影像学检查与病理学检查相结合。治疗首选保肾手术,但应注意并发恶性肿瘤的可能,加强随访。     

肾嗜酸细胞腺瘤的诊疗分析（附47 例报告）

目的:分析肾嗜酸细胞腺瘤的临床特征,指导并提升诊疗水平。方法:回顾性分析47例肾嗜酸细胞腺瘤的临床资料,包括临床特点、影像表现、病理特征、治疗方法及预后等方面。结果:47例患者中43例因查体偶然发现,仅4例表现为患侧腰痛症状。术前影像诊断中1例考虑嗜酸细胞腺瘤,1例考虑腺瘤,2例CT与MRI报告不一致(CT与MRI各有1例诊断良性,具体类型不确定),其余43例均诊断为肾细胞癌(1例囊性肾癌)。27例行肾癌根治性切除术,16例行肾部分切除术,4例行微波或射频消融术。所有患者术后病理均诊断为肾嗜酸细胞腺瘤,随访4～179月,均无转移或复发。结论:肾嗜酸细胞腺瘤作为一种与肾细胞癌难相鉴别的良性肿瘤,因缺乏特异性表现,极易误诊为肾细胞癌,因此对肾肿瘤患者应尽可能选择保肾治疗方案。     

胰腺实性假乳头状瘤临床分析(附2例小儿和6例成人病例)

目的:探讨胰腺实性假乳头状瘤(solid pseudopapillary tumor of pancreas,SPTP)的诊断和治疗方法.方法:回顾性分析上海市第一人民医院在2006年6月-2011年11月年收治的8例SPTP病人的临床表现和影像学检查、治疗的情况,其中小儿2例,成人6例.结果:有7例女性病人,1例男性病人,有腹痛或无特异性临床表现.所有病例均进行CT检查.肿瘤位于胰腺头部1例,胰腺颈部2例,位于胰体尾5例.1例行胰十二指肠切除术,2例行胰腺颈部节段性切除术,4例行胰体尾切除+脾切除术,1例行胰体尾切除术(保留脾脏),手术顺利,术后无并发症发生.随访时间4-56月,无复发和转移.结论:胰腺实性假乳头状瘤是一种较罕见的肿瘤,多发于年青女性.CT有助于该病的诊断.手术切除是该病的主要治疗手段,并可获得良好的预后.     

胃间质瘤11例临床诊治分析

目的:探讨胃间质瘤(GST)的诊断和治疗措施.方法:回顾性分析我院2000年4月至2006年3月近6年收治的1I例胃间质瘤患者的临床表现、辅助检查、手术治疗方式及病理结果.结果:临床以消化道出血、腹部肿块表现为主,症状无特异性,所有病例术前均行胃镜及CT检查,均行手术治疗,其中6例行肿瘤楔形切除,5例行胃大部切除术,病理诊断良性5例(45.5%)交界性1例(9%),恶性5例(45.5%).随访时间3个月至5年,死亡1例,死于腹腔广泛转移.结论:胃间质瘤缺乏特异的临床表现,术前诊断困难,胃镜和CT可发现病变,诊断以病理诊断为准,其中免疫组化结果为重要诊断依据,治疗以手术切除为主.     

膀胱副神经节瘤的诊治分析(附1 例病例报告并文献复习)

目的:总结膀胱副神经节瘤的诊治方法及体会,提高膀胱副神经节瘤的诊断和治疗水平。方法:报告1例膀胱嗜铬细胞瘤的临床资料并结合文献复习分析总结膀胱副神经节瘤的诊断治疗方法。结果:患者行腹腔镜下膀胱部分切除术,手术成功,术后顺利出院,随访至今无转移。结论:膀胱副神经节瘤的诊断主要依靠临床表现和实验室检查,血尿、高血压和排尿时典型发作三联征为膀胱副神经节瘤的主要症状,对于瘤体较小的患者要警惕CT检查漏诊的可能性,可行活组织检查进行确诊。腹腔镜下切除是目前治疗膀胱副神经节瘤最有效、创伤最小的方法,但术后要严格随访。     

嫌色性肾细胞癌17例临床病理学分析

目的探讨嫌色性肾细胞癌的临床病理特征、诊断与鉴别诊断要点。方法对17例嫌色性肾细胞癌进行组织形态学、免疫组化染色及Hale’s胶样铁染色观察,结合文献对其临床表现、病理形态特点及鉴别诊断进行探讨。结果嫌色性肾细胞癌17例,大体肿瘤直径3-10.5cm。镜下肿瘤由嫌色细胞和嗜酸细胞构成,呈片状、梁状和腺泡状分布。嫌色细胞体积较大,多角形,胞膜清晰,胞质半透明细网状,胞核皱缩,可见核沟及核异型,核仁不明显;而嗜酸细胞胞质嗜酸,可见明显的核周空晕。免疫组化:EMA 100%阳性,CD10 52.9%阳性,Vimentin阴性,CK7 88.2%阳性,P504S29.4%阳性,CD11794.1%阳性。Hale’s胶样铁染色100%阳性。17例中12例随访6个月到3年,仅1例在术后15个月发现肝脏转移,其余均未发现复发及转移。结论嫌色性肾细胞癌是一种少见的肾肿瘤,恶性程度相对较低,预后良好。掌握该肿瘤独特的病理学特征,对鉴别其他肾上皮性肿瘤有重要帮助。     

肾嗜酸细胞腺瘤的影像学诊断

目的:探讨螺旋CT和MRI对肾嗜酸性细胞腺瘤的诊断及鉴别诊断的价值。方法:回顾性分析12例肾嗜酸性细胞瘤的CT和/或MRI表现。结果:CT检查12例,平扫8例病灶呈均匀软组织密度影,3例呈不均匀软组织密度影,1例瘤体周边有环状钙化。增强后病灶轻中度强化,6例见星状瘢痕。MRI检查3例,2例T1WI呈等低信号、T2WI呈高信号;1例T1WI呈等信号、T2WI等低信号。结论:多数肾嗜酸细胞腺瘤的影像学表现具有一定特征性。CT结合MRI特别是动态扫描有助于术前做出正确的诊断。     

睾丸间质细胞瘤3例报告及文献复习

目的:探讨睾丸间质细胞瘤的临床病理特点及诊疗方法。方法:分析并总结3例睾丸间质细胞瘤患者的临床病理资料并文献复习。结果:1例术中冰冻切片诊断为睾丸间质细胞瘤,2例术前细针穿刺病理诊断为睾丸间质细胞瘤,病理组织学表现为瘤细胞呈团、条索或弥漫分布,体积较大,呈多角形胞质丰富嗜酸性,边界清楚。2例患者行单侧睾丸切除,1例行睾丸肿瘤剜除术,术后分别随访24、15、10个月未见复发。结论:睾丸间质细胞瘤发病率低,临床表现缺乏特异性,易误诊,确诊需依赖病理组织学检查,细针穿刺病理可明确诊断并有助于手术的选择及手术范围的确定。     

肾嗜酸细胞腺瘤的影像学诊断

目的：探讨螺旋CT和MRI对肾嗜酸性细胞腺瘤的诊断及鉴别诊断的价值。方法：回顾性分析12例肾嗜酸性细胞瘤的CT和／或MRI表现。结果：CT检查12例,平扫8例病灶呈均匀软组织密度影,3例呈不均匀软组织密度影,1例瘤体周边有环状钙化。增强后病灶轻中度强化,6例见星状瘢痕。MRI检查3例,2例T1WI呈等低信号、T2WI呈高信号;1例T1wI呈等信号、T2WI等低信号。结论：多数肾嗜酸细胞腺瘤的影像学表现具有一定特征性。CT结合MRI特别是动态扫描有助于术前做出正确的诊断。     

嫌色性肾细胞癌与嗜酸细胞瘤的临床病理分析与比较

目的探讨嫌色性肾细胞癌(chromophobe renal cell carcinoma,CRCC)和嗜酸细胞瘤(oncocytoma)的临床病理学特征,提高对二者的认识和诊疗水平。方法对手术切除的5例CRCC和2例Oncocytoma进行肉眼和光镜观察、免疫组织化学染色,分析其临床病理学差异。结果 CRCC以实体结构为主、胞质半透明或嗜酸性颗粒状、核皱缩且核周有空晕;Oncocytoma以巢状结构为主,胞质嗜酸颗粒状、核圆形、核仁小。免疫组化染色显示两者均呈E-cadherin、EMA、CK20、vimentin阳性;CRCC瘤细胞CD10和CK7强阳性而S-100蛋白阴性,5名患者随访8~32个月,其中1例手术12个月后由于转移死亡;Oncocytoma瘤细胞S-100蛋白强阳性、CD10和CK7阴性,2名患者随访41个月,均未出现复发和转移。结论 CRCC和oncocytoma二者形态学各有特征,免疫表型相似,二者鉴别诊断主要在于生长方式和细胞学特征。综上所述:CRCC为惰性肿瘤,Oncocytoma为良性肿瘤,预后较好,手术切除后极少发生复发和转移。     

Renal FNA-based typing of renal masses remains a useful adjunctive modality: evaluation of 31 renal masses with correlative histology

Objectives:  Given the advances in renal imaging modalities in the recent years, a greater number of renal cell carcinomas (RCCs) with tumour size of <3 cm are being detected radiologically. Consequently, there is a pressing need for accurate typing of RCCs which, in turn, will aid in selection of cases of nephron-sparing surgery.
Methods:  A total of 31 cases of renal masses with available fine needle aspiration (FNA) material and concomitant histopathology details were retrieved. They included 27 RCCs (17 clear cells, eight papillary and two chromophobe), one oncocytoma, one liposarcoma and two benign lesions – one xanthogranulomatous pyelonephritis (XPN) and one benign cyst. Two investigators reviewed all FNA material. The degree of concordance between cytological typing and histological typing was assessed.
Results:  There was excellent agreement between the FNA typing and the final diagnosis, with correct classification in 28 of 31 cases. Among the three discordant cases, two were RCCs. The first was a papillary RCC (PRCC) that was misdiagnosed on FNA as clear cell RCC. Another case that was typed as a PRCC on final histopathology was diagnosed 'suspicious cells' on FNA. The third case was an XPN that was misdiagnosed on FNA as RCC with necrosis.
Conclusions:  There is an excellent concordance (90.3%) between the FNA diagnosis and the final histological diagnosis, especially in RCCs. There is a tendency for misdiagnosis with PRCC. Lesions with extensive necrosis and relatively insufficient diagnostic material on FNA specimens must be interpreted with caution. Better concordance might be observed with more extensive sampling.     

Preoperative diagnosis of bilateral renal oncocytoma by needle aspiration cytology. A case report

The cytohistologic and ultrastructural findings in a case of bilateral renal oncocytoma diagnosed by needle aspiration cytology are presented. This case appears to be the first reported example in which the preoperative needle aspiration cytologic diagnosis of bilateral renal oncocytoma was made due to the presence of characteristic tumor cells that were seen singly or in small clusters with rounded polygonal shapes and abundant eosinophilic granular cytoplasm. The preoperative diagnosis of bilateral oncocytoma permitted a timely decision as to the appropriate management in this case.     

肾脏原发性肿瘤CT 成像进展

肾脏原发性肿瘤种类繁多,多为恶性,且各病理亚型的影像表现均有不同。部分良性肿瘤如乏脂性血管平滑肌脂肪瘤、嗜酸细胞瘤难以与其区分,因此术前明确其组织学类型有助于治疗方案制定以及预后评估。CT是检查肾脏肿瘤的重要影像方法之一,除常规平扫、动态增强检查外,CT灌注成像、能量CT及PET-CT等亦提供了诸多信息。本文就其CT成像现状综述如下。     

Fine needle aspiration biopsy cytology of renal oncocytoma

The cytologic appearance of cells in fine needle aspiration biopsies of two cases of well-differentiated renal oncocytoma (grade 1) and one case of moderately well differentiated renal oncocytoma (grade 2) is presented. In grade 1 renal oncocytoma, the tumor cells were seen mainly singly or in small clusters; they were round or polygonal, with abundant granular and eosinophilic cytoplasm and small, regular, round, hyperchromatic nuclei. Aspirated cells from the grade 2 renal oncocytoma were seen mainly in large sheets. These cells were polygonal, with eosinophilic, granular cytoplasm and slightly irregular vesicular nuclei with prominent nucleoli.     

Immunostaining characteristics of irisin in benign and malignant renal cancers

ABSTRACT

We investigated the expression of irisin in renal cancers using immunocytochemistry. Irisin has been reported to exhibit anticancer properties. The study groups consisted of 22 cases each of control renal tissue, oncocytoma, chromophobe renal cell carcinoma (RCC), clear cell RCC (Fuhrman nuclear grades 1, 2, 3 and 4) and papillary RCC. We evaluated 10 slides for each of 176 cases. Slides were immunostained for irisin and histoscores were calculated for the prevalence and strength of immunostaining. Fuhrman nuclear grade 1, 2, 3 clear cell RCC and papillary RCC exhibited no irisin immunoreactivity. Irisin immunoreactivity was observed in some Fuhrman nuclear grade 4 RCCs. We found a significant decrease in irisin staining in chromophobe RCC compared to the control. Immunoreactivity in the oncocytoma tissue was comparable to the control group. Irisin immunoreactivity in chromophobe RCC decreased and no immunoreactivity was observed in Fuhrman nuclear grade 1, 2, 3 clear cell RCC and papillary RCC. Immunistochemical screening of irisin in renal oncocytomas and renal cancers may be useful for differential diagnosis.