Roselyne Choiniere, Shifaa' Al Qa'qa', Carol C Cheung, Antonio Finelli, Susan Prendeville
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This study aims to determine the frequency, clinicopathologic features and outcome of LOT and EVT in a single institutional series of oncocytic/eosinophilic renal neoplasms, including patients managed with active surveillance and non-surgical intervention.</p><p><strong>Methods and results: </strong>Cases were identified from a consecutive institutional series of in-house renal tumours diagnosed on biopsy and/or nephrectomy (2003-2023). Tumours with a diagnosis or differential diagnosis of oncocytoma, chromophobe renal cell carcinoma or oncocytic neoplasm not otherwise specified (including LOT, EVT and tumours with overlapping hybrid features) were retrospectively reviewed and classified/reclassified.In total, 605 oncocytic/eosinophilic renal neoplasms were reviewed, among which 33 LOT (5.5%) and 5 EVT (0.8%) were identified. LOT were CK7+, CD117- and GATA3+ (94%). EVT were CD117+, CK7 focal+ (80%) and cathepsin K+ (80%). At the median follow-up of 34 months (range 2-253) and 56 months (range 8-90) for LOT and EVT, respectively, there was no evidence of recurrence following ablation/surgical resection, metastasis or death from disease for all patients, including the 22 managed with active surveillance (20 LOT and 2 EVT).</p><p><strong>Conclusions: </strong>LOT and EVT comprised a minority of oncocytic renal neoplasms in this series. We report a large institutional series including patients managed non-surgically, with no adverse outcome, adding to the existing literature indicating a benign outcome.</p>","PeriodicalId":15391,"journal":{"name":"Journal of Clinical Pathology","volume":" ","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2024-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Frequency and clinicopathologic features of renal low-grade oncocytic tumour and eosinophilic vacuolated tumour: reclassification of 605 eosinophilic tumours including patients managed with active surveillance.\",\"authors\":\"Roselyne Choiniere, Shifaa' Al Qa'qa', Carol C Cheung, Antonio Finelli, Susan Prendeville\",\"doi\":\"10.1136/jcp-2024-209711\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>Low-grade oncocytic tumour (LOT) and eosinophilic vacuolated tumour (EVT) are recently described emerging entities, which demonstrate distinct features but are not yet recognised as separate neoplasms in the fifth WHO classification. Published series to date have been largely multi-institutional and based on surgically resected tumours. This study aims to determine the frequency, clinicopathologic features and outcome of LOT and EVT in a single institutional series of oncocytic/eosinophilic renal neoplasms, including patients managed with active surveillance and non-surgical intervention.</p><p><strong>Methods and results: </strong>Cases were identified from a consecutive institutional series of in-house renal tumours diagnosed on biopsy and/or nephrectomy (2003-2023). Tumours with a diagnosis or differential diagnosis of oncocytoma, chromophobe renal cell carcinoma or oncocytic neoplasm not otherwise specified (including LOT, EVT and tumours with overlapping hybrid features) were retrospectively reviewed and classified/reclassified.In total, 605 oncocytic/eosinophilic renal neoplasms were reviewed, among which 33 LOT (5.5%) and 5 EVT (0.8%) were identified. LOT were CK7+, CD117- and GATA3+ (94%). 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引用次数: 0
摘要
目的:低级别瘤细胞瘤(LOT)和嗜酸性空泡瘤(EVT)是最近描述的新出现的实体瘤,它们表现出不同的特征,但在第五次世界卫生组织分类中尚未被认定为单独的肿瘤。迄今为止,已发表的系列研究大多由多家机构共同完成,并以手术切除的肿瘤为基础。本研究旨在确定单一机构系列肿瘤细胞/嗜酸性粒细胞性肾肿瘤中 LOT 和 EVT 的发生频率、临床病理特征和预后,包括接受积极监测和非手术治疗的患者:病例来自连续的机构内部肾肿瘤活检和/或肾切除术诊断系列(2003-2023 年)。对诊断或鉴别诊断为肿瘤细胞瘤、嗜铬肾细胞癌或未另作说明的肿瘤细胞瘤(包括LOT、EVT和具有重叠混合特征的肿瘤)的肿瘤进行了回顾性审查和分类/再分类。共审查了605例肿瘤细胞/嗜酸性粒细胞肾肿瘤,其中发现33例LOT(5.5%)和5例EVT(0.8%)。LOT为CK7+、CD117-和GATA3+(94%)。EVT为CD117+、CK7灶+(80%)和cathepsin K+(80%)。LOT和EVT的中位随访时间分别为34个月(2-253个月)和56个月(8-90个月),所有患者均未发现消融/手术切除后复发、转移或死于疾病的证据,其中包括22名接受主动监测的患者(20名LOT患者和2名EVT患者):结论:在该系列研究中,LOT和EVT在肿瘤性肾肿瘤中占少数。我们报告了一个大型机构系列病例,其中包括非手术治疗的患者,均未出现不良后果,为现有的良性结果文献增添了新的内容。
Frequency and clinicopathologic features of renal low-grade oncocytic tumour and eosinophilic vacuolated tumour: reclassification of 605 eosinophilic tumours including patients managed with active surveillance.
Aims: Low-grade oncocytic tumour (LOT) and eosinophilic vacuolated tumour (EVT) are recently described emerging entities, which demonstrate distinct features but are not yet recognised as separate neoplasms in the fifth WHO classification. Published series to date have been largely multi-institutional and based on surgically resected tumours. This study aims to determine the frequency, clinicopathologic features and outcome of LOT and EVT in a single institutional series of oncocytic/eosinophilic renal neoplasms, including patients managed with active surveillance and non-surgical intervention.
Methods and results: Cases were identified from a consecutive institutional series of in-house renal tumours diagnosed on biopsy and/or nephrectomy (2003-2023). Tumours with a diagnosis or differential diagnosis of oncocytoma, chromophobe renal cell carcinoma or oncocytic neoplasm not otherwise specified (including LOT, EVT and tumours with overlapping hybrid features) were retrospectively reviewed and classified/reclassified.In total, 605 oncocytic/eosinophilic renal neoplasms were reviewed, among which 33 LOT (5.5%) and 5 EVT (0.8%) were identified. LOT were CK7+, CD117- and GATA3+ (94%). EVT were CD117+, CK7 focal+ (80%) and cathepsin K+ (80%). At the median follow-up of 34 months (range 2-253) and 56 months (range 8-90) for LOT and EVT, respectively, there was no evidence of recurrence following ablation/surgical resection, metastasis or death from disease for all patients, including the 22 managed with active surveillance (20 LOT and 2 EVT).
Conclusions: LOT and EVT comprised a minority of oncocytic renal neoplasms in this series. We report a large institutional series including patients managed non-surgically, with no adverse outcome, adding to the existing literature indicating a benign outcome.
期刊介绍:
Journal of Clinical Pathology is a leading international journal covering all aspects of pathology. Diagnostic and research areas covered include histopathology, virology, haematology, microbiology, cytopathology, chemical pathology, molecular pathology, forensic pathology, dermatopathology, neuropathology and immunopathology. Each issue contains Reviews, Original articles, Short reports, Correspondence and more.