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Journal of the American Society of Cytopathology最新文献

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Optimal utilization of paucicellular vitreous sample for diagnosis of primary vitreoretinal lymphoma 玻璃体少细胞标本在原发性玻璃体视网膜淋巴瘤诊断中的最佳应用。
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.05.006
Armughan S. Khan MBBS, Anam Khan MD, Zarrin Hossein-Zadeh MD, Lawra Murray CT, MS (ASCP), Karen Chau MBA, CT(ASCP), Atif Khan MD, Xinmin Zhang MD, Rubina S. Cocker MD

Introduction

Primary vitreoretinal lymphoma (PVRL) is a rare, aggressive, and intraocular non-Hodgkin lymphoma, typically manifesting as diffuse large B-cell lymphoma (95%). Vitreous fluid cytology is the gold standard for diagnosis; however, its utility is limited by poor preservation and low cellularity. Recent studies indicate that myeloid differentation primary response protein 88 (MYD88) mutation analysis is more sensitive and accurate on low-cellularity or poorly preserved samples. The incidence of PVRL has reportedly tripled with an annual average of ∼50 cases in the United States. Delayed diagnosis can lead to mortality within 2 years, underscoring the need for improved diagnostic methods.

Materials and methods

We conducted a 5-year retrospective study of vitreous samples from 3 tertiary centers. A cytopathologist and a hematopathologist reviewed the samples and classified them as “negative,” “atypical,” or “positive.” Whole slide imaging (WSI) was incorporated to quantify atypical lymphocytes using an arbitrary cutoff (≥25% considered positive; <25% considered atypical) and to document necrosis and apoptosis. Ancillary tests included flow cytometry, immunohistochemistry (IHC), and MYD88 mutation analysis.

Results

Of the 226 samples, 214 were diagnosed as negative, 6 as atypical, and 6 as positive. WSI enhanced the diagnosis by precisely quantifying atypical lymphocytes. Flow cytometry was conclusive in 2 of 8 cases, IHC in 7 of 8, and MYD88 analysis in 4 of 5 cases.

Conclusions

While cytology remains the gold standard, a combination of WSI, targeted IHC, and MYD88 analysis enhances diagnostic precision in paucicellular samples. Flow cytometry should be reserved for cases with high cellularity and strong clinical suspicion.
原发性玻璃体视网膜淋巴瘤(PVRL)是一种罕见的侵袭性眼内非霍奇金淋巴瘤,典型表现为弥漫性大b细胞淋巴瘤(95%)。玻璃体细胞学是诊断的金标准;然而,由于保存不良和细胞密度低,其应用受到限制。最近的研究表明,髓样分化初级反应蛋白88 (MYD88)突变分析在低细胞或保存不良的样品中更为敏感和准确。据报道,在美国,PVRL的发病率增加了三倍,平均每年增加50例。延迟诊断可导致2年内死亡,这强调了改进诊断方法的必要性。材料和方法:我们对3个三级中心的玻璃体样本进行了为期5年的回顾性研究。一名细胞病理学家和一名血液病理学家检查了这些样本,并将它们分为“阴性”、“非典型”和“阳性”。采用全切片成像(WSI)定量非典型淋巴细胞,采用任意截止(≥25%认为阳性;结果:226例标本中,阴性214例,不典型6例,阳性6例。WSI通过精确定量非典型淋巴细胞来提高诊断。8例中有2例流式细胞术结论性,8例中有7例免疫组化,5例中有4例MYD88分析。结论:虽然细胞学仍然是金标准,但WSI、靶向免疫组化和MYD88分析的结合提高了对少细胞样本的诊断精度。流式细胞术应保留在高细胞和临床怀疑强的病例。
{"title":"Optimal utilization of paucicellular vitreous sample for diagnosis of primary vitreoretinal lymphoma","authors":"Armughan S. Khan MBBS,&nbsp;Anam Khan MD,&nbsp;Zarrin Hossein-Zadeh MD,&nbsp;Lawra Murray CT, MS (ASCP),&nbsp;Karen Chau MBA, CT(ASCP),&nbsp;Atif Khan MD,&nbsp;Xinmin Zhang MD,&nbsp;Rubina S. Cocker MD","doi":"10.1016/j.jasc.2025.05.006","DOIUrl":"10.1016/j.jasc.2025.05.006","url":null,"abstract":"<div><h3>Introduction</h3><div>Primary vitreoretinal lymphoma (PVRL) is a rare, aggressive, and intraocular non-Hodgkin lymphoma, typically manifesting as diffuse large B-cell lymphoma (95%). Vitreous fluid cytology is the gold standard for diagnosis; however, its utility is limited by poor preservation and low cellularity. Recent studies indicate that myeloid differentation primary response protein 88 (MYD88) mutation analysis is more sensitive and accurate on low-cellularity or poorly preserved samples. The incidence of PVRL has reportedly tripled with an annual average of ∼50 cases in the United States. Delayed diagnosis can lead to mortality within 2 years, underscoring the need for improved diagnostic methods.</div></div><div><h3>Materials and methods</h3><div>We conducted a 5-year retrospective study of vitreous samples from 3 tertiary centers. A cytopathologist and a hematopathologist reviewed the samples and classified them as “negative,” “atypical,” or “positive.” Whole slide imaging (WSI) was incorporated to quantify atypical lymphocytes using an arbitrary cutoff (≥25% considered positive; &lt;25% considered atypical) and to document necrosis and apoptosis<span>. Ancillary tests included flow cytometry, immunohistochemistry (IHC), and MYD88 mutation analysis.</span></div></div><div><h3>Results</h3><div>Of the 226 samples, 214 were diagnosed as negative, 6 as atypical, and 6 as positive. WSI enhanced the diagnosis by precisely quantifying atypical lymphocytes. Flow cytometry was conclusive in 2 of 8 cases, IHC in 7 of 8, and MYD88 analysis in 4 of 5 cases.</div></div><div><h3>Conclusions</h3><div>While cytology remains the gold standard, a combination of WSI, targeted IHC, and MYD88 analysis enhances diagnostic precision in paucicellular samples. Flow cytometry should be reserved for cases with high cellularity and strong clinical suspicion.</div></div>","PeriodicalId":38262,"journal":{"name":"Journal of the American Society of Cytopathology","volume":"14 5","pages":"Pages 317-326"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144498275","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimizing cytology and small biopsy specimen processing for ancillary studies: recommendations from the American Society of Cytopathology taskforce 优化辅助研究的细胞学和小活检标本处理:来自美国细胞病理学会工作组的建议。
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.06.002
Sinchita Roy-Chowdhuri MD, PhD , Christine N. Booth MD , Jonas J. Heymann MD , Elizabeth Jenkins MS , Joshua R. Menke MD , Sara E. Monaco MD , Ritu Nayar MD , Michiya Nishino MD, PhD , Roberto Ruiz-Cordero MD , Donna K. Russell MEd, CT (ASCP) , Anjali Saqi MD, MBA , Kaitlin E. Sundling MD, PhD , Michael J. Thrall MD , Vanda F. Torous MD , Christopher J. VandenBussche MD, PhD , M. Lisa Zhang MD , Momin T. Siddiqui MD , Paul A. VanderLaan MD, PhD

Introduction

Clinically acquired cytopathology and small biopsy specimens provide essential diagnostic and predictive biomarker information that underlies precision medicine and patient care decisions. Biomarker testing using immunochemistry, in situ hybridization, and molecular analysis is routinely used to inform therapeutic decisions and monitor therapy. Cytopathology and small biopsy specimen collection, handling, and processing vary across different practices and are frequently determined by individual laboratory preference. Thus, clinical specimens are subject to different preanalytical variables that can impact downstream nucleic acid quality and protein antigenicity, compromising the reliability of the ancillary testing results.

Materials and methods

Based on a recent survey by the American Society of Cytopathology there is wide variation in current practices for specimen collection and processing, reflecting a lack of consensus and standardization among cytopathology laboratories. To address this need, the American Society of Cytopathology established a special task force comprising 18 members with expertise and/or interest in ancillary studies in cytopathology and small biopsy specimens.

Results

The task force conducted a survey of existing practices in cytopathology laboratories. A scoping review was performed to identify published literature for relevant evidence focusing on specific areas of interest. The existing literature on preanalytical variables in small specimens and their impact on ancillary studies were reviewed and data were compiled to draft best practice recommendations.

Conclusions

The task force has developed these evidence-based best practice recommendations for optimizing and standardizing preanalytical variables in small specimens to ensure quality and reliability of ancillary studies.
临床获得的细胞病理学和小活检标本提供必要的诊断和预测性生物标志物信息,是精准医学和患者护理决策的基础。使用免疫化学、原位杂交和分子分析的生物标志物检测通常用于告知治疗决策和监测治疗。细胞病理学和小活检标本的收集、处理和处理在不同的实践中有所不同,通常由个人实验室偏好决定。因此,临床标本受到不同的分析前变量的影响,这些变量会影响下游核酸质量和蛋白质抗原性,从而影响辅助检测结果的可靠性。材料和方法:根据美国细胞病理学学会最近的一项调查,目前标本收集和处理的实践存在很大差异,反映了细胞病理学实验室之间缺乏共识和标准化。为了满足这一需求,美国细胞病理学学会成立了一个特别工作组,由18名成员组成,他们在细胞病理学和小活检标本的辅助研究方面具有专业知识和/或兴趣。材料和方法:工作组对细胞病理学实验室的现有做法进行了调查。进行范围审查,以确定已发表的文献的相关证据,重点关注特定领域的兴趣。现有的小样本分析前变量及其对辅助研究的影响的文献进行了审查和数据汇编,以起草最佳实践建议。结论:工作组已经制定了这些基于证据的最佳实践建议,以优化和标准化小样本分析前变量,以确保辅助研究的质量和可靠性。
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引用次数: 0
Anal Cytology and High-Risk HPV Cotesting: Clinical Features and Histologic Correlation 肛门细胞学和高危HPV检测:临床特征和组织学相关性
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.073
Bilge Dundar MD, Yi Zhu MD, PhD, Chuan Chen MD, PhD, Meredith VandeHaar SCT(ASCP), Kristina Lewis CT(ASCP), Erin Ulrich SCT(ASCP), Amy Swanson MD, Diva Salomao MD, Yajue Huang MD, PhD
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引用次数: 0
Diagnostic Utility of Touch Imprint Cytology of Core Needle Biopsy of Lung Masses: A Comparative Analysis of CT-Guided Versus Endobronchial Ultrasound-Guided Lung Core Needle Biopsies 触摸印迹细胞学对肺肿块核心穿刺活检的诊断价值:ct引导与支气管超声引导下肺核心穿刺活检的比较分析
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.045
Shilpa Reddy DO, Kamal Khurana MD, Cindy A. Steele SCT(ASCP), Patrick Fasulo BS, CT(ASCP)
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引用次数: 0
Seven-Year Institutional Experience in Subtyping of Salivary Gland Neoplasm of Uncertain Malignant Potential 七年机构经验涎腺肿瘤的亚型不确定恶性潜能
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.040
Niraj Vyas MD, MBS, Juan Xing MD
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引用次数: 0
Prospective Multi-Reader Study for Evaluating the Feasibility of Whole Slide Imaging for Rapid Onsite Evaluation of Thyroid Fine Needle Aspiration 评估全切片成像用于甲状腺细针穿刺快速现场评估可行性的前瞻性多读卡器研究
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.026
Mohammed Ahmed MD, Dianna Almaraz-Klippel MS, Gloria Sura MD, Uma Kundu MD, Wendong Yu MD, PhD, John Stewart MD, PhD, Qiong Gan MD, Savitri Krishnamurthy MD
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引用次数: 0
Temporal Trends of Abnormal Cervical Cytology in an Underserved Free Clinic Population: A Six-Year Experience 在服务不足的免费诊所人群中异常宫颈细胞学的时间趋势:六年的经验
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.068
Sean Byrne DO, Jason Willis CT(ASCP), MBA, Mohamad Gafeer MD, Swati Satturwar MD, Hamza Gokozan MD
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引用次数: 0
WHO Reporting System for Pancreaticobiliary Cytopathology: Correlation with Malignancy and Survival WHO胰胆管细胞病理学报告系统:与恶性肿瘤和生存的关系
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.017
Nadwa Bustami MD, Christopher Moroz MD, Vijayalakshmi Padmanabhan MBBS, MD, MPH
{"title":"WHO Reporting System for Pancreaticobiliary Cytopathology: Correlation with Malignancy and Survival","authors":"Nadwa Bustami MD,&nbsp;Christopher Moroz MD,&nbsp;Vijayalakshmi Padmanabhan MBBS, MD, MPH","doi":"10.1016/j.jasc.2025.07.017","DOIUrl":"10.1016/j.jasc.2025.07.017","url":null,"abstract":"","PeriodicalId":38262,"journal":{"name":"Journal of the American Society of Cytopathology","volume":"14 5","pages":"Pages S15-S16"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145100043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cytologic, Clinicopathologic and Radiologic Findings of Pancreatic Solitary Fibrous Tumor: Our Institutional Experience 胰腺孤立性纤维性肿瘤的细胞学、临床病理和影像学表现:我们的机构经验
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.018
Kelsey McHugh MD , Maria Luisa Policarpio-Nicolas MD
{"title":"Cytologic, Clinicopathologic and Radiologic Findings of Pancreatic Solitary Fibrous Tumor: Our Institutional Experience","authors":"Kelsey McHugh MD ,&nbsp;Maria Luisa Policarpio-Nicolas MD","doi":"10.1016/j.jasc.2025.07.018","DOIUrl":"10.1016/j.jasc.2025.07.018","url":null,"abstract":"","PeriodicalId":38262,"journal":{"name":"Journal of the American Society of Cytopathology","volume":"14 5","pages":"Page S16"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145100044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Follow-Up Outcomes of High Grade Squamous Intraepithelial Lesion (HSIL) Cytology with High-Risk Human Papillomavirus (HR HPV) Genotypes Other Than 16/18 16/18以外高危人乳头瘤病毒(HR HPV)基因型的高级别鳞状上皮内病变(HSIL)细胞学随访结果
Q2 Medicine Pub Date : 2025-09-01 DOI: 10.1016/j.jasc.2025.07.061
Patrick Bladek MD, Kristen Bevans-Wilkins DHSc, MBA, SCT(ASCP), Julian Tan DO, Robert Cabay MD, DDS, Odile David MD
{"title":"Follow-Up Outcomes of High Grade Squamous Intraepithelial Lesion (HSIL) Cytology with High-Risk Human Papillomavirus (HR HPV) Genotypes Other Than 16/18","authors":"Patrick Bladek MD,&nbsp;Kristen Bevans-Wilkins DHSc, MBA, SCT(ASCP),&nbsp;Julian Tan DO,&nbsp;Robert Cabay MD, DDS,&nbsp;Odile David MD","doi":"10.1016/j.jasc.2025.07.061","DOIUrl":"10.1016/j.jasc.2025.07.061","url":null,"abstract":"","PeriodicalId":38262,"journal":{"name":"Journal of the American Society of Cytopathology","volume":"14 5","pages":"Page S39"},"PeriodicalIF":0.0,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145100057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of the American Society of Cytopathology
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