首页 > 最新文献

Cytopathology最新文献

英文 中文
Does HPV-18 co-infection increase the risk of cervical pathology in individuals with HPV-16? HPV-18 合并感染是否会增加 HPV-16 感染者发生宫颈病变的风险?
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-07-11 DOI: 10.1111/cyt.13422
Mustafa Gökkaya, Aysun Alcı, Okan Aytekin, Mehmet Unsal, Caner Cakır, Okan Oktar, Necim Yalcin, Alper Kahraman, Alp Tokalioglu, Burak Ersak, Hande Esra Koca Yıldırım, Sevgi Koc, Tayfun Toptas, Fatih Kilic, Fatih Celik, Nurettin Boran, Yaprak Ustun, Ozlem Moraloglu Tekin, Gunsu Kimyon Comert, Vakkas Korkmaz, Taner Turan, Isin Ureyen

Objective

We aimed to investigate differences between HPV-16 mono- and HPV-16/18 co-infections in terms of cervical dysplasia and invasive cancer.

Methods

This multicentre, retrospective study spanned from December 2017 to December 2020, involving women who visited gynaecological oncology clinics for colposcopy with either HPV-16 or HPV-16/18 positivity. A total of 736 patients, 670 in Group 1 (HPV-16 positivity) and 66 in Group 2 (HPV-16/18 positivity), were compared for the presence of CIN2+ lesions detected by colposcopic biopsy or endocervical curettage (ECC). Exclusions included hysterectomized patients, those with prior gynaecological cancers, and patients with HPV positivity other than types 16 and 18.

Results

Among the included patients, 42.4% had a diagnosis of CIN2+ lesions. The cytology results demonstrated abnormal findings in 45.3% in Group 1 and 42.2% in Group 2, with no significant difference between the groups. ECC revealed CIN2+ lesion in 49 (8.7%) patients in group 1, while only 1 (1.7%) patient had CIN2+ lesion in group 2. There was no difference between 2 groups in terms of ECC result (p = 0.052). In group 1, 289 (43.1%) patients had CIN2+ lesion, while 23 (34.8%) patients had CIN2+ lesions in group 2. There was no difference between group 1 and 2 in terms of diagnosis of CIN2+ lesions (p = 0.19).

Conclusion

This multicentre retrospective study found no significant differences between HPV-16 mono- and HPV-16/18 co-infections regarding cervical pathologies. Larger studies are needed to validate and further explore these findings.

目的我们旨在研究HPV-16单感染和HPV-16/18合并感染在宫颈发育不良和浸润性癌症方面的差异:这项多中心回顾性研究的时间跨度为 2017 年 12 月至 2020 年 12 月,研究对象为前往妇科肿瘤诊所进行阴道镜检查的 HPV-16 或 HPV-16/18 阳性的女性。共对 736 名患者进行了比较,其中 670 人属于第 1 组(HPV-16 阳性),66 人属于第 2 组(HPV-16/18 阳性),通过阴道镜活检或宫颈内口刮宫术(ECC)检测是否存在 CIN2+ 病变。不包括子宫切除患者、曾患妇科癌症的患者以及除 16 型和 18 型以外的 HPV 阳性患者:在纳入的患者中,42.4%确诊为 CIN2+ 病变。细胞学结果显示,第 1 组和第 2 组分别有 45.3% 和 42.2% 的患者发现异常,组间差异不显著。第 1 组有 49 名(8.7%)患者的 ECC 显示病灶为 CIN2+,而第 2 组仅有 1 名(1.7%)患者的 ECC 显示病灶为 CIN2+,两组 ECC 结果无差异(P = 0.052)。第 1 组中有 289 例(43.1%)患者有 CIN2+ 病变,而第 2 组中有 23 例(34.8%)患者有 CIN2+ 病变。 第 1 组和第 2 组在 CIN2+ 病变的诊断方面没有差异(p = 0.19):这项多中心回顾性研究发现,HPV-16 单感染与 HPV-16/18 合并感染在宫颈病变方面没有明显差异。需要更大规模的研究来验证和进一步探讨这些发现。
{"title":"Does HPV-18 co-infection increase the risk of cervical pathology in individuals with HPV-16?","authors":"Mustafa Gökkaya,&nbsp;Aysun Alcı,&nbsp;Okan Aytekin,&nbsp;Mehmet Unsal,&nbsp;Caner Cakır,&nbsp;Okan Oktar,&nbsp;Necim Yalcin,&nbsp;Alper Kahraman,&nbsp;Alp Tokalioglu,&nbsp;Burak Ersak,&nbsp;Hande Esra Koca Yıldırım,&nbsp;Sevgi Koc,&nbsp;Tayfun Toptas,&nbsp;Fatih Kilic,&nbsp;Fatih Celik,&nbsp;Nurettin Boran,&nbsp;Yaprak Ustun,&nbsp;Ozlem Moraloglu Tekin,&nbsp;Gunsu Kimyon Comert,&nbsp;Vakkas Korkmaz,&nbsp;Taner Turan,&nbsp;Isin Ureyen","doi":"10.1111/cyt.13422","DOIUrl":"10.1111/cyt.13422","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>We aimed to investigate differences between HPV-16 mono- and HPV-16/18 co-infections in terms of cervical dysplasia and invasive cancer.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>This multicentre, retrospective study spanned from December 2017 to December 2020, involving women who visited gynaecological oncology clinics for colposcopy with either HPV-16 or HPV-16/18 positivity. A total of 736 patients, 670 in Group 1 (HPV-16 positivity) and 66 in Group 2 (HPV-16/18 positivity), were compared for the presence of CIN2+ lesions detected by colposcopic biopsy or endocervical curettage (ECC). Exclusions included hysterectomized patients, those with prior gynaecological cancers, and patients with HPV positivity other than types 16 and 18.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Among the included patients, 42.4% had a diagnosis of CIN2+ lesions. The cytology results demonstrated abnormal findings in 45.3% in Group 1 and 42.2% in Group 2, with no significant difference between the groups. ECC revealed CIN2+ lesion in 49 (8.7%) patients in group 1, while only 1 (1.7%) patient had CIN2+ lesion in group 2. There was no difference between 2 groups in terms of ECC result (<i>p</i> = 0.052). In group 1, 289 (43.1%) patients had CIN2+ lesion, while 23 (34.8%) patients had CIN2+ lesions in group 2. There was no difference between group 1 and 2 in terms of diagnosis of CIN2+ lesions (<i>p</i> = 0.19).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This multicentre retrospective study found no significant differences between HPV-16 mono- and HPV-16/18 co-infections regarding cervical pathologies. Larger studies are needed to validate and further explore these findings.</p>\u0000 </section>\u0000 </div>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 6","pages":"757-760"},"PeriodicalIF":1.2,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141581575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cytological features of ependymal and choroid plexus tumours 上皮和脉络丛肿瘤的细胞学特征。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-07-10 DOI: 10.1111/cyt.13418
Kristof Egervari, Ekkehard Hewer

Ependymal and choroid plexus tumours arise in anatomically related regions. Their intraoperative differential diagnosis is large and depends on factors such as age, tumour site and clinical presentation. Squash cytology can provide valuable information in this context. Cytological features of conventional ependymomas, subependymomas and myxopapillary ependymomas as well as choroid plexus tumours are reviewed and illustrated. Differential diagnostic considerations integrating morphological and clinical information are discussed.

外胚叶肿瘤和脉络丛肿瘤发生在解剖学上相关的区域。它们的术中鉴别诊断范围很广,取决于年龄、肿瘤部位和临床表现等因素。壁细胞学在这方面可以提供有价值的信息。本文回顾并阐述了传统上皮瘤、亚独立瘤、肌乳头状上皮瘤以及脉络丛肿瘤的细胞学特征。讨论了结合形态学和临床信息进行鉴别诊断的注意事项。
{"title":"Cytological features of ependymal and choroid plexus tumours","authors":"Kristof Egervari,&nbsp;Ekkehard Hewer","doi":"10.1111/cyt.13418","DOIUrl":"10.1111/cyt.13418","url":null,"abstract":"<p>Ependymal and choroid plexus tumours arise in anatomically related regions. Their intraoperative differential diagnosis is large and depends on factors such as age, tumour site and clinical presentation. Squash cytology can provide valuable information in this context. Cytological features of conventional ependymomas, subependymomas and myxopapillary ependymomas as well as choroid plexus tumours are reviewed and illustrated. Differential diagnostic considerations integrating morphological and clinical information are discussed.</p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 5","pages":"556-560"},"PeriodicalIF":1.2,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cyt.13418","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141581574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The evolving role of interventional cytopathology from thyroid FNA to NGS: Lessons learned at Federico II University of Naples. 从甲状腺 FNA 到 NGS,介入细胞病理学的作用在不断演变:那不勒斯费德里科二世大学的经验教训。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-07-09 DOI: 10.1111/cyt.13415
Elena Vigliar, Anna Maria Carillo, Mariantonia Nacchio, Domenico Cozzolino, Gennaro Acanfora, Maria Salatiello, Pasquale Pisapia, Umberto Malapelle, Giancarlo Troncone, Claudio Bellevicine

Fine-needle aspiration (FNA) guided by ultrasound (US) has emerged as a highly precise diagnostic method for managing thyroid nodules, significantly diminishing unnecessary surgeries. The effectiveness of US-guided FNA is high when a single specialist performs the FNA procedure and the microscopy. This paradigm has paved the way for the evolution of interventional cytopathology, a specialist with a pivotal role in the preoperative diagnostic process, encompassing patient history review, clinical examination, FNA execution under US guidance, preparation, and microscopic interpretation of cytological samples. As the landscape of precision medicine unfolds, molecular testing assumes greater importance in thyroid cytopathology, particularly in refining the risk of malignancy for indeterminate nodules. The updated Bethesda classification system underscores the clinical significance of molecular tests, emphasizing their role in refining diagnostic accuracy. With this evolving landscape, interventional cytopathologists must adapt by acquiring expertise in molecular technologies and addressing ongoing challenges in workflow harmonization and optimization. This paper delves into our decade-long experience as interventional cytopathologists, focusing on recent endeavours to ensure adequate samples not only for microscopic diagnosis but also for molecular testing. Additionally, here we review the challenges of integrating next-generation sequencing (NGS) technology into clinical practice, highlighting the importance of integrating clinically meaningful molecular data into comprehensive molecular cytology reports.

超声波(US)引导下的细针穿刺术(FNA)已成为治疗甲状腺结节的一种高度精确的诊断方法,大大减少了不必要的手术。如果由一名专家进行 FNA 手术和显微镜检查,那么 US 引导下 FNA 的有效性就会很高。这种模式为介入性细胞病理学的发展铺平了道路,介入性细胞病理学专家在术前诊断过程中扮演着举足轻重的角色,包括患者病史回顾、临床检查、在 US 引导下执行 FNA、准备细胞学样本并进行显微镜解读。随着精准医学的发展,分子检测在甲状腺细胞病理学中的重要性日益凸显,尤其是在细化不确定结节的恶性风险方面。更新后的贝塞斯达分类系统强调了分子检测的临床意义,强调了分子检测在提高诊断准确性方面的作用。面对不断变化的形势,介入性细胞病理学家必须掌握分子技术方面的专业知识,应对工作流程协调和优化方面的持续挑战。本文深入探讨了我们作为介入性细胞病理学家长达十年的经验,重点介绍了我们最近为确保样本不仅能用于显微诊断,还能用于分子检测所做的努力。此外,我们还回顾了将新一代测序(NGS)技术融入临床实践的挑战,强调了将具有临床意义的分子数据整合到全面的分子细胞学报告中的重要性。
{"title":"The evolving role of interventional cytopathology from thyroid FNA to NGS: Lessons learned at Federico II University of Naples.","authors":"Elena Vigliar, Anna Maria Carillo, Mariantonia Nacchio, Domenico Cozzolino, Gennaro Acanfora, Maria Salatiello, Pasquale Pisapia, Umberto Malapelle, Giancarlo Troncone, Claudio Bellevicine","doi":"10.1111/cyt.13415","DOIUrl":"https://doi.org/10.1111/cyt.13415","url":null,"abstract":"<p><p>Fine-needle aspiration (FNA) guided by ultrasound (US) has emerged as a highly precise diagnostic method for managing thyroid nodules, significantly diminishing unnecessary surgeries. The effectiveness of US-guided FNA is high when a single specialist performs the FNA procedure and the microscopy. This paradigm has paved the way for the evolution of interventional cytopathology, a specialist with a pivotal role in the preoperative diagnostic process, encompassing patient history review, clinical examination, FNA execution under US guidance, preparation, and microscopic interpretation of cytological samples. As the landscape of precision medicine unfolds, molecular testing assumes greater importance in thyroid cytopathology, particularly in refining the risk of malignancy for indeterminate nodules. The updated Bethesda classification system underscores the clinical significance of molecular tests, emphasizing their role in refining diagnostic accuracy. With this evolving landscape, interventional cytopathologists must adapt by acquiring expertise in molecular technologies and addressing ongoing challenges in workflow harmonization and optimization. This paper delves into our decade-long experience as interventional cytopathologists, focusing on recent endeavours to ensure adequate samples not only for microscopic diagnosis but also for molecular testing. Additionally, here we review the challenges of integrating next-generation sequencing (NGS) technology into clinical practice, highlighting the importance of integrating clinically meaningful molecular data into comprehensive molecular cytology reports.</p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141560420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vacuoles in a bone marrow smear: Not always reactive 骨髓涂片中的空泡:不一定有反应
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-07-09 DOI: 10.1111/cyt.13421
Karan Mayani-Mayani, Marcelo Pedro Barrios-Suvelza, Cristina Bilbao-Sieyro, Emilio González-Arnay

Vacuoles are a common observation in bone marrow smears, often related to reactive causes. The authors report a clinical case with this cytology finding in a 67-year-old male patient with systemic symptoms.

空泡是骨髓涂片中常见的现象,通常与反应性原因有关。作者报告了一个临床病例,该病例是一名 67 岁的男性患者,伴有全身症状。
{"title":"Vacuoles in a bone marrow smear: Not always reactive","authors":"Karan Mayani-Mayani,&nbsp;Marcelo Pedro Barrios-Suvelza,&nbsp;Cristina Bilbao-Sieyro,&nbsp;Emilio González-Arnay","doi":"10.1111/cyt.13421","DOIUrl":"10.1111/cyt.13421","url":null,"abstract":"<p>Vacuoles are a common observation in bone marrow smears, often related to reactive causes. The authors report a clinical case with this cytology finding in a 67-year-old male patient with systemic symptoms.</p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 5","pages":"658-660"},"PeriodicalIF":1.2,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141574947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Unleash your potential: Inside interventional pathology. 释放您的潜能:走进介入病理学。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-07-09 DOI: 10.1111/cyt.13417
Karen Villar-Zarra, Ronald Balassanian, Philippe Vielh

Interventional pathology has emerged as a pivotal force in modern healthcare, heralding a paradigm shift from traditional diagnostic approaches to patient-centered care. This innovative field bridges the gap between pathology and cytopathology, empowering pathologists to streamline diagnoses and reduce waiting times for patients. Collaborative mentorship and knowledge sharing ensure a lasting legacy of diagnostic excellence for future generations. Interventional pathology stands as a symbol of innovation and patient empowerment, offering a unified approach to diagnostics and improved care in the era of personalized medicine. This narrative chronicles the evolution of interventional pathologists from behind-the-scenes diagnostic specialists to frontline innovators. This is the story of the rise of the interventional pathologist: a testament to innovation, dedication, and an unwavering commitment to patient well-being.

介入病理学已成为现代医疗保健领域一支举足轻重的力量,预示着从传统诊断方法到以患者为中心的医疗模式的转变。这一创新领域填补了病理学与细胞病理学之间的空白,使病理学家有能力简化诊断,减少患者的等待时间。合作指导和知识共享可确保为后代留下卓越诊断的永久遗产。介入病理学是创新和患者赋权的象征,在个性化医疗时代提供了统一的诊断方法和更好的护理。本书记录了介入病理学家从幕后诊断专家到一线创新者的演变过程。这就是介入病理学家崛起的故事:创新、奉献和对患者福祉坚定不移的承诺的见证。
{"title":"Unleash your potential: Inside interventional pathology.","authors":"Karen Villar-Zarra, Ronald Balassanian, Philippe Vielh","doi":"10.1111/cyt.13417","DOIUrl":"https://doi.org/10.1111/cyt.13417","url":null,"abstract":"<p><p>Interventional pathology has emerged as a pivotal force in modern healthcare, heralding a paradigm shift from traditional diagnostic approaches to patient-centered care. This innovative field bridges the gap between pathology and cytopathology, empowering pathologists to streamline diagnoses and reduce waiting times for patients. Collaborative mentorship and knowledge sharing ensure a lasting legacy of diagnostic excellence for future generations. Interventional pathology stands as a symbol of innovation and patient empowerment, offering a unified approach to diagnostics and improved care in the era of personalized medicine. This narrative chronicles the evolution of interventional pathologists from behind-the-scenes diagnostic specialists to frontline innovators. This is the story of the rise of the interventional pathologist: a testament to innovation, dedication, and an unwavering commitment to patient well-being.</p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":" ","pages":""},"PeriodicalIF":1.2,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141560421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation and application of American College of Radiology Thyroid Imaging Reporting and Data System for improved malignancy detection in paediatric thyroid nodules 评估和应用美国放射学会甲状腺成像报告和数据系统,改进儿科甲状腺结节的恶性肿瘤检测。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-06-30 DOI: 10.1111/cyt.13414
Carlos A. Ortega, Jean-Nicolas Gallant, Irem Kilic, Siddharth Patel, Sheau-Chiann Chen, C. Burton Wood, Ryan Adams, Fadi Azer, Huiying Wang, Jiancong Liang, Sara H. Duffus, Ryan H. Belcher, Rochelle F. Andreotti, Rekha Krishnasarma, Jennifer E. Lim-Dunham, Güliz A. Barkan, Fei Ye, Vivian L. Weiss

Objective

The American College of Radiology Thyroid Imaging Reporting and Data System (TI-RADS) is a widely used method for the management of adult thyroid nodules. However, its use in paediatric patients is controversial because adult fine needle aspiration biopsy (FNAB) recommendations may lead to delayed diagnoses of cancer in children. The objectives of this study were to evaluate the performance of TI-RADS in paediatric thyroid nodules and to tailor FNAB recommendations for children.

Methods

Consecutive surgically resected paediatric thyroid nodules from two tertiary care centres between 2003 and 2021 were reviewed. Ultrasounds were blindly scored by radiologists according to TI-RADS. Management recommendations based on TI-RADS were evaluated. Various modelling methodologies were used to determine the optimal cutoff for FNAB in children.

Results

Of the 96 patients, 79 (82%) were female and the median age at surgery was 16.1 years. Fifty (52%) nodules were malignant on surgical pathology. The area under the receiver operating characteristic curve of TI-RADS for predicting malignancy was 0.78. Adult TI-RADS recommendations would have resulted in 4% of cancerous nodules being lost to follow-up. Modifications to TI-RADS (FNAB of all TR3 nodules ≥1.5 cm, FNAB of TR4 and TR5 nodules ≥0.5 cm, surveillance of nodules ≥1 cm, consider surgery for nodules >4 cm) reduced this missed malignancy rate to 0%.

Conclusions

TI-RADS can risk-stratify paediatric thyroid nodules. However, the system requires modifications to reduce the missed malignancy rate in paediatric thyroid nodules. Our data suggest that lower size thresholds for FNAB are warranted in children.

目的:美国放射学会甲状腺成像报告和数据系统(TI-RADS)是一种广泛用于成人甲状腺结节管理的方法。然而,由于成人细针穿刺活检(FNAB)建议可能导致儿童癌症诊断延迟,因此该系统在儿童患者中的应用还存在争议。本研究的目的是评估TI-RADS在儿科甲状腺结节中的表现,并为儿童量身定制FNAB建议:方法:对2003年至2021年期间在两家三级医疗中心连续手术切除的儿童甲状腺结节进行回顾性研究。放射科医生根据 TI-RADS 对超声波进行盲法评分。对基于 TI-RADS 的管理建议进行了评估。采用各种建模方法确定儿童 FNAB 的最佳临界值:在 96 名患者中,79 名(82%)为女性,手术时的中位年龄为 16.1 岁。手术病理结果显示,50 个(52%)结节为恶性。TI-RADS预测恶性的接收者操作特征曲线下面积为0.78。成人 TI-RADS 建议会导致 4% 的癌症结节失去随访机会。对 TI-RADS 的修改(对所有 TR3 结节≥1.5 厘米进行 FNAB,对 TR4 和 TR5 结节≥0.5 厘米进行 FNAB,对≥1 厘米的结节进行监测,对>4 厘米的结节考虑手术)将恶性肿瘤的漏诊率降至 0%:结论:TI-RADS 可以对儿科甲状腺结节进行风险分级。结论:TI-RADS 可以对儿科甲状腺结节进行风险分级,但需要对该系统进行修改,以降低儿科甲状腺结节的恶性漏诊率。我们的数据表明,应降低儿童 FNAB 的尺寸阈值。
{"title":"Evaluation and application of American College of Radiology Thyroid Imaging Reporting and Data System for improved malignancy detection in paediatric thyroid nodules","authors":"Carlos A. Ortega,&nbsp;Jean-Nicolas Gallant,&nbsp;Irem Kilic,&nbsp;Siddharth Patel,&nbsp;Sheau-Chiann Chen,&nbsp;C. Burton Wood,&nbsp;Ryan Adams,&nbsp;Fadi Azer,&nbsp;Huiying Wang,&nbsp;Jiancong Liang,&nbsp;Sara H. Duffus,&nbsp;Ryan H. Belcher,&nbsp;Rochelle F. Andreotti,&nbsp;Rekha Krishnasarma,&nbsp;Jennifer E. Lim-Dunham,&nbsp;Güliz A. Barkan,&nbsp;Fei Ye,&nbsp;Vivian L. Weiss","doi":"10.1111/cyt.13414","DOIUrl":"10.1111/cyt.13414","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objective</h3>\u0000 \u0000 <p>The American College of Radiology Thyroid Imaging Reporting and Data System (TI-RADS) is a widely used method for the management of adult thyroid nodules. However, its use in paediatric patients is controversial because adult fine needle aspiration biopsy (FNAB) recommendations may lead to delayed diagnoses of cancer in children. The objectives of this study were to evaluate the performance of TI-RADS in paediatric thyroid nodules and to tailor FNAB recommendations for children.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Consecutive surgically resected paediatric thyroid nodules from two tertiary care centres between 2003 and 2021 were reviewed. Ultrasounds were blindly scored by radiologists according to TI-RADS. Management recommendations based on TI-RADS were evaluated. Various modelling methodologies were used to determine the optimal cutoff for FNAB in children.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Of the 96 patients, 79 (82%) were female and the median age at surgery was 16.1 years. Fifty (52%) nodules were malignant on surgical pathology. The area under the receiver operating characteristic curve of TI-RADS for predicting malignancy was 0.78. Adult TI-RADS recommendations would have resulted in 4% of cancerous nodules being lost to follow-up. Modifications to TI-RADS (FNAB of all TR3 nodules ≥1.5 cm, FNAB of TR4 and TR5 nodules ≥0.5 cm, surveillance of nodules ≥1 cm, consider surgery for nodules &gt;4 cm) reduced this missed malignancy rate to 0%.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>TI-RADS can risk-stratify paediatric thyroid nodules. However, the system requires modifications to reduce the missed malignancy rate in paediatric thyroid nodules. Our data suggest that lower size thresholds for FNAB are warranted in children.</p>\u0000 </section>\u0000 </div>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 6","pages":"749-756"},"PeriodicalIF":1.2,"publicationDate":"2024-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/cyt.13414","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141472764","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary pulmonary epithelioid hemangioendothelioma metastatic to the pleura and mediastinal lymph node with a prominent rhabdoid cytomorphology showing CAMTA1::WWTR1 fusion and novel PRDM1 and TNFRSF14 mutations 转移至胸膜和纵隔淋巴结的原发性肺上皮样血管内皮细胞瘤,具有突出的横纹肌样细胞形态,显示CAMTA1::WWTR1融合以及新型PRDM1和TNFRSF14突变。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-06-28 DOI: 10.1111/cyt.13416
Maria F. Gonzalez, Anjali Seth

Cases of epithelioid hemangioendothelioma with WWTR1::CAMTA1 fusion can show rhabdoid cytomorphology. Lack of intracytoplasmic luminal spaces, marked rhabdoid cytomorphology, and variability in the expression of vascular markers makes the diagnosis of EHE challenging. Therefore, a high level of suspicion and ancillary studies (immunohistochemistry and next generation sequencing) help reach a definitive diagnosis in these cases.

WWTR1::CAMTA1融合的上皮样血管内皮瘤病例可表现为横纹细胞形态。由于缺乏胞浆内腔隙、明显的横纹状细胞形态以及血管标志物表达的多变性,EHE 的诊断具有挑战性。因此,高度怀疑和辅助研究(免疫组化和新一代测序)有助于对这些病例做出明确诊断。
{"title":"Primary pulmonary epithelioid hemangioendothelioma metastatic to the pleura and mediastinal lymph node with a prominent rhabdoid cytomorphology showing CAMTA1::WWTR1 fusion and novel PRDM1 and TNFRSF14 mutations","authors":"Maria F. Gonzalez,&nbsp;Anjali Seth","doi":"10.1111/cyt.13416","DOIUrl":"10.1111/cyt.13416","url":null,"abstract":"<p>Cases of epithelioid hemangioendothelioma with <i>WWTR1</i>::<i>CAMTA1</i> fusion can show rhabdoid cytomorphology. Lack of intracytoplasmic luminal spaces, marked rhabdoid cytomorphology, and variability in the expression of vascular markers makes the diagnosis of EHE challenging. Therefore, a high level of suspicion and ancillary studies (immunohistochemistry and next generation sequencing) help reach a definitive diagnosis in these cases.\u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure></p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 5","pages":"654-657"},"PeriodicalIF":1.2,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141472765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of implementing the first edition of the Paris system for reporting: A systematic review and meta-analysis 实施第一版巴黎报告制度的影响:系统回顾和荟萃分析。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-06-27 DOI: 10.1111/cyt.13407
Sahar J. Farahani, Joshua Li, Beatrice Minder, Philippe Vielh, Marija Glisic, Taulant Muka
<p>Urine cytology is a noninvasive, widely used diagnostic tool for screening and surveillance of genitourinary tract neoplasms. However, the absence of unified terminology and clear objective morphological criteria limits the clinical benefit of urine cytology. The Paris System for Reporting Urine Cytology (TPS) was developed with the goal of standardizing reporting and improving urine cytology performance in detecting high-grade malignancy (HGM). We aimed to evaluate potential effects of TPS on improving urine cytology diagnostic performance and clinical utility by conducting a systematic review and meta-analysis. We searched six electronic databases to identify cross-sectional and cohort studies written in English assessing the accuracy of urine cytology in detecting genitourinary tract malignancies of patients under surveillance or with clinical suspicion of malignancy from January 2004 to December 2022. We extracted relevant data from eligible studies to calculate relative distribution of cytology diagnostic categories; ratio of atypical to HGM cytology diagnosis; and risk of HGM (ROHGM) and HGM likelihood ratio (HGM-LR) associated with cytology diagnostic categories. We used a generalized linear mixed model with logit transformation to combine proportions and multilevel mixed-effect logistic regression to pool diagnostic accuracy measurements. We performed meta-regression to evaluate any significant difference between TPS and non-TPS cohorts. We included 64 studies for 99,796 combined total cytology samples, across 31 TPS and 49 non-TPS cohorts. Pooled relative distribution [95% confidence interval (CI)] of negative for high-grade urothelial carcinoma (NHGUC)/negative for malignancy (NM); atypical urothelial cells (AUC); suspicious for high-grade urothelial carcinoma (SHGUC)/suspicious for malignancy (SM); low-grade urothelial neoplasm (LGUN); and HGM categories among satisfactory cytology cases were 83.8% (80.3%–86.9%), 8.0% (6.0%–10.6%), 2.2% (1.4%–3.3%), 0.01% (0.0%–0.1%), and 4.2% (3.2%–5.5%) in TPS versus 80.8% (76.8–2.7%), 11.3% (8.6%–14.7%), 1.8% (1.2%–2.7%), 0.01% (0.0%–0.1%), and 3.3% (2.5%–4.3%) in non-TPS cohorts. Adopting TPS classification resulted in a significant increase in the frequency of NHGUC and a reduction in AUC cytology diagnoses, respectively. The AUC/HGM ratio in TPS cohort was 2.0, which showed a statistically significant difference from the atypical/HGM ratio of 4.1 in non-TPS cohort (<i>p</i>-value: 0.01). Moreover, the summary rate (95% CI) of LGUN called AUC on cytology significantly decreased to 20.8% (14.9%–28.3%) in the TPS compared with 34.1% (26.4%–42.8%) in non-TPS cohorts. The pooled ROHGM (95% CI) was 20.4% (6.2%–50.0%) in nondiagnostic (NDX), 15.5% (9.6%–24.2%) in NHGUC, 40.2% (30.9%–50.2%) in AUC, 80.8% (72.9%–86.8%) in SHGUC, 15.1% (5.7%–34.3%) in LGUN, and 91.4% (87.3%–94.3%) in HGM categories in TPS studies. NHGUC, AUC, SHGUC, and HGM categories were associated with HGM-LR (95% CI) of 0.2 (0.1–0.3
尿液细胞学是一种非侵入性的诊断工具,广泛用于筛查和监测泌尿生殖道肿瘤。然而,由于缺乏统一的术语和明确的客观形态学标准,限制了尿液细胞学的临床应用。巴黎尿液细胞学报告系统(TPS)的开发旨在规范尿液细胞学报告,提高尿液细胞学检测高级别恶性肿瘤(HGM)的性能。我们旨在通过进行系统回顾和荟萃分析,评估 TPS 对提高尿液细胞学诊断效果和临床实用性的潜在影响。我们检索了六个电子数据库,以确定从 2004 年 1 月到 2022 年 12 月期间评估尿液细胞学在检测受监控或临床怀疑为恶性肿瘤的患者的泌尿生殖道恶性肿瘤方面的准确性的英文横断面和队列研究。我们从符合条件的研究中提取了相关数据,以计算细胞学诊断类别的相对分布;非典型细胞学诊断与 HGM 细胞学诊断的比率;以及与细胞学诊断类别相关的 HGM 风险 (ROHGM) 和 HGM 可能性比 (HGM-LR)。我们使用了带有 logit 变换的广义线性混合模型来组合比例,并使用多层次混合效应逻辑回归来汇集诊断准确性测量结果。我们进行了元回归,以评估 TPS 和非 TPS 队列之间的显著差异。我们共纳入了 64 项研究,涉及 31 个 TPS 和 49 个非 TPS 队列中的 99,796 份合并细胞学样本。在满意的细胞学病例中,高级别尿路上皮癌阴性(NHGUC)/恶性肿瘤阴性(NM)、非典型尿路上皮细胞(AUC)、高级别尿路上皮癌可疑(SHGUC)/恶性肿瘤可疑(SM)、低级别尿路上皮肿瘤(LGUN)和HGM类别的汇总相对分布[95%置信区间(CI)]为83.8%(80.3%-86.9%)、8.0%(6.0%-10.6%)、2.2%(1.4%-3.3%)、0.01%(0.0%-0.1%)和4.2%(3.2%-5.5%)。8%(76.8%-2.7%)、11.3%(8.6%-14.7%)、1.8%(1.2%-2.7%)、0.01%(0.0%-0.1%)和 3.3%(2.5%-4.3%)。采用 TPS 分类后,NHGUC 和 AUC 细胞学诊断的频率分别显著增加和减少。TPS队列中的AUC/HGM比率为2.0,与非TPS队列中的非典型/HGM比率4.1相比,差异有统计学意义(P值:0.01)。此外,与非 TPS 队列中的 34.1%(26.4%-42.8%)相比,TPS 队列中 LGUN 在细胞学上称为 AUC 的汇总率(95% CI)显著下降至 20.8%(14.9%-28.3%)。在 TPS 研究中,汇总的 ROHGM(95% CI)在非诊断 (NDX) 中为 20.4% (6.2%-50.0%),在 NHGUC 中为 15.5% (9.6%-24.2%),在 AUC 中为 40.2% (30.9%-50.2%),在 SHGUC 中为 80.8% (72.9%-86.8%),在 LGUN 中为 15.1% (5.7%-34.3%),在 HGM 类别中为 91.4% (87.3%-94.3%)。NHGUC、AUC、SHGUC 和 HGM 类别与 HGM-LR 的相关性(95% CI)分别为 0.2(0.1-0.3)、0.9(0.6-1.3)、6.9(2.4-19.9)和 16.8(8.3-33.8)。我们的结果表明,TPS 1.0 降低了 AUC 诊断的相对频率、AUC/HGM 比率以及细胞学诊断为 AUC 的 LGUN 的频率。采用这种分类提高了 SHGUC 和 HGM 细胞学诊断在判定高级别病变时的临床实用性。然而,NHGUC 诊断并不能可靠地排除高级别病变的存在。
{"title":"Impact of implementing the first edition of the Paris system for reporting: A systematic review and meta-analysis","authors":"Sahar J. Farahani,&nbsp;Joshua Li,&nbsp;Beatrice Minder,&nbsp;Philippe Vielh,&nbsp;Marija Glisic,&nbsp;Taulant Muka","doi":"10.1111/cyt.13407","DOIUrl":"10.1111/cyt.13407","url":null,"abstract":"&lt;p&gt;Urine cytology is a noninvasive, widely used diagnostic tool for screening and surveillance of genitourinary tract neoplasms. However, the absence of unified terminology and clear objective morphological criteria limits the clinical benefit of urine cytology. The Paris System for Reporting Urine Cytology (TPS) was developed with the goal of standardizing reporting and improving urine cytology performance in detecting high-grade malignancy (HGM). We aimed to evaluate potential effects of TPS on improving urine cytology diagnostic performance and clinical utility by conducting a systematic review and meta-analysis. We searched six electronic databases to identify cross-sectional and cohort studies written in English assessing the accuracy of urine cytology in detecting genitourinary tract malignancies of patients under surveillance or with clinical suspicion of malignancy from January 2004 to December 2022. We extracted relevant data from eligible studies to calculate relative distribution of cytology diagnostic categories; ratio of atypical to HGM cytology diagnosis; and risk of HGM (ROHGM) and HGM likelihood ratio (HGM-LR) associated with cytology diagnostic categories. We used a generalized linear mixed model with logit transformation to combine proportions and multilevel mixed-effect logistic regression to pool diagnostic accuracy measurements. We performed meta-regression to evaluate any significant difference between TPS and non-TPS cohorts. We included 64 studies for 99,796 combined total cytology samples, across 31 TPS and 49 non-TPS cohorts. Pooled relative distribution [95% confidence interval (CI)] of negative for high-grade urothelial carcinoma (NHGUC)/negative for malignancy (NM); atypical urothelial cells (AUC); suspicious for high-grade urothelial carcinoma (SHGUC)/suspicious for malignancy (SM); low-grade urothelial neoplasm (LGUN); and HGM categories among satisfactory cytology cases were 83.8% (80.3%–86.9%), 8.0% (6.0%–10.6%), 2.2% (1.4%–3.3%), 0.01% (0.0%–0.1%), and 4.2% (3.2%–5.5%) in TPS versus 80.8% (76.8–2.7%), 11.3% (8.6%–14.7%), 1.8% (1.2%–2.7%), 0.01% (0.0%–0.1%), and 3.3% (2.5%–4.3%) in non-TPS cohorts. Adopting TPS classification resulted in a significant increase in the frequency of NHGUC and a reduction in AUC cytology diagnoses, respectively. The AUC/HGM ratio in TPS cohort was 2.0, which showed a statistically significant difference from the atypical/HGM ratio of 4.1 in non-TPS cohort (&lt;i&gt;p&lt;/i&gt;-value: 0.01). Moreover, the summary rate (95% CI) of LGUN called AUC on cytology significantly decreased to 20.8% (14.9%–28.3%) in the TPS compared with 34.1% (26.4%–42.8%) in non-TPS cohorts. The pooled ROHGM (95% CI) was 20.4% (6.2%–50.0%) in nondiagnostic (NDX), 15.5% (9.6%–24.2%) in NHGUC, 40.2% (30.9%–50.2%) in AUC, 80.8% (72.9%–86.8%) in SHGUC, 15.1% (5.7%–34.3%) in LGUN, and 91.4% (87.3%–94.3%) in HGM categories in TPS studies. NHGUC, AUC, SHGUC, and HGM categories were associated with HGM-LR (95% CI) of 0.2 (0.1–0.3","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 5","pages":"616-633"},"PeriodicalIF":1.2,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141460894","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Computer-assisted urine cytology: Faster, cheaper, better? 计算机辅助尿液细胞学检查:更快、更便宜、更好?
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-06-18 DOI: 10.1111/cyt.13412
Chiara Ciaparrone, Elisabetta Maffei, Vincenzo L'Imperio, Pasquale Pisapia, Catarina Eloy, Filippo Fraggetta, Pio Zeppa, Alessandro Caputo

Recent advancements in computer-assisted diagnosis (CAD) have catalysed significant progress in pathology, particularly in the realm of urine cytopathology. This review synthesizes the latest developments and challenges in CAD for diagnosing urothelial carcinomas, addressing the limitations of traditional urinary cytology. Through a literature review, we identify and analyse CAD models and algorithms developed for urine cytopathology, highlighting their methodologies and performance metrics. We discuss the potential of CAD to improve diagnostic accuracy, efficiency and patient outcomes, emphasizing its role in streamlining workflow and reducing errors. Furthermore, CAD tools have shown potential in exploring pathological conditions, uncovering novel biomarkers and prognostic/predictive features previously unknown or unseen. Finally, we examine the practical issues surrounding the integration of CAD into clinical practice, including regulatory approval, validation and training for pathologists. Despite the promising results, challenges remain, necessitating further research and validation efforts. Overall, CAD presents a transformative opportunity to revolutionize diagnostic practices in urine cytopathology, paving the way for enhanced patient care and outcomes.

计算机辅助诊断(CAD)的最新进展推动了病理学的重大进步,尤其是在尿液细胞病理学领域。本文综述了计算机辅助诊断在诊断尿路上皮癌方面的最新进展和挑战,以解决传统尿液细胞学的局限性。通过文献综述,我们确定并分析了为尿液细胞病理学开发的计算机辅助诊断模型和算法,重点介绍了它们的方法和性能指标。我们讨论了 CAD 在提高诊断准确性、效率和患者预后方面的潜力,强调了它在简化工作流程和减少错误方面的作用。此外,CAD 工具在探索病理条件、发现以前未知或未见的新型生物标记物和预后/预测特征方面也显示出了潜力。最后,我们探讨了将 CAD 纳入临床实践的实际问题,包括监管审批、验证和病理学家培训。尽管取得了令人鼓舞的成果,但挑战依然存在,需要进一步的研究和验证工作。总之,CAD 为尿液细胞病理学的诊断实践带来了变革性的机遇,为改善患者护理和治疗效果铺平了道路。
{"title":"Computer-assisted urine cytology: Faster, cheaper, better?","authors":"Chiara Ciaparrone,&nbsp;Elisabetta Maffei,&nbsp;Vincenzo L'Imperio,&nbsp;Pasquale Pisapia,&nbsp;Catarina Eloy,&nbsp;Filippo Fraggetta,&nbsp;Pio Zeppa,&nbsp;Alessandro Caputo","doi":"10.1111/cyt.13412","DOIUrl":"10.1111/cyt.13412","url":null,"abstract":"<p>Recent advancements in computer-assisted diagnosis (CAD) have catalysed significant progress in pathology, particularly in the realm of urine cytopathology. This review synthesizes the latest developments and challenges in CAD for diagnosing urothelial carcinomas, addressing the limitations of traditional urinary cytology. Through a literature review, we identify and analyse CAD models and algorithms developed for urine cytopathology, highlighting their methodologies and performance metrics. We discuss the potential of CAD to improve diagnostic accuracy, efficiency and patient outcomes, emphasizing its role in streamlining workflow and reducing errors. Furthermore, CAD tools have shown potential in exploring pathological conditions, uncovering novel biomarkers and prognostic/predictive features previously unknown or unseen. Finally, we examine the practical issues surrounding the integration of CAD into clinical practice, including regulatory approval, validation and training for pathologists. Despite the promising results, challenges remain, necessitating further research and validation efforts. Overall, CAD presents a transformative opportunity to revolutionize diagnostic practices in urine cytopathology, paving the way for enhanced patient care and outcomes.</p>","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 5","pages":"634-641"},"PeriodicalIF":1.2,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abstract 特刊:第 45 届欧洲细胞病理学大会摘要,莱比锡,2024 年 6 月 23-26 日。
IF 1.3 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-06-18 DOI: 10.1111/cyt.13404
{"title":"Abstract","authors":"","doi":"10.1111/cyt.13404","DOIUrl":"10.1111/cyt.13404","url":null,"abstract":"","PeriodicalId":55187,"journal":{"name":"Cytopathology","volume":"35 S1","pages":"5-44"},"PeriodicalIF":1.3,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141421943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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
Cytopathology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1