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Practical Approach to Reporting Based on the International System for Serous Fluid Cytopathology. 基于国际浆液细胞病理学系统的实用报告方法。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-10-02 DOI: 10.1111/cyt.13450
Eliisa Viljanen, Ivana Kholová, Ashish Chandra

The International System for Serous Fluid Cytopathology (TIS) is intended for reporting cytological specimens from serous cavities: pleural, abdominal and pericardial cavities. TIS is being adopted into practice in cytology laboratories worldwide. In this system, there are six diagnostic categories: non-diagnostic, negative for malignancy, atypia of undetermined significance, suspicious for malignancy, malignant-primary and malignant-secondary. Malignant-primary category almost always implies malignant mesothelioma and malignant-secondary usually refers to metastasis from carcinoma but also to involvement of serous cavity by haematolymphoid and other malignancies. When evaluating effusion cytological specimen adequacy, the factors that must be considered are sample volume, cellular content and cellular preservation. In the diagnostic analysis and interpretation, it is helpful to consider systematically all basic cytomorphological components in a sample. The basic components are architecture, cell populations, cell size, cytoplasm, nuclei and background elements. One important requirement for a successful evaluation of an effusion cytological specimen is sufficient clinical and radiological information in a referral. Clinical information may guide ancillary testing. In the present review, we provide a practical and educational approach to reporting serous effusion cytology based on the TIS.

国际浆液细胞病理学系统(TIS)用于报告来自浆液腔(胸膜腔、腹腔和心包腔)的细胞学标本。全世界的细胞学实验室都在采用 TIS 系统。在这一系统中,有六个诊断类别:非诊断、恶性阴性、意义不明的不典型、恶性可疑、恶性原发和恶性继发。恶性原发类几乎总是指恶性间皮瘤,恶性继发类通常指癌症转移,也指血淋巴瘤和其他恶性肿瘤累及浆腔。在评估渗出细胞学标本是否足够时,必须考虑的因素包括样本量、细胞含量和细胞保存情况。在诊断分析和解释时,系统地考虑样本中所有基本的细胞形态学成分是很有帮助的。这些基本成分包括结构、细胞群、细胞大小、细胞质、细胞核和背景元素。成功评估渗出液细胞学标本的一个重要条件是转诊时提供足够的临床和放射学信息。临床信息可为辅助检查提供指导。在本综述中,我们提供了一种基于 TIS 的实用教育方法来报告浆液性渗出细胞学。
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引用次数: 0
Metastatic Medullary Thyroid Carcinoma Presenting as an Incidental Posterior Mediastinal Mass. 转移性甲状腺髓样癌偶见纵隔后肿块
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-27 DOI: 10.1111/cyt.13449
Chaya Goldberg, DeAnna Diaz, Tamar Brandler

Medullary thyroid carcinoma (MTC) is an uncommon neuroendocrine tumour that is usually asymptomatic at its onset and therefore may not present clinically until the patient has developed advanced or metastatic disease. Common metastatic sites include cervical lymph nodes, liver, bone and lung. This is the case of a patient who presented with an incidental posterior mediastinal mass. Because the posterior mediastinum is an unusual location for MTC, MTC was not a consideration and preliminary histopathological testing did not include calcitonin, which would have been diagnostic. This case highlights the importance of testing for calcitonin more regularly when encountering a mass of unknown origin with neuroendocrine morphology, which may lead to earlier detection of MTC and thus improved prognosis.

甲状腺髓样癌(MTC)是一种不常见的神经内分泌肿瘤,发病时通常没有症状,因此可能直到患者出现晚期或转移性疾病时才会出现临床表现。常见的转移部位包括颈淋巴结、肝、骨和肺。本病例是一名偶然发现后纵隔肿块的患者。由于后纵隔是 MTC 的一个不常见部位,因此 MTC 并不在考虑之列,而且初步组织病理学检测也未包括降钙素,而降钙素本应具有诊断意义。本病例强调了在遇到来源不明的神经内分泌形态肿块时,定期检测降钙素的重要性,这可能会导致更早地发现 MTC,从而改善预后。
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引用次数: 0
Rare case of stromal predominant Wilm's tumour with rhabdomyoblastic differentiation in FNAC smears. 罕见的基质占优势的 Wilm 肿瘤病例,FNAC 涂片显示横纹肌母细胞分化。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-26 DOI: 10.1111/cyt.13445
Anjali Gupta, Radhika Srinivasan, Manish Rohilla, Nandita Kakkar, Nitin J Peters

The FNAC smear and histopathology of stromal predominant Wilm's tumour with rhabdomyoblastic Differentiation along with immunostaining in a 7-year-old male. In this paper, the diagnostic potential of FNAC in identifying rare histological variants of paediatric renal tumours is highlighted.

一名 7 岁男童的 FNAC 涂片和横纹肌细胞分化的基质占优势的 Wilm 肿瘤的组织病理学以及免疫染色。本文强调了 FNAC 在鉴别儿科肾肿瘤罕见组织学变异方面的诊断潜力。
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引用次数: 0
Adenosquamous carcinoma arising within a long-standing intrapulmonary bronchogenic cyst in an adult presenting with hyponatraemia. 一名出现低钠血症的成人肺内支气管源性囊肿中长期存在的腺鳞癌。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-23 DOI: 10.1111/cyt.13446
Adeyinka Akinsanya, Sheila Segura, Harvey Cramer, Hector Mesa

A 74-year-old woman's persistent hyponatraemia led to the discovery of an adenosquamous carcinoma within an intrapulmonary bronchogenic cyst (IPBC), diagnosed 59 years prior. This is the first reported case of such a transformation in an IPBC. An adenosquamous carcinoma, originating from an intrapulmonary bronchogenic cyst identified 59 years prior, was discovered during the workup for a patient's unexplained, persistent hyponatraemia.

一名 74 岁的妇女因持续低钠血症而在肺内支气管源性囊肿(IPBC)内发现了腺鳞癌,而该囊肿在 59 年前就已确诊。这是首例报告的 IPBC 癌变病例。在对一名不明原因的持续低钠血症患者进行检查时,发现了源自 59 年前发现的肺内支气管源性囊肿的腺鳞癌。
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引用次数: 0
Higher sensitivity of pericardial fluid cytology than biopsy in malignant effusions with potential explanation of false-negative cytology: A multi-institutional analysis. 心包积液细胞学检查对恶性渗出物的敏感性高于活组织检查,细胞学检查假阴性的可能原因:多机构分析。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-20 DOI: 10.1111/cyt.13447
Kotaro Takeda, Catherine Gereg, Xiaoying Liu, Weijie Ma, Mayara Bearse, Haiming Tang, Isabela Delfino, Eric Huang, Xiaoqi Lin, Jocelyn B Chandler, He Wang

Objective: Malignant pericardial effusions are associated with a poor prognosis. Pericardial fluid cytology and pericardial biopsy are the primary methods for diagnosis. This study aimed to conduct a multi-institutional analysis to compare the diagnostic sensitivity of cytology and biopsy, and to investigate potential explanations for false-negative results in cytology.

Methods: A retrospective review of pericardial fluid cytology cases with concurrent biopsy was conducted across four different institutions. Results were compared using standard statistical methods with attention to sensitivity and histologic distribution. False-negative cytology cases were investigated for further exploration.

Results: A total of 309 cases were collected, of which 99 (32.0%) were confirmed malignant through repeat sampling or clinical history. Pericardial fluid cytology and biopsy identified 84 and 64 malignant cases, respectively. Our findings confirmed significantly higher sensitivity of cytology compared to biopsy (84.8% vs 65.7%). The most common sites of origin were lung, breast, and gastrointestinal, with adenocarcinoma being the most prevalent histologic subtype. Histologic review of 12 false-negative cytology cases revealed three key explanations; lymphoma was the most common missed diagnosis (33.3%); fibrinous pericarditis obscures neoplastic cells on the pericardial surface; and pericardial involvement can be seen without extension into the pericardial space.

Conclusion: This study demonstrated diagnostic superiority of pericardial fluid cytology over biopsy in the evaluation of malignant pericardial effusions. We identified several limitations in fluid cytology causing false negatives. In the context of an underlying malignancy with pericardial effusion, pathologists should consider immunohistochemistry studies to aid on the diagnosis.

目的:恶性心包积液的预后较差。心包积液细胞学检查和心包活检是诊断的主要方法。本研究旨在进行多机构分析,比较细胞学和活检的诊断灵敏度,并研究细胞学假阴性结果的潜在解释:方法:四家不同机构对同时进行活检的心包积液细胞学病例进行了回顾性分析。采用标准统计方法对结果进行比较,并关注敏感性和组织学分布。对细胞学假阴性病例进行了进一步调查:结果:共收集到 309 例病例,其中 99 例(32.0%)通过重复取样或临床病史证实为恶性。心包积液细胞学检查和活组织检查分别发现了 84 例和 64 例恶性病例。我们的研究结果证实,细胞学检查的灵敏度明显高于活组织检查(84.8% 对 65.7%)。最常见的发病部位是肺、乳腺和胃肠道,腺癌是最常见的组织学亚型。对12例细胞学假阴性病例进行的组织学审查发现了三种主要解释:淋巴瘤是最常见的漏诊病例(33.3%);纤维素性心包炎掩盖了心包表面的肿瘤细胞;心包受累可在未扩展至心包间隙的情况下出现:本研究表明,在评估恶性心包积液时,心包积液细胞学诊断优于活组织检查。我们发现了体液细胞学导致假阴性的几个局限性。在潜在恶性肿瘤伴有心包积液的情况下,病理学家应考虑通过免疫组化研究来帮助诊断。
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引用次数: 0
Incidental finding in urine cytology in a patient with chronic renal disease. 一名慢性肾病患者的尿液细胞学意外发现。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-16 DOI: 10.1111/cyt.13444
Jesus Vega-Gonzalez, Montserrat de la Torre Serrano, Ana María Colino Gallardo, Antolina Rodriguez Moreno, Mª Jesús Fernández-Aceñero

An incidental finding in urine smears from a patient with a presumptive diagnosis of an IgA mesangial nephropathy is presented. A possible example of the potential value of urine cytology in functional renal disorders. We report a case of an incidental finding in urine cytology from a patient with a presumptive diagnosis of an IgA mesangial glomerulonephritis, previously diagnosed as atypical urothelial cells.

本文介绍了一名推断诊断为 IgA 系膜性肾病患者尿液涂片中的偶然发现。这是尿液细胞学在功能性肾病中的潜在价值的一个实例。我们报告了一例尿液细胞学偶然发现的病例,患者被推定诊断为IgA系膜肾小球肾炎,之前被诊断为非典型尿路上皮细胞。
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引用次数: 0
An unusual cyst at an unusual site in an adult 成人异常部位的异常囊肿
IF 1.3 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-14 DOI: 10.1111/cyt.13443
Sudha Sharma, Madhuri Dadwal, V. Anish Chandran
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引用次数: 0
Cytopathological findings of granular cell glioblastoma in intraoperative squash smear preparations: A case report 术中壁龛涂片中颗粒细胞胶质母细胞瘤的细胞病理学发现:病例报告
IF 1.3 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-13 DOI: 10.1111/cyt.13442
Samuel López‐Muñoz, Borja Sánchez‐Cordon, Mario Taravilla‐Loma, Isabel Esteban‐Rodríguez
Granular cell glioblastoma is a rare subtype of IDH‐wildtype glioblastoma, which may mimic benign macrophage‐rich brain lesions during intraoperative consultation. Few studies have previously discussed its cytopathological features with special attention to the differential diagnosis during intraoperative consultation. After a comparative analysis of previously reported cases, we found that some cytopathological findings can be useful to differentiate granular tumour cells from macrophages and other central nervous system tumours, although their presentation is not constant and clinical and radiological correlation is always critical.
颗粒细胞胶质母细胞瘤是IDH-野生型胶质母细胞瘤的一种罕见亚型,在术中会诊时可能与富含巨噬细胞的良性脑病变相似。此前很少有研究讨论其细胞病理学特征,并特别关注术中会诊时的鉴别诊断。在对以前报道的病例进行比较分析后,我们发现一些细胞病理学发现有助于将颗粒状肿瘤细胞与巨噬细胞和其他中枢神经系统肿瘤相鉴别,尽管它们的表现形式并不固定,临床和放射学相关性始终是至关重要的。
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引用次数: 0
Striated duct adenoma: The cytological description of a rare entity. 条状导管腺瘤:一种罕见病例的细胞学描述。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-09 DOI: 10.1111/cyt.13441
Montserrat De La Torre Serrano, Lorenzo Alarcón García, Ana María Colino Gallardo, Jesus Vega-Gonzalez, María Reyes Bergillos Giménez, Desiré Hernandez Martinez, Alejandro Garcia Egido, María Cruz Iglesias Moreno, Pablo Pérez-Alonso, José Carlos Plaza Hernandez, M Jesús Fernández-Aceñero

Introduction: Striated duct adenoma is a benign salivary gland tumour recently recognized by the World Health Organization. To date, no report has described the cytological features of this entity.

Materials and methods: We report the case of a 60-year-old woman with a tumour in the right parotid gland with a diameter greater than 2.4 cm confirmed by imaging tests.

Results: Two fine-needle aspiration cytologies (FNAC) were performed with inconclusive results, reporting epithelioid and spindle-shaped cellularity, with little stroma, and nuclei with abundant pseudoinclusions. Myoepithelioma and Schwannoma were proposed as differential diagnoses. An immunocytochemical panel was performed, showing positivity for S-100, SOX10, CK7 and vimentin, and negativity for both myoepithelial (p63 and calponin) and thyroid markers. In the absence of a conclusive diagnosis, the patient accepted surgery. The biopsy results confirmed diagnosis of striated duct adenoma, with immunohistochemical features superimposable to cytology.

Conclusion: Little information is available in the literature, both on biopsy and, more strikingly, on cytology of this neoplasm. The aim of this work is to provide cytological characteristics that allow diagnosis of this entity with FNAC and thus avoid unnecessary surgeries.

简介条状导管腺瘤是世界卫生组织最近确认的一种良性唾液腺肿瘤。迄今为止,还没有报告描述过这种肿瘤的细胞学特征:我们报告了一例 60 岁女性的病例,她的右侧腮腺肿瘤经影像学检查证实直径超过 2.4 厘米:结果:进行了两次细针穿刺细胞学检查(FNAC),结果均不确定,报告为上皮样和纺锤形细胞,间质少,核内有大量假包涵体。建议将肌上皮瘤和许旺瘤作为鉴别诊断。免疫细胞化学检查显示,S-100、SOX10、CK7和波形蛋白呈阳性,肌上皮(p63和钙蛋白)和甲状腺标志物呈阴性。在没有确诊的情况下,患者接受了手术治疗。活检结果确诊为横纹肌导管腺瘤,免疫组化特征与细胞学特征相叠加:结论:关于这种肿瘤的活检和细胞学方面的文献资料很少。这项工作的目的是提供细胞学特征,以便通过 FNAC 诊断这种肿瘤,从而避免不必要的手术。
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引用次数: 0
Amelanotic melanoma arising from a giant congenital melanocytic nevus - A novel entity diagnosed by fine needle aspiration. 巨型先天性黑素细胞痣引发的黑色素瘤--通过细针穿刺确诊的新病例。
IF 1.2 4区 医学 Q4 CELL BIOLOGY Pub Date : 2024-09-05 DOI: 10.1111/cyt.13439
Nandhini Gangadaran, Arunachalam Narayanan, Soundarya Ravi, Debasis Gochhait, Laxmisha Chandrashekar
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引用次数: 0
期刊
Cytopathology
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