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Carrefour Pathologie 家乐福病理科
IF 0.5 4区 医学 Q4 PATHOLOGY Pub Date : 2024-07-01 DOI: 10.1016/S0242-6498(24)00152-4
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引用次数: 0
Réseau RENAPE : vers une meilleure équité d’accès aux soins et à l’expertise pour les patients atteints de cancers rares du péritoine [RENAPE网络:让罕见腹膜癌患者更公平地获得治疗和专业知识]。
IF 0.5 4区 医学 Q4 PATHOLOGY Pub Date : 2024-07-01 DOI: 10.1016/j.annpat.2024.05.003

Crée en 2010, avec le soutien de l’Institut national du cancer et de la direction générale de l’offre de soins, le Réseau national de prise en charge des tumeurs rares du péritoine (RENAPE) s’est progressivement structuré et densifié et a permis d’optimiser les filières de soins impliquées dans le traitement des cancers rares du péritoine. Au sein du réseau, le groupe RENA-PATH s’est lui aussi développé en répondant à sa mission d’expertise diagnostique anatomopathologique, mais aussi en s’interfacant avec le groupe MESOPATH. Par ailleurs, les groupes RENAPE et RENA-PATH ont participé à la diffusion de bonnes pratiques en s’intégrant en 2019 au Thesaurus National de Cancérologie Digestive (TNCD) et en participant à de nombreux enseignements de formation post-universitaire. Cet article a pour but de rappeler de façon synthétique, les missions de RENAPE et RENA-PATH, notamment l’équité d’accès à l’expertise, et de souligner leur évolution.

Since its creation in 2010, the progressive structuration of the RENAPE network (Réseau national de prise en charge des tumeurs rares du péritoine) supported by the “Institut national du cancer” and the “Direction générale de l’offre de soins”, allowed the optimization of the healthcare system involved in the management of the rare cancers of the peritoneum. In this setting, the RENA-PATH group has also been reinforced, notably by its recognized diagnostic expertise in pathology and its interface with the MESOPATH group. Moreover RENAPE and RENA-PATH led to guidelines diffusion through the integration, in 2019, to the ``Thesaurus National de Cancérologie Digestive'' (TNCD) and to post-university medical education programs. The aim of this article is to highlight the missions of the RENAPE and RENA-PATH, notably the equity in terms of expertise, access to the networks and their improvement in the management of peritoneal diseases.

自 2010 年成立以来,在 "国家癌症研究所 "和 "医疗服务总署 "的支持下,RENAPE 网络(Réseau national de prise en charge des tumeurs rares du péritoine)逐步形成,从而优化了参与腹膜罕见癌症管理的医疗系统。在这一背景下,RENA-PATH 小组也得到了加强,特别是其在病理诊断方面的公认专长以及与 MESOPATH 小组的联系。此外,RENAPE和RENA-PATH于2019年将指南纳入 "国家消化系统癌症术语汇编"(TNCD)和大学后医学教育计划,从而促进了指南的传播。本文旨在强调RENAPE和RENA-PATH的使命,特别是在专业技术、网络访问和改善腹膜疾病管理方面的公平性。
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引用次数: 0
Histoséminaire biopsies péritonéales tumorales. Cas no 2 [腹膜肿瘤活检组织微生物学。 病例 2]。
IF 0.5 4区 医学 Q4 PATHOLOGY Pub Date : 2024-07-01 DOI: 10.1016/j.annpat.2024.06.004
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引用次数: 0
[Cutaneous adnexal tumours: Development and synthesis of diagnostic fusion genes]. [皮肤附件肿瘤:诊断性融合基因的开发与合成]。
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-06-04 DOI: 10.1016/j.annpat.2024.05.002
Thibault Kervarrec, Maxime Battistella, Nicolas Macagno

Cutaneous adnexal tumours are a heterogeneous group of epithelial lesions that includes tumours with follicular, sudoral and/or sebaceous differentiation, or even several combined lines of differentiation. Over the last few years, molecular analysis of these lesions has allowed to identify specific molecular events responsible for tumour development in an increasing number of tumour types. Like other rare neoplasms, such as soft tissue tumours, adnexal tumours display fusion genes resulting from chromosomal translocations that may be specific for the diagnosis if molecular data are properly integrated in the clinical and morphological setting. Molecular testing of adnexal tumours is valuable as it allows to strengthen the robustness of the diagnosis for a group of tumours displaying a wide morphological spectrum. It has allowed to refine the diagnostic criteria and to develop increasingly specific diagnostic immunostainings. Finally, molecular testing has been responsible for the identification of new entities or morphological subtypes of previously known entities. The aim of this review is to provide an update on cutaneous adnexal tumours associated with fusion genes and to evaluate the impact of molecular data on the diagnosis of these lesions.

皮肤附件肿瘤是一类异质性上皮病变,包括具有滤泡、窦道和/或皮脂腺分化的肿瘤,甚至是几种联合分化的肿瘤。在过去的几年中,对这些病变的分子分析已经能够确定在越来越多的肿瘤类型中导致肿瘤发生的特定分子事件。与其他罕见肿瘤(如软组织肿瘤)一样,附件肿瘤也会出现染色体易位导致的融合基因,如果能将分子数据与临床和形态学环境进行适当整合,就能对其进行特异性诊断。附件肿瘤的分子检测很有价值,因为它可以加强对一组形态谱很广的肿瘤的诊断。它有助于完善诊断标准,并开发出更具特异性的诊断免疫染色。最后,分子检测有助于确定新的实体或以前已知实体的形态亚型。本综述旨在提供与融合基因相关的皮肤附件肿瘤的最新情况,并评估分子数据对这些病变诊断的影响。
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引用次数: 0
[About a case of primary laryngeal mucosal melanoma in a patient with medical history of oropharyngeal squamous carcinoma]. [关于一例有口咽鳞癌病史的原发性喉黏膜黑色素瘤患者]。
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-06-04 DOI: 10.1016/j.annpat.2024.04.017
Alice Michaut, Guillaume Clair, Edouard Hanau, Julia Ratour, Ollivier Laccoureye, Cécile Badoual

Introduction: Primary laryngeal mucosal melanoma is a rare tumour with a poor prognosis. Its often difficult diagnosis should rule out laryngeal metastatic localization of cutaneous melanoma.

Case presentation: We report a case of primary laryngeal mucosal melanoma diagnosed in a 65-year-old man, treated 6 years previously with radio-chemotherapy and surgery for squamous cell carcinoma of the right lateral oropharyngeal region. The definitive diagnosis of primary laryngeal mucosal melanoma was made on the resection specimen, whereas the initial biopsy of the epilaryngeal mass discovered during the patient's surveillance had concluded that it was a laryngeal recurrence of the known squamous cell carcinoma.

Discussion: Through this case, we propose to remind the main characteristics and the diagnostic pitfalls of these tumours.

简介原发性喉黏膜黑色素瘤是一种罕见的肿瘤,预后较差。喉粘膜黑色素瘤的诊断通常比较困难,应排除皮肤黑色素瘤的喉转移定位:我们报告了一例原发性喉粘膜黑色素瘤病例,患者是一名 65 岁的男性,6 年前曾因右外侧口咽部位的鳞状细胞癌接受过放射化疗和手术治疗。切除标本明确诊断为原发性喉黏膜黑色素瘤,而在患者监护期间发现的会厌肿块的最初活检结论是已知鳞状细胞癌的喉部复发:通过这个病例,我们希望提醒大家这些肿瘤的主要特征和诊断误区。
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引用次数: 0
Synovialosarcome primitif du rein : si tout était déjà dans les urines pyéliques ? [肾滑膜肉瘤:如何通过肾盂细胞学进行诊断?]
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-05-01 DOI: 10.1016/j.annpat.2023.12.002
Fidélia Da Silva , Géraldine Saada-Sebag , Anne Mc Leer , Catherine Meilhac-Fournier , Séverine Valmary-Degano , Diane Giovannini

Le synovialosarcome est une tumeur mésenchymateuse maligne de l’adulte jeune, qui survient dans les tissus mous profonds, en particulier autour des grosses articulations. Lorsqu’il survient dans des sites plus inhabituels, il peut représenter alors un défi diagnostique important. Nous rapportons le cas d’une adolescente de 19 ans prise en charge pour une masse pyélique dont la cytologie urinaire pyélique faite simultanément à une biopsie pyélique s’est avérée être un élément d’orientation non négligeable et parfaitement concordant avec l’aspect histopathologique de la masse pyélique après néphrectomie. Nous rapportons ici le premier cas de synovialosarcome rénal documenté dans des urines pyéliques.

Synovialosarcoma is a malignant mesenchymal tumor of young adults that occurs in the deep soft tissues, particularly around large joints. When it occurs in more unusual sites, it could present a significant diagnostic challenge. In this case, a 19-year-old girl was treated for a pyloric mass. A pyelic urine cytology performed simultaneously with a pyloric biopsy proved to be a significant element of orientation and perfectly concordant with the histopathological aspect of the pyelic mass after nephrectomy. We report here the first case of renal synovialosarcoma documented in pyelic urine.

滑膜肉瘤是一种恶性间充质肿瘤,好发于青壮年的深部软组织,尤其是大关节周围。当它发生在较不常见的部位时,会给诊断带来很大的挑战。在本病例中,一名 19 岁的女孩因幽门肿块接受了治疗。在幽门活检的同时进行的肾盂尿液细胞学检查被证明是一个重要的定位要素,并且与肾切除术后肾盂肿块的组织病理学方面完全吻合。我们在此报告了第一例在肾盂尿液中发现的肾滑膜肉瘤。
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引用次数: 0
Un « lâcher de ballons » faussement inquiétant ! [令人震惊的 "气球释放"!]
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-05-01 DOI: 10.1016/j.annpat.2024.02.008
Arnault Tauziède-Espariat , Bertrand Grand , Ali Benali , Marie Georges , Thomas Rialland , Odette Georges
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引用次数: 0
La version 2022 du Système de Paris : quoi de neuf ? [巴黎体系,2022 年版:有什么新变化?]
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-05-01 DOI: 10.1016/j.annpat.2023.12.010
Monique Courtade-Saïdi

La deuxième version du Système de Paris pour rapporter la cytologie urinaire a été publiée en 2022. Elle fait suite à la première version de 2016 qui a connu un grand succès et été largement adoptée par de nombreux cytopathologistes de différents pays. Ainsi, de nombreuses publications utilisant le Système de Paris ont permis d’affiner les critères et d’en discuter les limites. L’accent est mis sur la pertinence de la cytologie urinaire pour la détection du carcinome urothélial de haut grade, mais pas pour celui de bas grade qui ne présente que peu d’anomalies cytologiques. Ainsi, le chapitre individualisant les néoplasmes urothéliaux de bas grade a été supprimé, ces derniers ont été inclus dans la catégorie négative pour le carcinome urothélial de haut grade. Le risque de malignité est remplacé par le risque de carcinome urothélial de haut grade, seul détectable de façon fiable en cytologie. Un nouveau chapitre a été consacré aux tumeurs urothéliales du haut appareil. Enfin, les pièges liés à la dégénérescence cellulaire sont discutés pour chacune des catégories. Le risque de carcinome urothélial de haut grade associé à chaque catégorie va faciliter la communication avec le clinicien et la prise en charge des patients.

The second version of the Paris System for reporting urine cytology was published in 2022. It follows the first version of 2016, which was very successful and widely adopted by many cytopathologists from different countries. Thus, numerous publications using the Paris System have made possible to refine the criteria as well as discussing the limits. The diagnostic accuracy of urinary cytology is high for detection of high-grade urothelial carcinoma, but not for low-grade carcinoma where there are few cytological abnormalities. So, the chapter individualizing low-grade urothelial neoplasms was deleted; the latter were included in the category “negative for high-grade urothelial carcinoma”. Indeed, the risk of malignancy is replaced by the risk of high-grade urothelial carcinoma. A new chapter has been devoted to urothelial tumors of the upper tract. Finally, the pitfalls linked to cellular degeneration are discussed for each category. The risk of high-grade malignancy associated with each category will help communication with the clinician and help patient care.

用于尿液细胞学报告的巴黎系统第二版于 2022 年发布。这是继 2016 年第一版之后的又一版本,第一版非常成功,被不同国家的许多细胞病理学家广泛采用。因此,大量使用巴黎体系的出版物使得对标准的完善和限制的讨论成为可能。尿液细胞学在检测高级别尿路上皮癌方面具有很高的诊断准确性,但对于细胞学异常较少的低级别癌,诊断准确性则不高。因此,删除了关于低级别尿路上皮肿瘤的章节;后者被列入 "高级别尿路上皮癌阴性 "类别。事实上,恶性肿瘤的风险被高级别尿路上皮癌的风险所取代。新的一章专门讨论上尿路的尿路上皮肿瘤。最后,讨论了每一类肿瘤与细胞变性有关的隐患。与每个类别相关的高级别恶性肿瘤风险将有助于与临床医生的沟通,并有助于患者护理。
{"title":"La version 2022 du Système de Paris : quoi de neuf ?","authors":"Monique Courtade-Saïdi","doi":"10.1016/j.annpat.2023.12.010","DOIUrl":"10.1016/j.annpat.2023.12.010","url":null,"abstract":"<div><p>La deuxième version du Système de Paris pour rapporter la cytologie urinaire a été publiée en 2022. Elle fait suite à la première version de 2016 qui a connu un grand succès et été largement adoptée par de nombreux cytopathologistes de différents pays. Ainsi, de nombreuses publications utilisant le Système de Paris ont permis d’affiner les critères et d’en discuter les limites. L’accent est mis sur la pertinence de la cytologie urinaire pour la détection du carcinome urothélial de haut grade, mais pas pour celui de bas grade qui ne présente que peu d’anomalies cytologiques. Ainsi, le chapitre individualisant les néoplasmes urothéliaux de bas grade a été supprimé, ces derniers ont été inclus dans la catégorie négative pour le carcinome urothélial de haut grade. Le risque de malignité est remplacé par le risque de carcinome urothélial de haut grade, seul détectable de façon fiable en cytologie. Un nouveau chapitre a été consacré aux tumeurs urothéliales du haut appareil. Enfin, les pièges liés à la dégénérescence cellulaire sont discutés pour chacune des catégories. Le risque de carcinome urothélial de haut grade associé à chaque catégorie va faciliter la communication avec le clinicien et la prise en charge des patients.</p></div><div><p>The second version of the Paris System for reporting urine cytology was published in 2022. It follows the first version of 2016, which was very successful and widely adopted by many cytopathologists from different countries. Thus, numerous publications using the Paris System have made possible to refine the criteria as well as discussing the limits. The diagnostic accuracy of urinary cytology is high for detection of high-grade urothelial carcinoma, but not for low-grade carcinoma where there are few cytological abnormalities. So, the chapter individualizing low-grade urothelial neoplasms was deleted; the latter were included in the category “negative for high-grade urothelial carcinoma”. Indeed, the risk of malignancy is replaced by the risk of high-grade urothelial carcinoma. A new chapter has been devoted to urothelial tumors of the upper tract. Finally, the pitfalls linked to cellular degeneration are discussed for each category. The risk of high-grade malignancy associated with each category will help communication with the clinician and help patient care.</p></div>","PeriodicalId":50969,"journal":{"name":"Annales De Pathologie","volume":"44 3","pages":"Pages 188-194"},"PeriodicalIF":0.5,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139503108","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
Revue de presse [文献集锦]。
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-05-01 DOI: 10.1016/j.annpat.2024.04.002
Audrey Rousseau
{"title":"Revue de presse","authors":"Audrey Rousseau","doi":"10.1016/j.annpat.2024.04.002","DOIUrl":"10.1016/j.annpat.2024.04.002","url":null,"abstract":"","PeriodicalId":50969,"journal":{"name":"Annales De Pathologie","volume":"44 3","pages":"Pages 156-158"},"PeriodicalIF":0.5,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140760424","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
Un carcinome basocellulaire avec différenciation myoépithéliale [基底细胞癌伴有肌上皮分化]。
IF 0.5 4区 医学 Q4 Medicine Pub Date : 2024-05-01 DOI: 10.1016/j.annpat.2024.02.004
Claire David, Antoine Taillandier, Paul-Louis Chantreau, Rémy Kerdraon, Flore Delalande, Patrick Michenet
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引用次数: 0
期刊
Annales De Pathologie
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