Annales de biologie clinique最新文献

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Poor-prognosis histoplasmosis: a crystal blue-green persuasion. 预后不良的组织胞浆菌病:蓝绿色的水晶劝说。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1914
Fatma Smaoui, Ibrahima Faye, Olivier Moquet
{"title":"Poor-prognosis histoplasmosis: a crystal blue-green persuasion.","authors":"Fatma Smaoui, Ibrahima Faye, Olivier Moquet","doi":"10.1684/abc.2024.1914","DOIUrl":"10.1684/abc.2024.1914","url":null,"abstract":"","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"479-480"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142367839","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
[Epidemiology of urolithiasis in south of Tunisia]. [突尼斯南部的尿石症流行病学]。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1902
Khouloud Mzid, Aida Elleuch, Dana Jallouli, Khansa Chaabouni, Mouna Turki, Fatma Makni Ayadi
{"title":"[Epidemiology of urolithiasis in south of Tunisia].","authors":"Khouloud Mzid, Aida Elleuch, Dana Jallouli, Khansa Chaabouni, Mouna Turki, Fatma Makni Ayadi","doi":"10.1684/abc.2024.1902","DOIUrl":"10.1684/abc.2024.1902","url":null,"abstract":"<p><p>Determine the epidemiological characteristics of urolithiasis in the South region of Tunisia and the impact of age and sex on stone composition. We conducted a retrospective study including patient records whose urinary lithiasis was analyzed within the biochemistry department of CHU Habib Bourguiba of Sfax (2011-2020). Stone analysis was performed using a stereomicroscope and infrared spectroscopy. A total of 1127 stones were analyzed. The sex ratio was 2,6. Renal Colic pain was the most common symptom (48,3%). The most frequent localization of the stones (84.6%) was the upper urinary tract. Whewellite was the most common component (64.1%). The study of stone component according to age showed a decrease in the frequency of weddellite (p = 0,024) and an increase in the frequency of uric acid stones with age (p < 0,001). Whewellite was more frequent in men (p = 0.022) and, notably in our series, uric acid was significantly more frequent in women (p < 0.001). The epidemiological profile of urolithiasis in south of Tunisia is similar to that observed in industrialized countries.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"376-386"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115841","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
[Evaluation of a semi-automated test for quantification of von Willebrand multimers]. [评估用于量化 von Willebrand 多聚物的半自动化检验]。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1903
Christophe Peronino, Nadia Rivet, Nathalie Itzhar-Baikian, Aurélien Philippe, Bérangère S Joly, Joseph Roux de Bezieux, Anne-Céline Martin, Sophie Luneau, Agnès Veyradier, Pascale Gaussem, Nicolas Gendron, David M Smadja
{"title":"[Evaluation of a semi-automated test for quantification of von Willebrand multimers].","authors":"Christophe Peronino, Nadia Rivet, Nathalie Itzhar-Baikian, Aurélien Philippe, Bérangère S Joly, Joseph Roux de Bezieux, Anne-Céline Martin, Sophie Luneau, Agnès Veyradier, Pascale Gaussem, Nicolas Gendron, David M Smadja","doi":"10.1684/abc.2024.1903","DOIUrl":"10.1684/abc.2024.1903","url":null,"abstract":"<p><p>The assessment of von Willebrand factor (VWF) multimer distribution, particularly following the implantation of circulatory support devices, is a crucial parameter in hemostasis. Our study aimed to evaluate the semi-automated quantification of VWF multimers using the Sebia Hydrasys analyzer. Our analysis focused on quantifying high molecular weight, intermediate weight, and low molecular weight VWF multimers. Electrophoretic migration was performed using the Hydrasys 2 scan, and interpretation was carried out using densitometric analysis with the Phoresis software. The Hydrasys scan 2 successfully separated all the expected VWF multimer profiles based on the type of von Willebrand disease. The analysis revealed that in patients with circulatory support devices, elevated levels of plasma VWF rendered multimer migration unanalyzable using the methodology recommended by the manufacturer. Therefore, adjustment to a 100 % VWF antigenic level improved gel precision. We also suggest using as a standardized control the Cryocheck™ plasma, and have established reference values. Overall, this semi-automated, standardized, and optimized VWF multimer analysis system allows for an effective assessment of the VWF multimeric profile.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"361-375"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115842","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
Identification of susceptibility modules and characteristic genes to osteoarthritis by WGCNA. 通过 WGCNA 鉴定骨关节炎的易感性模块和特征基因。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1913
He-Jun Hu, Chao Kuang, Ru-Lin Deng, Zhi-Jun Zheng, Kang-Yan Liu, Xing-Xing Wei
{"title":"Identification of susceptibility modules and characteristic genes to osteoarthritis by WGCNA.","authors":"He-Jun Hu, Chao Kuang, Ru-Lin Deng, Zhi-Jun Zheng, Kang-Yan Liu, Xing-Xing Wei","doi":"10.1684/abc.2024.1913","DOIUrl":"10.1684/abc.2024.1913","url":null,"abstract":"<p><p>The susceptibility modules and characteristic genes of patients with osteoarthritis (OA) were determined by weighted gene co-expression network analysis (WGCNA), and the role of immune cells in OA related microenvironment was analyzed. GSE98918 and GSE117999 data sets are from GEO database. R language was used to conduct difference analysis for the new data set after merging. The formation of gene co-expression network, screening of susceptibility modules and screening of core genes are all through WGCNA. GO and KEGG enrichment analyses were used for Hub genes. The characteristic genes of the disease were obtained by Lasso regression screening. SSGSEA was used to estimate immune cell abundance in sample and a series of correlation analyses were performed. WGCNA was used to form 6 gene co-expression modules. The yellow-green module is identified as the susceptible module of OA. 202 genes were identified as core genes. Finally, RHOT2, FNBP4 and NARF were identified as the characteristic genes of OA. The results showed that the characteristic genes of OA were positively correlated with plasmacytoid dendritic cells, NKT cells and immature dendritic cells, but negatively correlated with active B cells. MDSC were the most abundant immune cells in cartilage. This study identified the Hippo signaling pathway, mTOR signaling pathway, and three characteristic genes (RHOT2, FNBP4, NARF) as being associated with osteoarthritis (OA). These three genes are downregulated in the cartilage of OA patients and may serve as biomarkers for early diagnosis and targeted therapy. Proper regulation of immune cells may aid in the treatment of OA. Future research should focus on developing tools to detect these genes and exploring their therapeutic applications.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"423-437"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142303181","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
Clinical values of MRSI, CRP and FABP4 in the diagnosis and prognosis of acute pancreatitis. MRSI、CRP 和 FABP4 在急性胰腺炎诊断和预后中的临床价值。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1909
Xi Wu, Ziqiang Guo, Ming Yu, Yunge Wu
{"title":"Clinical values of MRSI, CRP and FABP4 in the diagnosis and prognosis of acute pancreatitis.","authors":"Xi Wu, Ziqiang Guo, Ming Yu, Yunge Wu","doi":"10.1684/abc.2024.1909","DOIUrl":"10.1684/abc.2024.1909","url":null,"abstract":"<p><p>To examine the clinical values of C-reactive protein (CRP), fatty acid-binding protein 4 (FABP4) and magnetic resonance severity index (MRSI) in acute pancreatitis (AP) cases. 70 AP patients and another 70 healthy controls were recruited, and the MRSI score was calculated. Receiver operator characteristic (ROC) curve was used for diagnostic performance analysis. FABP4 levels were elevated in AP patients, and significantly correlated with CRP and MRSI score. Serum FABP4 and MRSI score displayed high diagnostic performance for AP. FABP4, MRSI score and CRP levels were positively correlated with disease severity. MRSI score and FABP4 were independently related to patients' survival, and showed high predictive values. FABP4 may serve as a potential marker for the diagnosis of AP, with the advantages of low cost and high simplicity. The levels of FABP4 and MRSI score can predict the poor survival of the patients.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"413-422"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115848","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
[Quand la leucémie à tricholeucocytes rencontre la légionellose]. [当毛细胞白血病遇上军团病]。
Annales de biologie clinique Pub Date : 2024-09-19 DOI: 10.1684/abc.2024.1906
Ludovic Bergon, Brigitte Riviere, Pauline Condom, Jean-Baptiste Rieu
{"title":"[Quand la leucémie à tricholeucocytes rencontre la légionellose].","authors":"Ludovic Bergon, Brigitte Riviere, Pauline Condom, Jean-Baptiste Rieu","doi":"10.1684/abc.2024.1906","DOIUrl":"10.1684/abc.2024.1906","url":null,"abstract":"","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 4","pages":"475-477"},"PeriodicalIF":0.0,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115846","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
[Acquired hemophilia A and emicizumab for the treatment of bleeding: two case report and a literature review]. [获得性血友病 A 与治疗出血的埃米珠单抗:两例病例报告和文献综述]。
Annales de biologie clinique Pub Date : 2024-08-30 DOI: 10.1684/abc.2024.1900
Amélie Launois, Isabelle Martin-Toutain, Floriane Devaux, Juliette Lambert, Thomas Longval, Fatiha Merabet, Rym Jaidi, Sophie Le Dore, Emmanuelle Ferre, Philippe Rousselot, Emmanuelle De Raucourt, Claire Flaujac
{"title":"[Acquired hemophilia A and emicizumab for the treatment of bleeding: two case report and a literature review].","authors":"Amélie Launois, Isabelle Martin-Toutain, Floriane Devaux, Juliette Lambert, Thomas Longval, Fatiha Merabet, Rym Jaidi, Sophie Le Dore, Emmanuelle Ferre, Philippe Rousselot, Emmanuelle De Raucourt, Claire Flaujac","doi":"10.1684/abc.2024.1900","DOIUrl":"10.1684/abc.2024.1900","url":null,"abstract":"<p><p>Emicizumab is a bispecific antibody that mimics the function of factor VIII (FVIII) and is indicated for prophylactic use in patients with congenital hemophilia A with or without inhibitors. Acquired hemophilia A (AHA) is a rare and severe disorder causes by autoantibodies that inhibit FVIII. In AHA, acute bleeding are managed with bypassing agents but several reports described the off-label use of emicizumab. The aim of this article is to describe two cases of AHA treated with emicizumab and a review of the scientific littérature. Reports indicate that the use of emicizumab is efficacious to treat acute bleeding with less thrombotic events thant with bypassing agents and with a reduced hospitalisation duration. Nevertheless biological monitoring is more complicated with assay interferences and a persistent circulation more than 6 months after the last injection was observed for our two patients.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 3","pages":"294-307"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141989719","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
[Feedback on the detection of SARS-CoV-2 by the point-of-care testing]. [关于使用护理点检测法检测 SARS-CoV-2 的反馈意见]。
Annales de biologie clinique Pub Date : 2024-08-30 DOI: 10.1684/abc.2024.1891
Jean-Claude Nguyen Van, Amir Khaterchi
{"title":"[Feedback on the detection of SARS-CoV-2 by the point-of-care testing].","authors":"Jean-Claude Nguyen Van, Amir Khaterchi","doi":"10.1684/abc.2024.1891","DOIUrl":"10.1684/abc.2024.1891","url":null,"abstract":"<p><p>In order to improve the detection and rapid diagnosis of the SARS-CoV-2 coronavirus, we evaluated the ID NOW™ COVID-19 isothermal gene amplification technique in parallel with the real-time PCR technique (Diasorin) routinely used in the laboratory during a prospective study in the 2020 season. As this technique showed satisfactory sensitivity and specificity of 98% and 97.5% respectively, we then proposed to implement the detection of SARS-CoV-2 coronavirus in the emergency department and maternity as a point-of-care test (POCT) for the 2020-2021 season and to evaluate its clinical and organizational impact. This article summarizes the results obtained and highlights the advantages and limitations of this strategy implemented in the emergency department, particularly in terms of time spent in the department, hospitalization rates, anticoagulant treatment and early isolation of patients, as well as the organizational impact on the maternity unit. Based on this experience, we report on the regulatory constraints that apply when setting up a POCT and the steps required to validate the accreditation in accordance with standard NF EN ISO 22870.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 3","pages":"281-293"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141319204","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
[Acute myeloid leukemia with mutated RUNX1 at the university hospitals of Strasbourg]. [斯特拉斯堡大学医院发生 RUNX1 基因突变的急性髓性白血病]。
Annales de biologie clinique Pub Date : 2024-08-30 DOI: 10.1684/abc.2024.1899
Baptiste Panaget, Laurent Mauvieux, Laurent Miguet, Luc-Mathieu Fornecker, Bruno Lioure, Marie-Pierre Ledoux, Delphine Rolland, Caroline Mayeur-Rousse
{"title":"[Acute myeloid leukemia with mutated RUNX1 at the university hospitals of Strasbourg].","authors":"Baptiste Panaget, Laurent Mauvieux, Laurent Miguet, Luc-Mathieu Fornecker, Bruno Lioure, Marie-Pierre Ledoux, Delphine Rolland, Caroline Mayeur-Rousse","doi":"10.1684/abc.2024.1899","DOIUrl":"10.1684/abc.2024.1899","url":null,"abstract":"<p><p>RUNX1 is essential during human hematopoiesis. Numerous RUNX1 deregulations have been described, including translocations and germline or somatic mutations. Recurrent de novo RUNX1 mutations in acute myeloid leukemias (AML) prompted the creation of a provisional entity of AML with mutated RUNX1 in the 2016 WHO. In addition, recent genomic studies underlined rare AML patients with plasmacytoid dendritic cell (pDC) expansion and high RUNX1 mutations frequency. To better characterized AML with RUNX1 mutations, we retrospectively investigated a cohort of 32 patients diagnosed at Strasbourg University Hospital. Detailed clinical and biological features were aggregated. The presence of a pDC contingent was assessed by cytology and flow cytometry. In our cohort, no common features were identified either in term of cytology, stage of leukemia arrest or mutational features. Based on our observations, mutated RUNX1 AMLs do not appear to be a distinct AML entity. The new 2022 WHO classification includes AML with mutated RUNX1 within AML myelodysplasia-related category. We also identified within our cohort a patient whose AML fulfilled AML-pDC criteria, a rare and newly included entity in the last WHO classification.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 3","pages":"266-280"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142115838","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
A case of t-cell lymphoblastic lymphoma characterized by pleural effusion combined with pericardial effusion. 一例以胸腔积液合并心包积液为特征的 t 细胞淋巴细胞淋巴瘤。
Annales de biologie clinique Pub Date : 2024-08-30 DOI: 10.1684/abc.2024.1897
Jiaqing Hu Mengmeng Wang, Jinlong Song
{"title":"A case of t-cell lymphoblastic lymphoma characterized by pleural effusion combined with pericardial effusion.","authors":"Jiaqing Hu Mengmeng Wang, Jinlong Song","doi":"10.1684/abc.2024.1897","DOIUrl":"10.1684/abc.2024.1897","url":null,"abstract":"<p><p>This case underscores the pivotal role of early cytological examination of bodily fluids in the preliminary detection of lymphoma, a conclusion reinforced by subsequent pathological findings and refined through immunohistochemical characterization. A morphological analysis of pleural effusion cells was conducted in a 25-year-old male presenting initially with concurrent pleural and pericardial effusions. Initial morphological assessment of effusion specimens indicated the likelihood of a lymphoproliferative disorder. Subsequent detailed pathological and immunohistochemical investigations confirmed this suspicion, culminating in a definitive diagnosis of T-cell lymphoblastic lymphoma (T-LBL). The case emphasizes the necessity of employing a comprehensive and synergistic diagnostic approach, facilitating prompt and accurate diagnosis and subtyping of lymphoma.</p>","PeriodicalId":93870,"journal":{"name":"Annales de biologie clinique","volume":"82 3","pages":"351-355"},"PeriodicalIF":0.0,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141989723","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
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