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Pediatria Polska最新文献

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Fatal Waterhouse-Friderichsen syndrome due to Neisseriameningitidis group B in a paediatric patient duringthe phone consultation era 在电话咨询时代，一名儿科患者因B组奈瑟菌性脑膜炎引起的致死性沃特豪斯-弗里德里克森综合征
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.125063
Marta Serafin, E. Czerwińska, Marian Koźbiał, M. Leszczyński, L. Szenborn
{"title":"Fatal Waterhouse-Friderichsen syndrome due to Neisseria\u0000meningitidis group B in a paediatric patient during\u0000the phone consultation era","authors":"Marta Serafin, E. Czerwińska, Marian Koźbiał, M. Leszczyński, L. Szenborn","doi":"10.5114/polp.2023.125063","DOIUrl":"https://doi.org/10.5114/polp.2023.125063","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70500587","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
Personalized multi-marker panel in the risk assessment of atopic dermatitis phenotypes in children 儿童特应性皮炎表型风险评估的个性化多标记面板
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.128063
V. Dytiatkovskyi, O. Abaturov, V. Dosenko, T. Drevytska, T. Lapikova-Bryhinska, Nataliya Naumenko, O. Alifirenko
{"title":"Personalized multi-marker panel in the risk assessment of atopic dermatitis phenotypes in children","authors":"V. Dytiatkovskyi, O. Abaturov, V. Dosenko, T. Drevytska, T. Lapikova-Bryhinska, Nataliya Naumenko, O. Alifirenko","doi":"10.5114/polp.2023.128063","DOIUrl":"https://doi.org/10.5114/polp.2023.128063","url":null,"abstract":"Introduction: This paper reports the study of a combined genetic and biomarker panel for assessing the risk of development of different phenotypes of atopic dermatitis (AD) in children: alone and combined with other atopic disorders (AtD) – allergic rhinitis/rhino-conjunctivitis (AR/ARC) and bronchial asthma (BA). The aim was to establish a personalized diagnostic multi-marker panel for assessing the developmental risk of different AD phenotypes in children combining single nucleotide polymorphism (SNP) rs_7927894 filaggrin (FLG) genotype variants, serum levels of total immune globulin E (IgE), cutaneous T-cell attracting chemokine (CTACK/CCL27) and thymus and activation regulated chemokine (TARC/CCL17). Material and methods: The study recruited patients aged 3–18 years old: 39 atopic patients to the main group and 47 non-atopic patients to the control group. All the patients were tested for SNP variants of rs_7927894 FLG and serum concentrations of total IgE, CTACK/CCL27 and TARC/CCL17. Results: Within AD alone phenotype patients we detected the following significant risk ratios: cytosinethymine (C/T) rs_7927894 FLG [odds ratio (OR) = 4.14, p < 0.05], total IgE > 173 IU/ml (OR = 8.98, p < 0.001), CTACK/ CCL27 > 3658.5 pg/ml (OR = 5.64, p < 0.01). Atopic disorders combined with other AtD phenotype: C/T rs_7927894 FLG (OR = 2.88, p < 0.05), total IgE > 213 IU/ml (OR = 136.7, p < 0.001), CTACK/CCL27 > 4308.8 pg/ml (OR = 7.40, p < 0.001). With AD combined with other AtD collated to AD alone – total IgE > 1001 IU/ml (OR = 16.0, p < 0.001). TARC/CCL17 had no significant differences among main and control groups. Conclusions: Cytosinethymine rs_7927894 FLG variant combined with cut-off serum IgE and CTACK/ CCL27 levels is a novel significant personalized multi-marker panel for assessing the risk of development of the different AD phenotypes in children.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70501255","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
Cough as a symptom of respiratory infection or a rare cardiological pathology in an infant 咳嗽作为呼吸道感染的症状或婴儿罕见的心脏病病理
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.130846
Anna Chanas, Klaudia Obsznajczyk, B. Kucińska, Bożena Werner
{"title":"Cough as a symptom of respiratory infection or a rare cardiological pathology in an infant","authors":"Anna Chanas, Klaudia Obsznajczyk, B. Kucińska, Bożena Werner","doi":"10.5114/polp.2023.130846","DOIUrl":"https://doi.org/10.5114/polp.2023.130846","url":null,"abstract":"Congenital coronary artery anomalies are rare and represent 0.24–0.46% of all congenital heart defects. The most common is an anomaly in which the left coronary artery arises from the pulmonary artery (ALCAPA), also known as a Bland-White-Garland syndrome. Nonspecific symptoms typically appear at 2–3 months of age. We present the case of a 10-week-old boy admitted to the hospital due to cough and dyspnea, with suspicion of a respiratory tract infection with no clinical improvement after standard therapy. The chest X-ray revealed cardiomegaly. The electrocardiogram showed signs of anterolateral infarction. Echocardiography revealed signs of dilatated cardiomyopathy and color Doppler was of great value in establishing a final diagnosis. After confirming the diagnosis of ALCAPA in computed tomography angiography, the patient was operated on, with a good outcome.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70502388","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
Blood group relevance for the newborn – the ABO system and neonatal diseases 血型相关性的新生儿- ABO系统和新生儿疾病
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.125423
Izabela M Cendal, B. Królak-Olejnik
{"title":"Blood group relevance for the newborn – the ABO system and neonatal diseases","authors":"Izabela M Cendal, B. Królak-Olejnik","doi":"10.5114/polp.2023.125423","DOIUrl":"https://doi.org/10.5114/polp.2023.125423","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70501028","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
Psychological and functional problems of children and adolescents with cerebral palsy from the neurodevelopmental perspective 从神经发育角度看儿童和青少年脑瘫的心理和功能问题
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.128854
P. Rok-Bujko, Joanna Kawecka
{"title":"Psychological and functional problems of children and adolescents with cerebral palsy from the neurodevelopmental perspective","authors":"P. Rok-Bujko, Joanna Kawecka","doi":"10.5114/polp.2023.128854","DOIUrl":"https://doi.org/10.5114/polp.2023.128854","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"51 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70502177","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
Anti-SARS-CoV-2 antibodies important in diagnostics of acute hepatitis in children 抗sars - cov -2抗体在儿童急性肝炎诊断中的重要意义
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.125696
M. Pawłowska, J. Moppert, Małgorzata Sobolewska-Pilarczyk
{"title":"Anti-SARS-CoV-2 antibodies important in diagnostics of acute hepatitis in children","authors":"M. Pawłowska, J. Moppert, Małgorzata Sobolewska-Pilarczyk","doi":"10.5114/polp.2023.125696","DOIUrl":"https://doi.org/10.5114/polp.2023.125696","url":null,"abstract":"The most common causes of acute hepatitis in children are hepatitis A and autoimmune hepatitis. Hepatitis in the course of Wilson's disease is sporadically registered in adolescents. An increase of activity of aminotransferases both in the course of multisystem inflammatory syndrome in children (MIS-C) and in the course of COVID-19 has been observed. Hepatitis is common in children with MIS-C and is associated with a more severe presentation and persistent elevation of liver function tests. To date, no cases of acute hepatitis in children due to COVID-19 have been reported. We present 2 cases of acute hepatitis in children where the only cause seems to be a previous asymptomatic SARS-CoV-2 infection.Copyright © 2023 Termedia Publishing House Ltd.. All rights reserved.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70500825","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
Significance of anti-endothelial cell antibodies in paediatrickidney transplant recipients 抗内皮细胞抗体在儿童肾移植受者中的意义
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.125388
Mervat Ismail, F. Fadel, A. Rashad, Doaa M. Salah, M. Rasheed, N. Kantoush, Mona H. Ibrahim, M. Kafoury, Manal F Elshamaa
{"title":"Significance of anti-endothelial cell antibodies in paediatric\u0000kidney transplant recipients","authors":"Mervat Ismail, F. Fadel, A. Rashad, Doaa M. Salah, M. Rasheed, N. Kantoush, Mona H. Ibrahim, M. Kafoury, Manal F Elshamaa","doi":"10.5114/polp.2023.125388","DOIUrl":"https://doi.org/10.5114/polp.2023.125388","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70500972","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
Functional annotation of lactase gene and its distal enhancer MCM6 for prediction of metabolically unhealthy obesity 乳糖酶基因及其远端增强子MCM6预测代谢不健康肥胖的功能注释
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.126132
A. Abaturov, A. Nikulina
{"title":"Functional annotation of lactase gene and its distal enhancer MCM6 for prediction of metabolically unhealthy obesity","authors":"A. Abaturov, A. Nikulina","doi":"10.5114/polp.2023.126132","DOIUrl":"https://doi.org/10.5114/polp.2023.126132","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"11 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70501279","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 thrombotic thrombocytopaenic purpura of an atypical, oligosymptomatic course in an adolescent girl – case report 获得性血栓性血小板减少性紫癜的一个不典型，少症状的过程中，在青春期的女孩-个案报告
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.127966
Grażyna Waśka, Weronika Fijałkowska, Marta Badeńska, Andrzej Badeński, Agnieszka A. Książek, R. Tomaszewska, E. Trembecka-Dubel, M. Szczepańska
{"title":"Acquired thrombotic thrombocytopaenic purpura of an atypical, oligosymptomatic course in an adolescent girl – case report","authors":"Grażyna Waśka, Weronika Fijałkowska, Marta Badeńska, Andrzej Badeński, Agnieszka A. Książek, R. Tomaszewska, E. Trembecka-Dubel, M. Szczepańska","doi":"10.5114/polp.2023.127966","DOIUrl":"https://doi.org/10.5114/polp.2023.127966","url":null,"abstract":"","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70501464","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
Atypical mycobacterial cervical lymphadenopathy in a 2-year-old girl 2岁女童非典型分枝杆菌性宫颈淋巴结病
Pediatria Polska Pub Date : 2023-01-01 DOI: 10.5114/polp.2023.128800
Anna Fedorowicz, M. Pasierbek, W. Korlacki
{"title":"Atypical mycobacterial cervical lymphadenopathy in a 2-year-old girl","authors":"Anna Fedorowicz, M. Pasierbek, W. Korlacki","doi":"10.5114/polp.2023.128800","DOIUrl":"https://doi.org/10.5114/polp.2023.128800","url":null,"abstract":"Lymphadenopathy is a common clinical condition in the paediatric population. In 50% of cases it occurs in otherwise healthy children, and in 75% it presents as a localized form. Lymphadenopathy lasting more than 3 months is defined as chronic. Common conditions causing lymph node enlargement include infections, malignancies, and autoimmune disorders. Mycobacteria causing infectious lymphadenopathy are divided into tuberculous and non-tuberculous mycobacteria (NTM). Diagnosing mycobacterial disease is complicated, and definitive surgery is the best treatment option for NTM cervicofacial lymphadenitis. We present a case of a 2-year-old girl with chronic cervical lymphadenopathy, eventually diagnosed as NTM infection. The diagnostic and therapeutic process was complicated, demanding an interdisciplinary approach and several surgical procedures. The treatment was supported by negative pressure therapy.","PeriodicalId":39653,"journal":{"name":"Pediatria Polska","volume":"29 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70501814","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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