Klaudia Korecka

Medical University of Silesia

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Tomasz Koszutski

Medical University of Silesia

Grzegorz Kudela

Medical University of Silesia

Lidia Hyla‐Klekot

Medical University of Silesia

Wojciech Korlacki

Medical University of Silesia

Agnieszka Pastuszka

Medical University of Silesia

Franciszek Halkiewicz

Górnośląskie Centrum Medyczne

Jakub Behrendt

Medical University of Silesia

Sabina Więcek

Medical University of Silesia

Maria Sąsiadek

Wroclaw Medical University

Monika Pietrowska

The Maria Sklodowska-Curie National Research Institute of Oncology

Cooperative Institutions

Medical University of Silesia

Górnośląskie Centrum Medyczne

University of Silesia in Katowice

Górnośląskie Centrum Zdrowia Dziecka w Katowicach

Wroclaw Medical University

Silesian Center for Heart Disease

University of Wrocław

John Paul II Hospital

The Maria Sklodowska-Curie National Research Institute of Oncology

University of Economics in Katowice

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Congenital Sternal Cleft—A Case Report

Advances in respiratory medicine (2011)

Franciszek Halkiewicz Klaudia Korecka Wojciech Korlacki Jakub Behrendt

Sternal cleft is a very rare congenital defect of the sternum, reported only in a limited number of publications. Surgical treatment in the neonatal period is preferred. A case of a child with congenital sternal cleft operated on at 17 months of age with a successful outcome of repair was reported.

Sternum

Congenital malformations

10.5603/arm.27627

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Citations (2)

Foreign body aspiration in children: diagnostic and therapeutic role of bronchoscopy

Pediatric Surgery International (2011)

Wojciech Korlacki Klaudia Korecka Józef Dzielicki

Assessment of bronchoscopy usefulness for diagnosis and treatment in children suspected of foreign body aspiration.There were 27 boys and 18 girls in the age from 15 month to 14 years (average 5.5 years). Rigid bronchoscopy was performed under general anaesthesia. Assessment of the respiratory tract was done and in cases with foreign body bronchoscopic evacuation was executed. Medical records and video recordings of bronchoscopy procedures were subjected to retrospective analysis.In 28 children (62.2%) during bronchoscopy, foreign body aspiration recognized in 17 (37.8%) bronchoscopy cases was negative. In 27 patients, foreign bodies were removed. In one child, foreign body was evacuated during second bronchoscopy after preparing proper instrumentation. There were no complications in post-bronchoscopic period. Operating time was from 5 to 90 min, average time was noted to be 24 min. Average time of hospital stay was 2-3 days.Aspiration of foreign body should be suspected in all cases of bronchopulmonary infection with atypical course. Bronchoscopy is the best diagnostic and therapeutic method in all suspicions of foreign body. In children rigid bronchoscopy is still the method of choice.

Foreign body aspiration

Foreign Body Removal

Flexible bronchoscopy

Rigid bronchoscopy

10.1007/s00383-011-2874-8

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Citations (84)

Proteomics of urinary small extracellular vesicles in early diagnosis of kidney diseases in children‐expectations and limitations

PROTEOMICS (2024)

Klaudia Korecka Marta Gawin Agnieszka Pastuszka Mirosław Partyka Tomasz Koszutski

Abstract The primary function of the kidneys is to maintain systemic homeostasis (disruption of renal structure and function results in multilevel impairment of body function). Kidney diseases are characterized by a chronic, progressive course and may result in the development of chronic kidney disease (CKD). Evaluation of the composition of the proteome of urinary small extracellular vesicles (sEVs) as a so‐called liquid biopsy is a promising new research direction. Knowing the composition of sEV could allow localization of cellular changes in specific sections of the nephron or the interstitial tissue before fixed changes, detectable only at an advanced stage of the disease, occur. Research is currently underway on the role of sEVs in the diagnosis and monitoring of many disease entities. Reports in the literature on the subject include: diabetic nephropathy, focal glomerulosclerosis in the course of glomerulopathies, renal fibrosis of various etiologies. Studies on pediatric patients are still few, involving piloting if small groups of patients without validation studies. Here, we review the literature addressing the use of sEV for diagnosis of the most common urinary disorders in children. We evaluate the clinical utility and define limitations of markers present in sEV as potential liquid biopsy.

Extracellular Vesicles

10.1002/pmic.202300168

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Citations (2)

Alternations in genes expression of pathway signaling in esophageal tissue with atresia: results of expression microarray profiling

Diseases of the Esophagus (2014)

Robert Śmigiel Arleta Lebioda Michał Błaszczyński Klaudia Korecka Piotr Czauderna

Esophageal atresia (EA) is a congenital defect of the esophagus involving the interruption of the esophagus with or without connection to the trachea (tracheoesophageal fistula [TEF]). EA/TEF may occur as an isolated anomaly, may be part of a complex of congenital defects (syndromic), or may develop within the context of a known syndrome or association. The molecular mechanisms underlying the development of EA are poorly understood. It is supposed that a combination of multigenic factors and epigenetic modification of genes play a role in its etiology. The aim of our work was to assess the human gene expression microarray study in esophageal tissue samples. Total RNA was extracted from 26 lower pouches of esophageal tissue collected during thoracoscopic EA repair in neonates with the isolated (IEA) and the syndromic form (SEA). We identified 787 downregulated and 841 upregulated transcripts between SEA and controls, and about 817 downregulated and 765 upregulated probes between IEA and controls. Fifty percent of these genes showed differential expression specific for either IEA or SEA. Functional pathway analysis revealed substantial enrichment for Wnt and Sonic hedgehog, as well as cytokine and chemokine signaling pathways. Moreover, we performed reverse transcription polymerase chain reaction study in a group of SHH and Wnt pathways genes with differential expression in microarray profiling to confirm the microarray expression results. We verified the altered expression in SFRP2 gene from the Wnt pathway as well as SHH, GLI1, GLI2, and GLI3 from the Sonic hedgehog pathway. The results suggest an important role of these pathways and genes for EA/TEF etiology.

GLI1

GLI2

Tracheoesophageal Fistula

10.1111/dote.12173

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Citations (8)

Spontaneous resolution of pneumomediastinum in children – clinical experience

Pediatria Polska (2019)

Klaudia Korecka Lidia Hyla‐Klekot Mateusz Kęsek Grzegorz Kudela Andrzej M. Bulandra

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Korecka K, Hyla-Klekot L, Kęsek M, Kudela G, Bulandra A, Koszutski T. Spontaneous resolution of pneumomediastinum in children – clinical experience. Pediatria Polska - Polish Journal of Paediatrics. 2019;94(2):105-110. doi:10.5114/polp.2019.85039. APA Korecka, K., Hyla-Klekot, L., Kęsek, M., Kudela, G., Bulandra, A., & Koszutski, T. (2019). Spontaneous resolution of pneumomediastinum in children – clinical experience. Pediatria Polska - Polish Journal of Paediatrics, 94(2), 105-110. https://doi.org/10.5114/polp.2019.85039 Chicago Korecka, Klaudia, Lidia Hyla-Klekot, Mateusz Kęsek, Grzegorz Kudela, Andrzej Michał Bulandra, and Tomasz Koszutski. 2019. "Spontaneous resolution of pneumomediastinum in children – clinical experience". Pediatria Polska - Polish Journal of Paediatrics 94 (2): 105-110. doi:10.5114/polp.2019.85039. Harvard Korecka, K., Hyla-Klekot, L., Kęsek, M., Kudela, G., Bulandra, A., and Koszutski, T. (2019). Spontaneous resolution of pneumomediastinum in children – clinical experience. Pediatria Polska - Polish Journal of Paediatrics, 94(2), pp.105-110. https://doi.org/10.5114/polp.2019.85039 MLA Korecka, Klaudia et al. "Spontaneous resolution of pneumomediastinum in children – clinical experience." Pediatria Polska - Polish Journal of Paediatrics, vol. 94, no. 2, 2019, pp. 105-110. doi:10.5114/polp.2019.85039. Vancouver Korecka K, Hyla-Klekot L, Kęsek M, Kudela G, Bulandra A, Koszutski T. Spontaneous resolution of pneumomediastinum in children – clinical experience. Pediatria Polska - Polish Journal of Paediatrics. 2019;94(2):105-110. doi:10.5114/polp.2019.85039.

Pneumomediastinum

Hyla

10.5114/polp.2019.85039

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Citations (1)

Duodenal obstruction in prenatal ultrasound examinations - duodenal atresia versus annular pancreas - reports on two cases and literature review

Prenatal Cardiology (2021)

Klaudia Korecka Maria Respondek‐Liberska

Duodenal Atresia

Annular pancreas

Prenatal ultrasound

Neonatology

10.12847/06145

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No Appendix is Too Short—Simultaneous Mitrofanoff Catheterizable Vesicostomy and Malone Antegrade Continence Enema (MACE) for Children with Spina Bifida

Urology (2018)

Grzegorz Kudela Dominika Smyczek Alexander Springer Klaudia Korecka Tomasz Koszutski

Mace

Enema

Stoma (medicine)

Bladder augmentation

10.1016/j.urology.2018.03.014

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Citations (11)

Pneumatosis intestinalis as a complication of acute diarrhoea in children

Pediatria Polska (2018)

Sabina Więcek Urszula Grzybowska-Chłebowczyk Zbigniew Olczak Katarzyna Gruszczyńska Klaudia Korecka

ENWEndNote BIBJabRef, Mendeley RISPapers, Reference Manager, RefWorks, Zotero AMA Więcek S, Grzybowska-Chlebowczyk U, Olczak Z, Gruszczyńska K, Korecka K, Koszutski T. Pneumatosis intestinalis as a complication of acute diarrhoea in children. Pediatria Polska - Polish Journal of Paediatrics. 2018;93(4):291-297. doi:10.5114/polp.2018.77993. APA Więcek, S., Grzybowska-Chlebowczyk, U., Olczak, Z., Gruszczyńska, K., Korecka, K., & Koszutski, T. (2018). Pneumatosis intestinalis as a complication of acute diarrhoea in children. Pediatria Polska - Polish Journal of Paediatrics, 93(4), 291-297. https://doi.org/10.5114/polp.2018.77993 Chicago Więcek, Sabina, Urszula Grzybowska-Chlebowczyk, Zbigniew Olczak, Katarzyna Gruszczyńska, Klaudia Korecka, and Tomasz Koszutski. 2018. "Pneumatosis intestinalis as a complication of acute diarrhoea in children". Pediatria Polska - Polish Journal of Paediatrics 93 (4): 291-297. doi:10.5114/polp.2018.77993. Harvard Więcek, S., Grzybowska-Chlebowczyk, U., Olczak, Z., Gruszczyńska, K., Korecka, K., and Koszutski, T. (2018). Pneumatosis intestinalis as a complication of acute diarrhoea in children. Pediatria Polska - Polish Journal of Paediatrics, 93(4), pp.291-297. https://doi.org/10.5114/polp.2018.77993 MLA Więcek, Sabina et al. "Pneumatosis intestinalis as a complication of acute diarrhoea in children." Pediatria Polska - Polish Journal of Paediatrics, vol. 93, no. 4, 2018, pp. 291-297. doi:10.5114/polp.2018.77993. Vancouver Więcek S, Grzybowska-Chlebowczyk U, Olczak Z, Gruszczyńska K, Korecka K, Koszutski T. Pneumatosis intestinalis as a complication of acute diarrhoea in children. Pediatria Polska - Polish Journal of Paediatrics. 2018;93(4):291-297. doi:10.5114/polp.2018.77993.

Pneumatosis Intestinalis

Acute diarrhea

10.5114/polp.2018.77993

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Zastosowanie terapii podciśnieniowej oraz hiperbarii w leczeniu rozległego urazu kończyny górnej na tle próby samobójczej – opis przypadku

Leczenie Ran (2016)

Agnieszka Pastuszka Katarzyna Byrka-Owczarek Klaudia Korecka Agnieszka Burkacka Tomasz Koszutski

10.15374/lr2016017

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Superior Mesenteric Artery Syndrome with: Gastric Emphysema, Gas in the Portal Vein and Pneumoperitoneum Due to Anorexia Nervosa

Journal of Food & Nutritional Disorders (2018)

Klaudia Korecka Grzegorz Kudela Magdalena Lucyga Małgorzata Janas–Kozik Ireneusz Jelonek

12- year- old patient suffering from anorexia nervosa feeding implementation after a period of prolonged fasting cause a refeeding syndrome, which manifests itself as acute electrolytes deficiency resulting in dysfunction of the entire organism, including bowel transit time disorders. Gastric antral electrical dysarhythmias which develop in this mechanism promote dilatation of the stomach. Concomitant compression and obstruction of the third portion of the duodenum due to superior mesenteric artery syndrome (Superior Mesenteric Artery syndrome) results in stomach dilatation, which can lead to gastric emphysema and pneumoperitoneum. The pathomechanisms described above create a vicious circle mechanism general symptom in the young patient.Gastric emphysema with gas in the portal vein and Superior mesenteric artery syndrome are potentially threatening complications of chronic malnutrition and anorexia. Intensive conservative treatment with a control CT scan after 24 to 48 hours may be useful when making the decision to withdraw from surgical procedure. Releasing the duodenum from the compression gives the opportunity to eliminate one element of the vicous circle mechanism as far as the treatment of eating disorders is concerned.

Anorexia nervosa

10.4172/2324-9323.1000240

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