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      The case of undiagnosed immunodeficiency in child from mother with leukemia anamnesis

      case-report

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          Abstract

          Acute lymphoblastic leukemia (ALL) in pregnant women is rare experience, but it can complicate the gestation by increasing the risk of miscarriage and premature birth. However, the adequate carrying of the pregnancy is possible for women who suffered from leukemia in childhood and achieved the remission during the treatment. Furthermore, there are some facts about the possibility of immunosuppression in children whose parents suffer from various immunodeficiency disorders, including ALL. This clinical case demonstrates the importance of correct diagnostics in order to reveal the congenital pathologies of the immune system in children, whose parents suffered from lymphocytic leukemia, even in case of full clinical and laboratory remission for a significant period of time. In the hospital, the thread metric approach was used for sepsis diagnostics. Conducted treatment was ineffective due to the inadequate immune response in the child and lack of the targeted adjusted measures to immunodeficiency disorder. The present case demonstrates the congenital T-cells immunodeficiency in a child who was complicated by the development of acute ulceronecrotic enterocolitis after vaccination. The treatment that was targeted mainly at the agent eradication did not give the desired results due to non-responsiveness of the immune system of the child.

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          Biology, risk stratification, and therapy of pediatric acute leukemias: an update.

          We review recent advances in the biologic understanding and treatment of childhood acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML), identify therapeutically challenging subgroups, and suggest future directions of research. A review of English literature on childhood acute leukemias from the past 5 years was performed. Contemporary treatments have resulted in 5-year event-free survival rates of approximately 80% for childhood ALL and almost 60% for pediatric AML. The advent of high-resolution genome-wide analyses has provided new insights into leukemogenesis and identified many novel subtypes of leukemia. Virtually all ALL and the vast majority of AML cases can be classified according to specific genetic abnormalities. Cooperative mutations involved in cell differentiation, cell cycle regulation, tumor suppression, drug responsiveness, and apoptosis have also been identified in many cases. The development of new formulations of existing drugs, molecularly targeted therapy, and immunotherapies promises to further advance the cure rates and improve quality of life of patients. The application of new high-throughput sequencing techniques to define the complete DNA sequence of leukemia and host normal cells and the development of new agents targeted to leukemogenic pathways promise to further improve outcome in the coming decade.
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            Cancer, pregnancy and fertility: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.

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              Acute lymphoblastic leukaemia in adult patients: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

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                Author and article information

                Journal
                imas
                IMAS
                Interventional Medicine and Applied Science
                IMAS
                Akadémiai Kiadó (Budapest )
                2061-1617
                2061-5094
                26 October 2018
                December 2018
                : 10
                : 4
                : 216-221
                Affiliations
                [ 1 ]Department of Pediatrics, Sumy State University , Sumy, Ukraine
                [ 2 ]Department of Pathology, Sumy State University , Sumy, Ukraine
                [ 3 ]Department of Neurosurgery and Neurology, Sumy State University , Sumy, Ukraine
                [ 4 ]Department of Normal Anatomy, Kharkiv National Medical University , Kharkiv, Ukraine
                [ 5 ] Sumy Regional Clinical Perinatal Center , Sumy, Ukraine
                Author notes
                [* ]Corresponding author: Vladyslav Sikora, MD, PhD; Department of Pathology, Sumy State University, st. Privokzalnaya 31, m. Sumy 40022, Ukraine; Phone: +380 507 276 193; Fax: +380 0542 33 40 58; E-mail: v.sikora@ 123456med.sumdu.edu.ua
                Article
                10.1556/1646.10.2018.46
                6376359
                bdb9183e-5bed-4929-be19-4b6f6d2cb5c5
                © 2018 The Author(s)

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium for non-commercial purposes, provided the original author and source are credited, a link to the CC License is provided, and changes – if any – are indicated.

                History
                : 25 May 2018
                : 17 August 2018
                : 04 September 2018
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 22, Pages: 6
                Funding
                Funding sources: No financial support was received for this study.
                Categories
                CASE REPORT

                Medicine,Immunology,Health & Social care,Microbiology & Virology,Infectious disease & Microbiology
                thymus,spleen,immunodeficiency,acute lymphoblastic leukemia,vaccination,immune system

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