电邮这篇文章 Iatrogenic chimerism in a patient with Fanconi anemia and delayed puberty
- 作者: Kumykova Z.K.1, Kiseleva I.A.1, Batyrova Z.K.1, Buyanovskaya O.A.1
-
隶属关系:
- Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
- 期: 卷 22, 编号 2 (2020)
- 页面: 35-37
- 栏目: CLINICAL CASE
- URL: https://bakhtiniada.ru/2079-5831/article/view/34048
- DOI: https://doi.org/10.26442/20795696.2020.2.200108
- ID: 34048
如何引用文章
全文:
详细
The article presents a clinical case of delayed puberty in a 13-year-old girl with Fanconi anemia who was sent to the Department of gynecology of children and adolescents for removal of the sexual glands due to the detection of a Y-chromosome in the karyotype at the place of residence. A personalized multidisciplinary approach to the management of a patient with Fanconi anemia with the presence of the Y-chromosome in the karyotype against the background of delayed puberty allowed to identify iatrogenic chimerism and avoid unjustified castration.
作者简介
Zaira Kumykova
Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
编辑信件的主要联系方式.
Email: zai-kumykova@yandex.ru
Cand. Sci. (Med.)
俄罗斯联邦, MoscowIrina Kiseleva
Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: iakiseleva@mail.ru
ORCID iD: 0000-0003-2493-090X
Cand. Sci. (Med.)
俄罗斯联邦, MoscowZalina Batyrova
Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: iakiseleva@mail.ru
ORCID iD: 0000-0003-4997-6090
Cand. Sci. (Med.)
俄罗斯联邦, MoscowOlga Buyanovskaya
Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: o_buyanovskaya@oparina4.ru
Cand. Sci. (Med.)
俄罗斯联邦, Moscow参考
- Fiesco-Roa MO, Giri N, McReynolds LJ et al. Genotypephenotype associations in Fanconi anemia: A literature review. Blood Rev 2019; 37. https://doi.org/10.1016/j.blre.2019.100589
- Shimamura A, Alter BP. Pathophysiology and management of inherited bone marrow failure syndromes. Blood Rev 2010; 24 (3): 101–22.
- Alter BP, Giri N, Savage SA, Rosenberg PS. Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up. Haematologica 2018; 103 (1): 30–9.
- Rodriguez A, D’Andrea A. Fanconi anemia pathway. Curr Biol 2017; 27 (18): R986-r8.
- McCann S, Lawler M. Mixed chimerism; detection and significance following BMT. Bone Marrow Translant 1993; 11: 91–4.
- Tippet P. Blood group chimeras: A review. Vox Sang 1983; 44: 333–59.
- Bader P, Niethammer D, Willasch A et al. How and when should we monitor chimerism after allogeneic stem cell transplantation? Bone Marrow Transplant 2005; 35 (2): 107–19.
补充文件
