The course and outcome of pregnancy in patient with concomitant Gilbert syndrome and hereditary spherocytosis: a unique case report

被引:1
作者
Bapaveva, C. [1 ]
Terzic, M. [1 ,2 ,3 ]
Togyzbayeva, K. [1 ]
Bekenova, A. [2 ]
Terzic, S. [2 ]
机构
[1] Univ Med Ctr, Natl Res Ctr Mother & Child Hlth, Astana, Kazakhstan
[2] Nazarbayev Univ, Sch Med, Dept Med, Astana, Kazakhstan
[3] Univ Pittsburg, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA
关键词
Gilbert syndrome; Hereditary spherocytosis; Pregnancy outcome; High-risk pregnancy; INHERITED DISORDERS; SPLENECTOMY; DIAGNOSIS;
D O I
10.12891/ceog4599.2019
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Gilbert syndrome (GS) is an autosomal dominant mild unconjugated hyperbilirubinemia. Hereditary spherocytosis (HS) is an inherited condition of non-immune heterogeneous hemolytic anemia. These two diseases can be very rarely diagnosed in one patient, but there is not one case reported in pregnant patient. The authors present a unique case of concomitant both diseases in pregnancy. The patient was 25- years-old, conceived spontaneously, and carefully observed throughout the pregnancy. Considering that both diseases might have a detrimental influence on pregnancy course and outcome, especially in this case with severe form of HS, the woman was hospitalized and carefully observed until the end of pregnancy. She delivered vaginally without any feto-matemal complications. In conclusion, coexisting GS and HS during pregnancy deserve careful monitoring and up-to-date treatment. This case report shows that a contemporary approach to the pregnant patient with GS and HS can result in the delivery of a healthy baby without any complications.
引用
收藏
页码:320 / 322
页数:3
相关论文
共 50 条
  • [41] MASSIVE MEDIASTINAL EXTRAMEDULLARY HEMATOPOIESIS IN HEREDITARY SPHEROCYTOSIS - A CASE-REPORT
    BASTION, Y
    COIFFIER, B
    FELMAN, P
    ASSOULINE, D
    TIGAUD, JD
    ESPINOUSE, D
    BRYON, PA
    AMERICAN JOURNAL OF HEMATOLOGY, 1990, 35 (04) : 263 - 265
  • [42] A Unique Patient Presenting With Concomitant Klinefelter Syndrome, Alport Syndrome, and Craniopharyngioma
    Rotondi, Mario
    Fallerini, Chiara
    Pirali, Barbara
    Longo, Ilaria
    Pasquali, Daniela
    Rampino, Teresa
    Chiovato, Luca
    Mari, Francesca
    Renieri, Alessandra
    JOURNAL OF ANDROLOGY, 2012, 33 (06): : 1155 - 1159
  • [43] Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report
    Du, Zhanhui
    Luo, Gang
    Wang, Kuiliang
    Bing, Zhen
    Pan, Silin
    BMC PEDIATRICS, 2021, 21 (01)
  • [44] Pyoderma Gangrenosum in a Splenectomy Incision in a Patient with Haemolytic Anaemia due to Hereditary Spherocytosis: a Case Report and Literature Review
    Krajewski, Piotr K.
    Chlebicka, Iwona
    Szepietowski, Jacek C.
    Maj, Joanna
    ACTA DERMATO-VENEREOLOGICA, 2021, 101
  • [45] Splenic infarction after Epstein–Barr virus infection in a patient with hereditary spherocytosis: a case report and literature review
    Zhongwu Ma
    Zhejin Wang
    Xiaodan Zhang
    Haibo Yu
    BMC Surgery, 22
  • [46] Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case report
    Jiang, Ni
    Mao, Wu-Yong
    Peng, Bing-Xue
    Yang, Ting-Ya
    Mao, Xiao-Rong
    WORLD JOURNAL OF CLINICAL CASES, 2023, 11 (06) : 1349 - 1355
  • [47] Concomitant ulcerative colitis and Usher syndrome in a Pakistani patient: A novel case report
    Siddiqui, Fatima Zulfiqar
    Ashkar, Anusha
    Aamir, Saira Maryam
    SAGE OPEN MEDICAL CASE REPORTS, 2024, 12
  • [48] Giant right ventricular outflow tract thrombus in hereditary spherocytosis: A case report
    Davidsen C.
    Larsen T.H.
    Gerdts E.
    Lønnebakken M.T.
    Thrombosis Journal, 14 (1)
  • [49] Acenocoumarol and Pregnancy Outcome in a Patient with Mitral Valve Prosthesis: A Case Report
    Stefanidis, Konstantinos
    Papoutsis, Dimitris
    Daskalakis, George
    Loutradis, Dimitris
    Antsaklis, Aris
    FETAL DIAGNOSIS AND THERAPY, 2009, 25 (01) : 115 - 118
  • [50] The coincidence of beta-thalassemia and hereditary spherocytosis: A case report and literature review
    Habibzadeh, Sana
    Einakchi, Majid
    Kalantari, Mohammad Ebrahim
    Forouhar, Farnood
    Masouminejad, Arefeh
    CLINICAL CASE REPORTS, 2024, 12 (06):