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A severe case of pemphigoid gestationis persisting after labour - case report and review of the literature

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023698%3A_____%2F24%3AN0000008" target="_blank" >RIV/00023698:_____/24:N0000008 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11120/24:43925255 RIV/00064173:_____/24:43925255

  • Result on the web

    <a href="https://pubmed.ncbi.nlm.nih.gov/36919665/" target="_blank" >https://pubmed.ncbi.nlm.nih.gov/36919665/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5507/bp.2023.010" target="_blank" >10.5507/bp.2023.010</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A severe case of pemphigoid gestationis persisting after labour - case report and review of the literature

  • Original language description

    Background and Aim. Pemphigoid gestationis (PG) is a rare skin disease of pregnancy. Given its incidence in pregnant women, physicians and especially obstetricians may not encounter this diagnosis in their entire career. We find this to be a major problem and there is an obligation to report it in as much detail as possible along with recommended treatments with proven efficacy. Case report. We describe the case of a 27 year old patient who was referred to the dermatology department with severe dissemination of blisters in the 9th week of pregnancy. She was diagnosed with pemphigoid gestationis in her first pregnancy. High doses of corticosteroids were initiated but due to inadequate effect cyclosporine was added. The pregnancy was complicated with gestational diabetes. The patient gave birth in her 33rd week by caesarian section due to premature rupture of the membrane. Vesicles were seen on the newborn immediately after birth which diminished spontaneously over 2 weeks. Blisters were still seen on the patient 1 month after labor even with the combination of systemic corticosteroids with cyclosporine. Conclusion. PG is a rare dermatosis of pregnancy. The course of the disease can be severe, necessitating systemic therapy. As described in this patient, systemic corticosteroids may not be sufficient and adding another immunosuppressive treatment may be needed. If pemphigoid gestationis has occurred during a previous pregnancy it is advised to reconsider another pregnancy.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30214 - Obstetrics and gynaecology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    BIOMEDICAL PAPERS-OLOMOUC

  • ISSN

    1213-8118

  • e-ISSN

    1804-7521

  • Volume of the periodical

    168

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    5

  • Pages from-to

    271-275

  • UT code for WoS article

    000953967600001

  • EID of the result in the Scopus database

    2-s2.0-85204511442