Evidence map›Paper›PMID 41169931›Full record

ArticleInternational journal of women's health2025

Pregnancy-Triggered Hereditary Thrombotic Thrombocytopenic Purpura: A Case Report.

Xin Xing, Na Yu, Zhiwei Zhang

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Article in International journal of women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Xin XingDepartment of Obstetrics and Gynecology, the First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong Province, 250014, People's Republic of China.
Na YuReproductive Medicine Center, Key Laboratory of Maternal & Fetal Medicine of National Health Commission of China, Shandong Provincial Maternal and Child Health Care Hospital Affiliated to Qingdao University, Jinan, Shandong Province, 250014, People's Republic of China.
Zhiwei ZhangDepartment of Obstetrics and Gynecology, the First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong Province, 250014, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hereditary thrombotic thrombocytopenic purpura (hTTP), as an autosomal recessive hereditary disease, pregnancy is one of its recognized trigger factors. The lag in the diagnosis and treatment of this disease can lead to serious adverse pregnancy outcomes. In clinical practice, a high degree of vigilance should be maintained and timely treatment should be given to strive for better pregnancy outcomes. Case Presentation: A 36-year-old woman has undergone 4 pregnancies over a period of 25 years. Due to the insufficient diagnosis capabilities at that time, it was not until the 3rd pregnancy when the patient again presented with severe thrombocytopenia in the second trimester that she was diagnosed with hTTP in our hospital. However, since the optimal treatment opportunity was missed, even though active plasma infusion was carried out, fetal death still occurred. In 2024, the patient got pregnant again, and this was her 4th pregnancy. During this pregnancy, the patient underwent preventive plasma infusion therapy throughout and no serious complications emerged. Ultimately, she gave birth to a full-term baby in February 2025. Conclusion: We report a case of hTTP caused by complex compound heterozygous gene mutations. Currently, pregnancy is the only trigger for the patient's illness. Timely identification, early differential diagnosis from obstetric complications, and active management are crucial for improving the pregnancy outcome of hTTP patients. We adopted a more conservative strategy of prophylactic plasma infusion during pregnancy and also achieved good maternal and fetal outcomes.

Indexed as

ADAMTS13case reporthereditary thrombotic thrombocytopenic purpurapregnancythrombotic microangiopathy

Identifiers

PMID41169931
PMCPMC12570972

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