Evidence map›Paper›PMID 42622037›Full record

ArticleCureus2026

A Case of Refractory Thrombocytopenia in Pregnancy.

David B Joseph, Andrea Bequest, Pinky Jha, Hetvi Patel

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In one paragraph

Article in Cureus, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

David B JosephDepartment of Family Medicine, Medical College of Wisconsin, Milwaukee, USA.
Andrea BequestDepartment of Internal Medicine, Medical College of Wisconsin, Milwaukee, USA.
Pinky JhaDepartment of Internal Medicine, Medical College of Wisconsin, Milwaukee, USA.
Hetvi PatelDepartment of Internal Medicine, Medical College of Wisconsin, Milwaukee, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune thrombocytopenia is an acquired autoimmune disorder characterized by isolated thrombocytopenia due to antibody-mediated platelet destruction and impaired platelet production. Thrombocytopenia in pregnancy is common, but severe thrombocytopenia requires prompt evaluation to distinguish benign gestational thrombocytopenia from immune thrombocytopenia, hypertensive disorders of pregnancy, hemolysis, elevated liver enzymes, low platelet count syndrome, and thrombotic microangiopathies. We present the case of a 19-year-old gravida 1 para 0 patient with sickle cell trait and iron deficiency anemia who was initially diagnosed with pregnancy-associated immune thrombocytopenia in the first trimester after presenting with severe thrombocytopenia, with a platelet count of 9 × 10³/µL. She initially responded to intravenous immunoglobulin and corticosteroids, with platelet recovery to 107 × 10³/µL during hospitalization and 264 × 10³/µL shortly after discharge. However, despite outpatient hematology follow-up and prednisone therapy, her platelet count progressively declined. She was readmitted at 22 weeks and 5 days of gestation after routine obstetric laboratory testing showed relapsing severe thrombocytopenia with platelets of 15 × 10³/µL. The patient was otherwise asymptomatic, aside from intermittent blood-tinged nasal discharge and mild vaginal spotting a few days before presentation that resolved spontaneously. She was normotensive and had no evidence of hemolysis, renal dysfunction, significant hepatic dysfunction, or coagulopathy. Hematology and maternal-fetal medicine were consulted, and she was treated with intravenous immunoglobulin with post-treatment platelet improvement to 53 × 10³/µL. She was discharged on a prednisone taper with plans for scheduled outpatient intravenous immunoglobulin and close follow-up in a combined hematology and maternal-fetal medicine clinic. This case highlights the importance of a structured, multidisciplinary approach to severe thrombocytopenia in pregnancy and the need to exclude pregnancy-specific and life-threatening alternative etiologies before confirming immune thrombocytopenia.

Indexed as

corticosteroidsimmune thrombocytopeniaintravenous immunoglobulinmaternal-fetal medicinepregnancythrombocytopenia

Identifiers

PMID42622037
PMCPMC13488538

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