ArticleCureus2025
Kasabach-Merritt Syndrome in Neonates: A Case of Complexity and Care.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Kasabach-Merritt syndrome (KMS) is a rare and potentially life-threatening pediatric coagulopathy characterized by thrombocytopenia, microangiopathic hemolytic anemia, and coagulation abnormalities. Clinically, it presents as a reddish-purple mass resembling a hemangioma. Diagnosis relies on a combination of clinical and biological assessments, sometimes supplemented by biopsy to confirm the hemangioma. We present the case of a one-day-old male neonate with an angioma affecting the right hemothorax and upper limb, accompanied by thrombocytopenia. The patient responded favorably to treatment with corticosteroids, chemotherapy, and aspirin. Therapeutic strategies were carefully evaluated and discussed.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.