ArticleClinical case reports2025
A Rare Clinical Presentation of Congenital Superficial Angiomyxoma: A Case Report.
Article in Clinical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- A Rare Clinical Presentation of Congenital Superficial Angiomyxoma: A Case Report.Clinical case reports · 2025Article
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Angiomyxoma is a rare atypical mesenchymal proliferation with two distinct forms, deep and superficial. Superficial Angiomyxoma tends to be benign with limited skin involvement. Rarely, Superficial Angiomyxoma appears in the vulvar region in the form of cystic, vascular, or tumoral lesions. The onset of vulvar superficial angiomyxoma is variable and ranges from early childhood to the post-menopausal period. To the best of our knowledge, this report presents the third documented case of vulvar superficial angiomyxoma with an onset at birth and a subsequent gradual increase in size over 2 years.
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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.