ArticleCureus2025
Idiopathic Scrotal Calcinosis (ISC): A Familial Case Series of Two Cases.
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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0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Idiopathic scrotal calcinosis (ISC) is a rare condition characterized by the development of multiple, asymptomatic, painless nodules on the scrotal skin. While typically considered idiopathic, its etiology remains unclear, with potential links to the dystrophic calcification of pre-existing lesions. We present a familial case series of father and son with ISC, highlighting the clinical presentation, surgical management, and importance of histopathological confirmation.
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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.