Evidence map›Paper›PMID 42254984›Full record

ArticleOpen medicine (Warsaw, Poland)2026

Development of a clinical nomogram for predicting hemorrhagic rupture in renal angiomyolipoma and analysis of molecular correlates (

Xiaobing Li, Jie Wan, Xuemei Li, Yao Zhang, Xianhui Hu

Abstract read
In one paragraph

Article in Open medicine (Warsaw, Poland), 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaobing LiScience and Technology Industry Development Center, Chongqing Medical and Pharmaceutical College, Chongqing, China.ORCID https://orcid.org/0009-0005-3723-9626
Jie WanSpecial Medical Department, Daping Hospital, Army Medical University, Chongqing, China.
Xuemei LiScience and Technology Industry Development Center, Chongqing Medical and Pharmaceutical College, Chongqing, China.
Yao ZhangDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xianhui HuUrology Department, Chengdu Integrated TCM & Western Medicine Hospital, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Hemorrhagic rupture is a severe and potentially life-threatening complication of renal angiomyolipoma (AML). However, current clinical tools for accurately predicting hemorrhage risk remain limited. This study aimed to establish and validate a clinical nomogram for predicting hemorrhagic rupture in AML based on preoperative characteristics, and to investigate the underlying molecular correlates involving Methods: A total of 379 patients with AML and 40 normal kidney tissue samples (2010-2021) were retrospectively analyzed. Patients were temporally divided into a training cohort (n=285) and an independent temporal validation cohort (n=94). Independent clinical predictors of hemorrhagic rupture were identified through univariate and multivariate logistic regression and incorporated into a nomogram. Model performance was evaluated using receiver operating characteristic (ROC) analysis and calibration plots in the validation cohort. Additionally, immunohistochemistry, qPCR, and ELISA were conducted to assess Results: Tuberous sclerosis complex (TSC), tumor size ≥4 cm, rich vascular supply, and exophytic growth pattern were identified as independent predictors of hemorrhagic rupture (all p<0.05). The nomogram demonstrated excellent discrimination (AUC=0.967) and satisfactory calibration in the independent validation cohort. At the molecular level, immunohistochemical analysis revealed elevated Conclusions: The developed nomogram serves as a reliable pre-operative tool for individualized risk stratification of AML rupture. Furthermore, the aberrant expression of

Indexed as

CD34hemorrhagic rupturenomogramPPARGPTENrenal angiomyolipoma (AML)

Identifiers

PMID42254984
PMCPMC13238147

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