Evidence map›Paper›PMID 41649706›Full record

ArticleClinical and experimental nephrology2026

Incidence and clinicopathological analysis of portal vein and inferior vena cava thrombosis in autopsy cases of autosomal dominant polycystic kidney disease.

Anna Shinozaki, Tomoko Yamamoto, Atsushi Kurata

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Article in Clinical and experimental nephrology, 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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3 authors.

Anna ShinozakiTokyo Women's Medical University, Tokyo, Japan.
Tomoko YamamotoDepartment of Pathology, Tokyo Women's Medical University, 8-1 Kawada-Cho, Shinjuku-Ku, Tokyo, 162-8666, Japan.
Atsushi KurataDepartment of Pathology, Tokyo Women's Medical University, 8-1 Kawada-Cho, Shinjuku-Ku, Tokyo, 162-8666, Japan. kurata.atsushi@twmu.ac.jp.

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6 · The paper itself

Abstract

backgroundWith regard to complications of portal vein (PV) and inferior vena cava (IVC) thrombosis in autosomal dominant polycystic kidney disease (ADPKD), several cases have been reported based on imaging findings. However, only one autopsy case has been described and no systematic analysis has been conducted to date. This retrospective study aimed to review autopsy cases from our department over the past 37 years to clarify the frequency and background factors of thrombosis formation in ADPKD.

methodsAmong 4001 autopsies performed at our institution from 1987 to 2023, 10 ADPKD cases were identified. We examined the presence of thrombus in these 10 cases and compared pleural effusion and ascites volumes, major organ weights, and clinicopathological factors between cases with thrombus and those without.

resultsAmong 10 ADPKD cases, thrombi were identified in four cases in which autopsies were performed relatively recently. These thrombi were distributed in the PV, IVC, and their branches. Compared to non-thrombotic cases, those with thrombi showed a statistically significant increase in kidney weight and tended to have a higher frequency of complications such as sepsis and severe aortic atherosclerosis.

conclusionThis study reports the first systematic autopsy-based investigation of PV and IVC thrombosis in ADPKD. Thrombosis was found at a high frequency of 40% and appears to have increased in recent years. Increased kidney weight was associated with thrombosis formation, and blood stasis due to compression by enlarged kidneys is considered the primary cause. Further case accumulation and elucidation of the pathophysiology involved are anticipated.

Indexed as

Polycystic Kidney, Autosomal DominantPortal VeinVena Cava, InferiorVenous ThrombosisAdultAgedAutopsyFemaleHumansIncidenceKidneyMaleMiddle AgedOrgan SizeRetrospective StudiesAutopsyAutosomal dominant polycystic kidney diseaseInferior vena cavaPortal veinThrombus

Identifiers

PMID41649706
PMCPMC13090223

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