Evidence map›Paper›PMID 41808950›Full record

ArticleCirculation reports2026

Long-Term Outcomes of Primary Cardiac Tumors by Histological Subtype.

Mikio Shiba, Masayuki Nishiyama, Yohei Sotomi, Yuichi Motoyama, Yasuhiro Ichibori, Masatoshi Hata, Yoshiharu Higuchi

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Article in Circulation reports, 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Mikio ShibaCardiovascular Division, Hyogo Prefectural Nishinomiya Hospital Hyogo Japan.
Masayuki NishiyamaDepartment of Cardiovascular Surgery, Osaka Keisatsu Hospital Osaka Japan.
Yohei SotomiCardiovascular Division, Osaka Keisatsu Hospital Osaka Japan.
Yuichi MotoyamaDepartment of Diagnostic Pathology, Osaka Keisatsu Hospital Osaka Japan.
Yasuhiro IchiboriCardiovascular Division, Osaka Keisatsu Hospital Osaka Japan.
Masatoshi HataDepartment of Cardiovascular Surgery, Osaka Keisatsu Hospital Osaka Japan.
Yoshiharu HiguchiCardiovascular Division, Hyogo Prefectural Nishinomiya Hospital Hyogo Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Primary cardiac tumors are rare, and the prognostic impact of their histological subtypes remains poorly understood. We assessed the clinical outcomes of benign and malignant tumors using long-term follow-up data from pathologically confirmed cases. Methods and Results: We retrospectively analyzed 42 consecutive patients diagnosed with primary cardiac tumors between 2007 and 2022 at a single center. Among them, 41 patients who underwent surgical resection were followed longitudinally and included in the present study. Clinical features, tumor distribution, and outcomes were assessed by histological type, with particular focus on long-term prognosis. Histological diagnoses were confirmed in each case. Myxomas accounted for 73% (n=30), diffuse large B-cell lymphomas (DLBCLs) for 7% (n=3), and other benign tumors for 20% (n=8) of cases. Myxomas were predominantly located in the left atrium and showed excellent long-term outcomes, with no recurrence or tumor-related deaths over a median follow-up of 12.8 years. In contrast, all patients with DLBCL had right-sided tumors and died within 2 years due to disease progression despite surgery and chemotherapy. Kaplan-Meier analysis showed significant differences (P<0.001) in survival among tumor types, with DLBCL showing uniformly poor outcomes. Conclusions: Benign cardiac tumors had favorable outcomes, with myxomas showing a particularly excellent prognosis. In contrast, malignant tumors were uniformly associated with early death. Histological subtype may be associated with survival.

Indexed as

Cardiac tumorDiffuse large B-cell lymphoma (DLBCL)MalignancyMyxomaPrognosis

Identifiers

PMID41808950
PMCPMC12971211

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