Evidence map›Paper›PMID 41458523›Full record

ArticleFrontiers in medicine2025

Dendritic fibromyxolipoma of the male breast: case report and literary review.

Xiaolan Li, Demian Wu, Xiaoxue Tian, Ting Xu, Qiyao Ge, Shuai Luo, Jinjing Wang

Abstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Xiaolan LiDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Demian WuDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Xiaoxue TianDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Ting XuDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Qiyao GeClinical Medicine, Guizhou Medical University, Guiyang, Guizhou, China.
Shuai LuoDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.
Jinjing WangDepartment of Pathology, Affiliated Hospital of Zunyi Medical University, Zunyi, Guizhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dendritic fibromyxolipoma (DFML) represents a benign lipomatous tumor. Its rarity and distinctive morphology can lead to misinterpretation of other mesenchymal malignancies, which may result in unnecessary aggressive treatments. Case presentation: A 39-year-old male presented with a left mammary mass that had been noticed 1 year earlier. Chest computed tomography identified a nodule characterized by fat density in the left mammary region. The initial clinical impression was gynecomastia. A local excision of the left mammary mass was subsequently performed. Histopathological analysis confirmed the diagnosis of DFML. Post-surgical follow-up over 38 months showed no recurrence. Conclusion: DFML is a benign lipomatous tumor with unique morphological features. Complete surgical excision typically leads to no recurrence. This report documents the first known instance of DFML in the mammary gland of a male patient. Furthermore, an analysis of 95 previously documented cases of DFML was conducted. It is strongly advocated that the World Health Organization reclassify DFML as a mucinous subtype of spindle cell lipoma. This reclassification would improve the understanding of DFML and help avoid unnecessary aggressive treatments due to misdiagnosis as a malignancy.

Indexed as

dendritic fibromyxolipomadifferential diagnosismammarypathological characteristicsreview

Identifiers

PMID41458523
PMCPMC12742310

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