Rare rectal elastofibroma: diagnostic challenges and case report
- PMID: 40388002
- PMCID: PMC12089562
- DOI: 10.1007/s12672-025-02556-6
Rare rectal elastofibroma: diagnostic challenges and case report
Abstract
Elastofibroma (EF) is a rare soft tissue tumor that typically occurs in the scapular region, with its occurrence in the rectum being extremely uncommon. In this report, we present a case of rectal EF in a 72-year-old female, which was definitively diagnosed through histopathology, immunohistochemistry, and special staining analyses. This case emphasizes the diagnostic challenges posed by rectal EF and underscores the necessity of histopathological and immunohistochemical assessment in distinguishing it from other spindle cell neoplasms, particularly when imaging findings are inconclusive.
Keywords: Case report; Elastofibroma; Neuroendocrine tumors; Rectum; Special staining.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: The research was ethically approved by Guizhou Medical University. Prior to participation, participants were duly informed of her rights and responsibilities and provided explicit written consent. The study was conducted in agreement with the guidelines governing research involving human participants, as outlined by the Ethics Committee of Guizhou Medical University. Consent to publication: The authors have obtained written consent to publish the images/details of the individual(s) included in this manuscript. Competing interests: The authors declare no competing interests.
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