Evidence map›Paper›PMID 42491834›Full record

ArticleCytoJournal2026

Myxoid spindle cell lipoma of the ileum: Clinicopathological features and diagnostic insights.

Ruirui Fan, Jie Gao

Abstract read
In one paragraph

Article in CytoJournal, 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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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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ruirui FanDepartment of Anatomical Pathology, The Islands Healthcare Complex-Macao Medical Center of Peking Union Medical College Hospital, Macao, China.
Jie GaoDepartment of Pathology, Xiamen Humanity Hospital, Xiamen, Fujian, China.ORCID https://orcid.org/0009-0003-4086-5076

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study analyzes a rare myxoid spindle cell lipoma (SCL) around the ileum. It aims to systematically summarize the clinicopathological features of this tumor at an atypical location. This will improve understanding of this rare condition. Material and Methods: We conducted a detailed study of SCL around the ileum. This mass was incidentally found in a right hemicolectomy specimen. The analysis integrated multiple methods. These included histomorphological observation, immunohistochemical staining, and molecular testing. Results: The tumor showed a typical myxoid stromal background. It contained spindle cells and scattered mature adipocytes. The characteristic thick collagen bundles commonly seen in classic SCL were absent. A diagnosis of myxoid SCL was confirmed based on the following features: CD34-positive spindle cells, loss of retinoblastoma protein 1expression, a low Ki-67 index, and the absence of MDM2 amplification by both IHC and fluorescence in situ hybridization. This profile effectively excludes malignant differential diagnoses, such as liposarcoma. Conclusion: Myxoid SCL around the ileum is extremely rare. Its diagnosis relies on recognizing its characteristic morphological spectrum. Immunohistochemistry and molecular testing are essential to exclude malignant tumors. A comprehensive understanding of its unique presentation at atypical sites is crucial. This is important for achieving accurate diagnosis and preventing inappropriate treatment.

Indexed as

Diagnosis and differential diagnosisHistopathologyIleumSpindle cell lipoma

Identifiers

PMID42491834
PMCPMC13378979

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.