Evidence map›Paper›PMID 31934089›Full record

ArticleInternational journal of clinical and experimental pathology2019

Spindle cell lipoma: clinicopathologic characterization of 40 cases.

Shuai Chen, Haining Huang, Shujin He, Wei Wang, Ran Zhao, Lei Li, Zhihong Cui, Renya Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. A case report unveiling spindle cell lipoma.Radiology case reports · 2025
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  9. A case report of spindle cell lipoma.Annals of medicine and surgery (2012) · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Esophageal spindle cell lipoma.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
  14. Review
  15. Review
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

8 authors at 3 institutions in 1 country.

Shuai ChenDepartment of Pathology, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Haining HuangDepartment of Pharmacy, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Shujin HeClinical College, Jining Medical University Jining, Shandong Province, P. R. China.
Wei WangDepartment of Pathology, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Ran ZhaoDepartment of Pathology, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Lei LiDepartment of Pathology, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Zhihong CuiDepartment of Pathology, The Second People's Hospital of Jining Jining, Shandong Province, P. R. China.
Renya ZhangDepartment of Pathology, Affiliated Hospital of Jining Medical University Jining, Shandong Province, P. R. China.
Affiliated Hospital of Jining Medical University · CNJining First People's Hospital · CNJining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn view of the existence of multifarious pathologic subtypes of spindle cell lipoma (SCL), which is easily misdiagnosed as other benign and malignant soft tissue tumors, we performed this study and aimed to better define the category of SCL.

methodsWe collected and analyzed 40 cases of SCL with complete clinical and pathologic information from January 2010 to December 2018. Clinical and histopathologic analyses of SCL were performed, as well as immunohistochemical staining and fluorescence in situ hybridization (FISH) using probes for

resultsIn 40 cases, the male to female ratio was 3.4:1, and the mean age was 54 years old. SCL of our study included six pathologic subtypes: classic (25/40), fibrous (4/40), myxoid (4/40), low-fat (3/40), pseudoangiomatous (2/40), and fat-rich (2/40) changes. Microscopically, SCL showed distinctive morphology, with uniform spindle cells and a variably adipocytic component. The spindle cells were bland in morphology, without prominent atypia or pleomorphism, set in a myxoid or fibrous matrix. Immunohistochemically, CD34 and vimentin were positive in spindle cells, and spindle cells of 6 cases also expressed S-100 protein. FISH analysis of 10 cases revealed that heterozygous deletion of

conclusionsSCL is a rare benign lipoma, and the proportion of spindle cells and adipocytic component varies, which may form various pathologic changes. The diagnosis needs to be combined with clinicopathologic features, immunophenotypes, and genetics. It has to be differentiated from mammary-type myofibroblastoma, cellular angiolipoma, solitary fibrous tumor, and myxoid liposarcoma.

Indexed as

differential diagnosisMDM2RB1S-100Spindle cell lipoma (SCL)

Identifiers

PMID31934089
PMCPMC6949558
OpenAlexW3005757377

What OpenQuestion holds

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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.