Evidence map›Paper›PMID 35779129›Full record

ArticleMedical molecular morphology2022

Atypical spindle cell/pleomorphic lipomatous tumor with a sarcomatous component showing high mitotic activity and Ki-67 labeling index: report of a unique case mimicking dedifferentiated liposarcoma.

Shintaro Sugita, Taro Sugawara, Makoto Emori, Tomoyuki Aoyama, Michiko Hosaka, Keiko Segawa, Hiromi Fujita, Tadashi Hasegawa

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Medical molecular morphology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Atypical Spindle Cell/Pleomorphic Lipomatous Tumor With Sarcomatous Transformation: Clinicopathologic and Molecular Analysis of 4 Cases.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2024
    Article
  7. Article
  8. 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 1 institution in 1 country.

Shintaro SugitaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Taro SugawaraDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Makoto EmoriDepartment of Orthopedic Surgery, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Tomoyuki AoyamaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Michiko HosakaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Keiko SegawaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Hiromi FujitaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan.
Tadashi HasegawaDepartment of Surgical Pathology, School of Medicine, Sapporo Medical University, Sapporo, Hokkaido, 060-8543, Japan. hasetada@sapmed.ac.jp.
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atypical spindle cell/pleomorphic lipomatous tumor (ASPLT) is a new entity of benign adipocytic tumor that spans a wide spectrum of histology from adipocytic to spindle cell/pleomorphic tumors. The latter non-adipocytic component rarely shows sarcomatous features although ASPLTs are not thought to dedifferentiate. A 78-year-old woman with ASPLT in the left thigh had a sarcomatous component with high mitotic activity and Ki-67 labeling index (LI) mimicking dedifferentiated liposarcoma. The adipocytic component consisted of various-sized adipocytic cells with few lipoblasts. The sarcomatous component consisted of a fascicular proliferation of atypical spindle cells with scattered large bizarre and multinucleated giant cells. Mitotic figures including atypical mitoses were frequently observed. Immunohistochemically, the tumor cells were positive for cluster of differentiation 34 but not mouse double minute 2 homolog (MDM2), cyclin-dependent kinase 4 (CDK4), or retinoblastoma (Rb) protein. Ki-67 LI in the sarcomatous component reached 40%. MDM2 and CDK4 genes were not amplified and 13q14 including the RB1 locus was deleted according to fluorescence in situ hybridization. The patient is alive with no evidence of local recurrence or distant metastasis 3.5 years after surgery. As ASPLT may exhibit morphological variation, it is important to rule out dedifferentiated liposarcoma with careful pathological examination.

Indexed as

LipomaLiposarcomaAgedBiomarkers, TumorCyclin-Dependent Kinase 4FemaleHumansIn Situ Hybridization, FluorescenceKi-67 AntigenBiomarkers, TumorCyclin-Dependent Kinase 4Ki-67 AntigenAtypical spindle cell/pleomorphic lipomatous tumorCDK4Dedifferentiated liposarcomaFluorescence in situ hybridizationImmunohistochemistryMDM2

Identifiers

PMID35779129
OpenAlexW4283777613

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.