Evidence map›Paper›PMID 33161462›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Atypical nodular fasciitis with a novel PAFAH1B1-USP6 fusion in a 22-month-old boy.

Yan Qiu, Ran Peng, Huijiao Chen, Hua Zhuang, Xin He, Hongying Zhang

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Frontiers in oncology · 2022
    Article
  9. Morphologically malignant nodular fasciitis with CALD1-USP6 fusion.Virchows Archiv : an international journal of pathology · 2021
    Article
  10. Ubiquitin-specific Peptidase 6 (Cancer genomics & proteomics
    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

6 authors at 1 institution in 1 country.

Yan QiuDepartment of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.
Ran PengDepartment of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.
Huijiao ChenDepartment of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.
Hua ZhuangDepartment of Ultrasound, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Xin HeDepartment of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China.
Hongying ZhangDepartment of Pathology, West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, 610041, Sichuan, China. hy_zhang@scu.edu.cn.ORCID http://orcid.org/0000-0003-4748-4121
Sichuan University · CN

Funding

135 Project for Disciplines of Excellence-Clinical Research Incubation Project No. 2018HXFH011National Natural Science Foundation of China 81472510National Natural Science Foundation of China 81972520Sichuan Science and Technology Program 2020YFS0270
6 · The paper itself

Abstract

Nodular fasciitis (NF) rarely occurs in infants aged < 2 years although cranial fasciitis develops predominantly in this age group. Histologically, NF may present high cellularity and brisk mitoses, but atypical forms are generally absent. Here, we report a NF in a 22-month-old Chinese boy. Microscopically, the lesion was manifested as cellular variant of NF. Notably, atypical mitotic figures including multipolar form were identified. Immunohistochemically, the neoplastic cells showed strong positivity for smooth muscle actin. Fluorescence in situ hybridization analysis revealed an unbalanced rearrangement of USP6, along with the USP6 increased copies. Subsequent next-generation sequencing-based technology revealed a novel PAFAH1B1-USP6 fusion gene as well as unusual fusion point on USP6 (exon 9). To the best of our knowledge, this is the only reported case with overt atypical mitosis. This case is also the first published example of genetically confirmed infant NF. Additionally, PAFAH1B1-USP6 fusion has never been described in NF.

Indexed as

Gene Fusion1-Alkyl-2-acetylglycerophosphocholine EsteraseFasciitisGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingHumansInfantIn Situ Hybridization, FluorescenceMaleMicrotubule-Associated ProteinsMitosisPhenotypeUbiquitin Thiolesterase1-Alkyl-2-acetylglycerophosphocholine EsteraseMicrotubule-Associated ProteinsPAFAH1B1 protein, humanUbiquitin ThiolesteraseUSP6 protein, humanAtypical mitosesNodular fasciitisPAFAH1B1-USP6 fusionPediatricUnbalanced rearrangement

Identifiers

PMID33161462
OpenAlexW3095342550

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.