Evidence map›Paper›PMID 35702134›Full record

ArticleAmerican journal of translational research2022

Clinicopathologic and molecular features of vascular tumors in a series of 118 cases.

Huiting Wei, Tiantian Zhen, Ying Tuo, Hui Li, Jiangtao Liang, Shaoyu Chen, Huijuan Shi, Anjia Han

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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 2 institutions in 1 country.

Huiting WeiDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Tiantian ZhenDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Ying TuoDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Hui LiDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Jiangtao LiangDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Shaoyu ChenGuangzhou LBP Medical Technology Co., Ltd. Guangzhou, China.
Huijuan ShiDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Anjia HanDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University Guangzhou, China.
Sun Yat-sen University · CNGuangzhou Electronic Technology (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsVascular tumors are composed of benign, intermediate, and malignant lesions. The diagnosis is challenging because some entities demonstrate overlapping morphologies and harbor the same genetic alterations. We describe herein a cohort of vascular tumors with clinicopathologic, immunohistochemical, and molecular features. METHODS AND

results118 vascular tumors including 56 angiosarcomas, 18 epithelioid haemangioendotheliomas (EHE), 25 epithelioid haemangiomas (EH), 8 pseudomyogenic haemangioendotheliomas (PHE), 1 papillary intralymphatic angioendothelioma (PILA), 2 kaposiform haemangioendotheliomas (KHE), 3 Kaposi sarcomas, 2 retiform haemangioendotheliomas (RHE), and 3 anastomosing haemangiomas were assessed. FOSB, c-Fos, CAMTA1, and TFE3 expression and gene rearrangements were analyzed by immunohistochemical staining and FISH, respectively. Our results showed that FOSB expression was diffusely positive in all 8 PHEs, focally or sparsely in 12 EHs, and in 2 angiosarcomas. C-FOS expression was sparsely to diffusely positive in 15 EHs, focally or sparsely in 17 angiosarcomas, 1 EHE, 1 Kaposi sarcoma, and 1 PHE. CAMTA1 expression was positive in only 12 EHEs. TFE3 expression was focally or sparsely positive in all 8 PHEs, 22 angiosarcomas, 6 EHEs, 3 EHs, 2 Kaposi sarcomas, and 2 AHs.

conclusionsFOSB and CAMTA1 are useful diagnostic markers for PHE and EHE, respectively.

Indexed as

CAMTA1c-FOSfluorescence in situ hybridizationFOSBTFE3Vascular tumors

Identifiers

PMID35702134
PMCPMC9185040
OpenAlexW4285740385

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.