Evidence map›Paper›PMID 32698283›Full record

ArticleInternational journal of surgery case reports2020

Endometrial stromal sarcoma arising from polypoid endometriosis: Case report and literature review.

Fabio Carbone, Manou Manpreet Kaur, Aik Yong Chok, Christos Kontovounisios, Thomas Ind, Shahnawaz Rasheed

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Update on Endometrial Stromal Tumours of the Uterus.Diagnostics (Basel, Switzerland) · 2021
    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 2 institutions in 2 countries.

Fabio CarboneDepartment of Colorectal Surgery, The Royal Marsden Hospital, London, UK; Department of Advanced Biomedical Sciences, Università Degli Studi Di Napoli "Federico II", Napoli, Italy. Electronic address: fa.carbone87@gmail.com.
Manou Manpreet KaurDepartment of Gynaecological Oncology, The Royal Marsden Hospital, London, UK. Electronic address: manou.m.kaur@gmail.com.
Aik Yong ChokDepartment of Colorectal Surgery, The Royal Marsden Hospital, London, UK. Electronic address: chokaikyong@gmail.com.
Christos KontovounisiosDepartment of Colorectal Surgery, The Royal Marsden Hospital, London, UK; Departments of Surgery and Cancer, Imperial College, London, UK; Department of Colorectal Surgery, Chelsea and Westminster Hospital, London, UK. Electronic address: c.kontovounisios@imperial.ac.uk.
Thomas IndDepartment of Gynaecological Oncology, The Royal Marsden Hospital, London, UK. Electronic address: thomasind@me.com.
Shahnawaz RasheedDepartment of Colorectal Surgery, The Royal Marsden Hospital, London, UK. Electronic address: shahnawaz.rasheed@rmh.nhs.uk.
Royal Marsden Hospital · GBUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolypoid endometriosis (PE) is a rare and uncommon variant of endometriosis that may present as a polypoid mass that simulates a malignant neoplasm. Typically, PE develops locally as a large benign pelvic mass. However, it may sometimes conceal a malignant disease in its context. CASE PRESENTATION: A 53 years old, nulliparous lady, had been treated over a 10-year period for recurrent and symptomatic polypoid endometriosis of the pelvis. During this time, she underwent four surgical resections, the final one being a total pelvic exenteration, with histology demonstrating the presence of a rare myxoid low grade Endometrial Stromal Sarcoma (ESS) that had arisen in PE.

conclusionPE is a rare variant growth pattern of endometriosis which may involve different pelvic organs and can mimic a malignant mass in the pelvis. It mostly affects women in their peri- or post-menopausal age and it is not always related to hormonal therapy. Malignances, such as Endometrial Stromal Sarcoma in this case, can arise in the context of PE and their diagnosis can be challenging. Surgical excision may constitute radical multi-organ resection, particularly for recurrent and symptomatic cases. However, the recurrence rates after surgery can be significant.

Indexed as

Endometrial stromal sarcomaEndometriosisPelvic massPolypoid endometriosisSurgeryTotal pelvic exenteration

Identifiers

PMID32698283
PMCPMC7327825
OpenAlexW3036041073

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.