Evidence map›Paper›PMID 28755615›Full record

ArticleInternational journal of surgery case reports2017

Abdominal leiomyosarcomatosis after surgery with external morcellation for occult smooth muscle tumors of uncertain malignant potential: A case report.

Antonio Macciò, Giacomo Chiappe, Paraskevas Kotsonis, Fabrizio Lavra, Michele Serra, Roberto Demontis, Clelia Madeddu

Open access · goldAbstract read
In one paragraph

Article in International journal of surgery case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Leiomyosarcoma Occurring After Hysterectomy for Benign Fibroids: A Case Report.Journal of obstetrics and gynaecology of India · 2022
    Article
  4. Review
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Antonio MacciòDepartment of Gynecologic Oncology, A. Businco Hospital, Azienda Ospedaliera Brotzu, via Jenner, 09100, Cagliari, Italy. Electronic address: a.maccio@tin.it.
Giacomo ChiappeDepartment of Gynecologic Oncology, A. Businco Hospital, Azienda Ospedaliera Brotzu, via Jenner, 09100, Cagliari, Italy.
Paraskevas KotsonisDepartment of Gynecologic Oncology, A. Businco Hospital, Azienda Ospedaliera Brotzu, via Jenner, 09100, Cagliari, Italy.
Fabrizio LavraDepartment of Gynecologic Oncology, A. Businco Hospital, Azienda Ospedaliera Brotzu, via Jenner, 09100, Cagliari, Italy.
Michele SerraDepartment of Gynecologic Oncology, A. Businco Hospital, Azienda Ospedaliera Brotzu, via Jenner, 09100, Cagliari, Italy.
Roberto DemontisDepartment of Public Health and Medical Sciences, University of Cagliari, 09042 Monserrato, Cagliari, Italy.
Clelia MadedduDepartment of Public Health and Medical Sciences, University of Cagliari, 09042 Monserrato, Cagliari, Italy.
Azienda Ospedaliera G. Brotzu · ITUniversity of Cagliari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAlthough rare, cases of abdominal sarcomatosis (AS) after laparotomy/laparoscopic interventions for uterine smooth muscle tumors of uncertain malignant potential (STUMP) have been reported. PRESENTATION OF CASE: We describe a rare case of diffuse abdominal sarcomatosis in a patient that some year earlier had undergone myomectomy for a suspected uterine myoma, which was histologically proven to be a STUMP. Once the patient was admitted at our Department, she underwent a diagnostic laparoscopy that confirmed a condition of peritoneal sarcomatosis disseminated through the entire abdomen, and then a laparotomic total hysterectomy, bilateral salpingo-oophorectomy, and total omentectomy, achieving a complete cytoreduction. Histological examination showed high-grade uterine leyomiosarcoma (LMS). Since there is no evidence of any clinical benefit of adjuvant treatment, given the risk of disease recurrence, we decided, with the patient's agreement, to conduct close follow-up with a Positron Emission Tomography (PET)/Computed Tomography (CT) scan every 3months and diagnostic laparoscopy every 6months, even in the absence of PET/CT positivity. After 2years PET/CT showed a relapse of LMS in the perigastric region and, therefore the patient underwent a diagnostic/operative laparoscopy with complete removal of the neoplastic recurrence. To date, the patient is disease-free. DISCUSSION AND

conclusionSTUMPs should be submitted to a frequent surveillance for their risk of recurrence, dissemination and transformation into LMS, even many years after the first diagnosis. A follow-up including surgical re-exploration with laparoscopy and PET/CT imaging may allow early detection and timely treatment of the relapse with good long-term outcome, as demonstrated by our case.

Indexed as

Abdominal sarcomatosisCase reportLaparoscopyLeiomyosarcomaUterine STUMP

Identifiers

PMID28755615
PMCPMC5537390
OpenAlexW2738678792

What OpenQuestion holds

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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.