Evidence map›Paper›PMID 23777285›Full record

ArticleWorld journal of surgical oncology2013

Ovarian granulosa cell tumors: a retrospective study of 27 cases and a review of the literature.

Sakina Sekkate, Mouna Kairouani, Badr Serji, Adnane Tazi, Hind Mrabti, Saber Boutayeb, Hassan Errihani

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman.The Journal of clinical endocrinology and metabolism · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Postmenopausal Hyperandrogenism: Evaluation and Treatment Strategies.Endocrinology and metabolism clinics of North America · 2021
    Review
  10. Retrospective Analysis of 32 Cases of Ovarian Granulosa Cell Tumours.Journal of obstetrics and gynaecology of India · 2020
    Article
  11. Article
  12. Article
  13. 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

7 authors at 2 institutions in 1 country.

Sakina SekkateDepartment of Clinical Oncology, National Institute of Oncology, Rabat, Morocco. sakina.sekkate@yahoo.fr
Mouna Kairouani
Badr Serji
Adnane Tazi
Hind Mrabti
Saber Boutayeb
Hassan Errihani
Institut National d'Oncologie · MACentre Hospitalier Ibn Sina · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGranulosa tumors were described for the first time in 1855 by Rokitansky. These tumors are malignancies with a relatively favorable prognosis. They are characterized by a prolonged natural history and a tendency to late recurrences. The aim of this study is to investigate the epidemiological and pathological characteristics of granulosa cell tumors and to investigate the prognosis factor for recurrences.

methodsThe clinical data of patients who were treated in the period from January 2003 to December 2010 at the National Institute of Oncology in Rabat, Morocco for adult granulosa cell tumors of the ovary were investigated retrospectively. Data for age, clinical manifestation, imaging, diagnosis and treatment of the patients were reviewed and analyzed. Post-operative histology was obtained for all patients.

resultsTwenty-seven cases were retrieved. The median patient age was 53 years. The most common clinical manifestations at diagnosis were abdominal pain and vaginal bleeding. Mean tumor size was 14 cm. The majority of patients had stage I (63%, n = 17), while (18,5%, n = 5) had stage III, (7.4%, n = 2) had stage IV, and (11%, n = 3) of patients had an unknown stage. In the follow-up period (median = 63.44 months), five (18.51%) patients relapsed. The median time to relapse was 41.8 months, (range: 18 to 62 months).

conclusionsGranulosa cell tumor of the ovary is an uncommon neoplasm. The adult form progresses slowly and often is diagnosed in an early stage of disease. Surgery is indicated. A prolonged post-therapeutic follow-up is necessary because of the risk of recurrences, late and exceptional for the adult form.

Indexed as

AdultAgedCombined Modality TherapyFemaleFollow-Up StudiesGranulosa Cell TumorHumansMaleMiddle AgedMoroccoNeoplasm Recurrence, LocalNeoplasm StagingOvarian NeoplasmsPrognosisRetrospective StudiesSurvival Rate

Identifiers

PMID23777285
PMCPMC3691822
OpenAlexW2170207827

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Registered trials

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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.