Evidence map›Paper›PMID 38031835›Full record

ReviewPediatric endocrinology, diabetes, and metabolism2023

Adrenocortical carcinoma - 12-year observation period in a single centre. Case report with literature review.

Patrycja Dasiewicz, Elżbieta Moszczyńska, Danuta Perek, Dariusz Polnik, Maria Stepaniuk, Joanna Trubicka, Wiesława Grajkowska

Open access · diamondAbstract readReviewCase Reports
In one paragraph

Review in Pediatric endocrinology, diabetes, and metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Adrenal cortical carcinoma: Paediatric aspects - literature review.Pediatric endocrinology, diabetes, and metabolism · 2024
    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 1 institution in 1 country.

Patrycja DasiewiczDepartment of Endocrinology, Children's Memorial Health Institute, Warsaw, Poland.
Elżbieta MoszczyńskaDepartment of Endocrinology, Children's Memorial Health Institute, Warsaw, Poland.
Danuta PerekDepartment of Oncology, Children's Memorial Health Institute, Warsaw, Poland.
Dariusz PolnikDepartment of Surgery, Children's Memorial Health Institute, Warsaw, Poland.
Maria StepaniukDepartment of Pathology, Children's Memorial Health Institute, Warsaw, Poland.
Joanna TrubickaDepartment of Pathology, Children's Memorial Health Institute, Warsaw, Poland.
Wiesława Grajkowska
Children's Memorial Health Institute · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdrenocortical carcinoma (ACC) accounts for 0.2% of childhood malignancies. The most common symptom in children is rapidly progressive androgenization. Herein, we report a case of a patient with symptoms of hypercortisolaemia and androgenization, who was diagnosed with ACC. CASE PRESENTATION: In a 10-year-old patient with ACC the course of the disease was complicated by 3 recurrences. She was treated with surgery, chemo-, and radiotherapy. Currently, 8 years after the end of treatment, there have been no signs of recurrence.

conclusionsA patient after ACC treatment requires regular check-ups and long-term observation. Constant supervision enables early diagnosis of disease recurrence, and the use of treatment improves the prognosis.

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaChildFemaleHumansVirilismadrenocortical carcinomaadrenocortical tumourmitotan.

Identifiers

PMID38031835
PMCPMC10679906
OpenAlexW4388669322

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.