Evidence map›Paper›PMID 38028045›Full record

ArticleClinical case reports2023

A needle in the haystack: An unusual case presentation of ganglioneuroblastoma at a tertiary care center in Coastal Karnataka.

Shalini Radhakrishnan, Ranjitha Rao, Harsha Prasada Lashkari, Hema Kini, Jyoti Ramnath Kini, Vatsala Basavaraju Kudurugundi, Vanishree Ashok, Chaithra Venkataramana Gowthuvalli

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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.

Shalini RadhakrishnanDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0009-0002-3407-6030
Ranjitha RaoDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0001-9786-0485
Harsha Prasada LashkariDepartment of Paediatric Haematology and Oncology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0002-6398-6546
Hema KiniDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0003-0803-6692
Jyoti Ramnath KiniDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0002-3351-9517
Vatsala Basavaraju KudurugundiDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0002-8926-9289
Vanishree AshokKasturba Medical College Mangalore, Jyothi Circle Mangalore India.
Chaithra Venkataramana GowthuvalliDepartment of Pathology Kasturba Medical College Mangalore, Manipal Academy of Higher Education Manipal India.ORCID https://orcid.org/0000-0002-5906-5197
Manipal Academy of Higher Education · INKasturba Medical College, Mangalore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Key Clinical Message: This case report highlights the importance of recognizing and accurately diagnosing ganglioneuroblastoma, an uncommon variant of neuroblastic tumors in children. Ganglioneuroblastomas have diverse clinical and morphological presentations, and histopathological examination is paramount in guiding treatment decisions, especially in cases with ambiguous symptoms. Early detection is crucial, as the prognosis varies significantly based on the subtype and the presence of metastatic disease. Clinicians should maintain a high index of suspicion and utilize radiological examinations to promptly identify and treat these tumors. Abstract: Children are frequently affected by neuroblastic tumors, which grow from the sympathoadrenal lineage of the neural crest during its development. However, intermixed ganglioneuroblastomas are far less common within the same tumor spectrum, the diagnosis of which could become challenging amidst an unusual presentation. In our case report, we present a 4-year-old boy who had complaints of fever and difficulty in walking, with a supra-renal mass on ultrasound, which was diagnosed as ganglioneuroblastoma-intermixed type on histopathological examination. This report aims to contribute to the understanding of the diverse clinical and morphological spectrum of ganglioneuroblastomas and the importance of multidisciplinary collaboration and histopathological examination to enhance decision-making in such ambiguous scenarios.

Indexed as

atypical presentationcase reportsganglioneuroblastomahistopathological examinationmorphological diversityneuroblastic tumors

Identifiers

PMID38028045
PMCPMC10665580
OpenAlexW4388947888

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.