Evidence map›Paper›PMID 37814748›Full record

ArticleCureus2023

An Aberrant Case of Pheochromocytoma in a Young Adult Presenting With Secondary Hypertension: A Case Report With Review of the Literature.

Deepali Trimukhe, Avinash Dhok, Suresh Phatak, Prashant Onkar

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 74% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Deepali TrimukheRadiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre (NKPSIMS & RC) and Lata Mangeshkar Hospital (LMH), Nagpur, IND.
Avinash DhokRadiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre (NKPSIMS & RC) and Lata Mangeshkar Hospital (LMH), Nagpur, IND.
Suresh PhatakRadiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre (NKPSIMS & RC) and Lata Mangeshkar Hospital (LMH), Nagpur, IND.
Prashant OnkarRadiodiagnosis, NKP Salve Institute of Medical Sciences and Research Centre (NKPSIMS & RC) and Lata Mangeshkar Hospital (LMH), Nagpur, IND.
NKP Salve Institute of Medical Sciences and Lata Mangeshkar Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pheochromocytoma (PCC) is a rare neuroendocrine catecholamine-secreting tumour of the adrenal gland. It originates from the chromaffin cells found within the adrenal medulla or the extra-adrenal paraganglia. We present a case report of a 24-year-old female who presented with hypertension, headache, palpitations, chest pain and blurry vision. On ultrasound evaluation, a right suprarenal mass was noted, which was further evaluated using contrast-enhanced computed tomography (CT). Based on our imaging findings, the patient was diagnosed with a case of right-sided pheochromocytoma. The patient was operated on, and our diagnosis was confirmed with histopathological examination.

Indexed as

adrenal paragangliomacatecholamine-secreting tumourlight bulb appearanceneuroendocrine tumourpheochromocytomayoung hypertensive

Identifiers

PMID37814748
PMCPMC10560397
OpenAlexW4386543188

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.