Evidence map›Paper›PMID 38022857›Full record

ArticleSAGE open medical case reports2023

Left anterior descending artery disease in a 27-year-old with multiple endocrine neoplasia, type 2A: A case report.

Mohammed Omar Al Salihi, Murali K Iyyani, Sarina Koilpillai, Gerson Quintero, Jorge Parellada, S J Carlan

Open access · goldAbstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 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 71% 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

6 authors at 1 institution in 1 country.

Mohammed Omar Al SalihiDepartment of Internal Medicine, Orlando Health, Orlando, Florida, USA.
Murali K IyyaniDepartment of Internal Medicine, Orlando Health, Orlando, Florida, USA.
Sarina KoilpillaiDepartment of Internal Medicine, Orlando Health, Orlando, Florida, USA.
Gerson QuinteroDepartment of Internal Medicine, Orlando Health, Orlando, Florida, USA.
Jorge ParelladaDepartment of Internal Medicine, Orlando Health, Orlando, Florida, USA.
S J CarlanDivision of Academic Affairs and Research, Orlando Health, Orlando, Florida, USA.ORCID https://orcid.org/0000-0001-9867-8538
Orlando Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple endocrine neoplasia 2A is an autosomal dominant disease characterized by medullary thyroid cancer, pheochromocytoma, and primary hyperparathyroidism. Coronary artery disease is associated with the disorder, but the mechanism is unclear. A 27-year-old female presented with chest pain and palpitations. A left heart catheterization was performed and showed 80% stenosis of the left anterior descending artery. Imaging and workup also revealed primary hyperparathyroidism associated with a parathyroid adenoma and elevated serum and urine metanephrines and norepinephrines. A computed tomography of the abdomen revealed a large heterogeneous right adrenal mass measuring 7.9 cm × 6.8 cm × 8 cm consistent with a pheochromocytoma. The patient subsequently underwent adrenal mass resection and a complete thyroidectomy and parathyroidectomy. Early recognition and treatment of multiple endocrine neoplasia 2A can possibly reduce the risk of lethal heart disease in addition to the other associated endocrine disturbances.

Indexed as

coronary artery diseasehyperparathyroidMEN 2Apheochromocytoma

Identifiers

PMID38022857
PMCPMC10655645
OpenAlexW4388738441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.