Evidence map›Paper›PMID 39463632›Full record

ArticleCureus2024

Challenges in Diagnosing Addison's Disease: A Case Report.

Joana Nascimento, Frederico Silva, Tiago Vasconcelos, Inês G Simões, Raquel Pinho

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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
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.

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

5 authors.

Joana NascimentoInternal Medicine, Centro Hospitalar Universitário do Algarve, Unidade de Portimão, Portimão, PRT.
Frederico SilvaInternal Medicine, Centro Hospitalar Universitário do Algarve, Unidade de Portimão, Portimão, PRT.
Tiago VasconcelosInternal Medicine, Centro Hospitalar Universitário do Algarve, Unidade de Portimão, Portimão, PRT.
Inês G SimõesInternal Medicine, Centro Hospitalar Universitário do Algarve, Unidade de Portimão, Portimão, PRT.
Raquel PinhoInternal Medicine, Centro Hospitalar Universitário do Algarve, Unidade de Portimão, Portimão, PRT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Addison's disease, or primary adrenal insufficiency, is a rare condition characterized by a deficiency of adrenocortical hormones due to the damage of the adrenal glands. This case report presents a 36-year-old woman with a history of intestinal obstruction caused by adhesions and bands, who visited the emergency department with postprandial vomiting and epigastric discomfort. On physical examination, notable findings included bronzed skin, cutaneous hyperpigmentation, hyperpigmented scars and tongue, orange-colored teeth, decreased muscle strength in all four limbs, and mild gait imbalance. The patient also exhibited hyponatremia and hyperkalemia, which are common features of this disease. The diagnosis was confirmed by a computed tomography scan, which revealed adrenal gland calcifications. The patient was treated with hydrocortisone and fludrocortisone, resulting in significant clinical improvement. This case report underscores the importance of recognizing this condition and considering it in patients with nonspecific symptoms (fatigue, weight loss, and gastrointestinal disturbances), enabling effective therapy, including hormone replacement and continuous monitoring, which is crucial to optimize prognosis and prevent future complications.

Indexed as

acthaddison's diseasecutaneous hyperpigmentationhormone replacement therapyprimary adrenal insufficiency

Identifiers

PMID39463632
PMCPMC11506810

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.