Evidence map›Paper›PMID 36757535›Full record

ReviewClinical rheumatology2023

Myopathic syndrome revealing a rare condition: Sheehan syndrome, a case-based review.

Elena Gradinaru, Catalin Furculescu, Andreea Trandafir, Daniela Opris-Belinski, Ioana Cristina Saulescu

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Clinical rheumatology, 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
0.6field-weighted citation impact, top 31% 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, 3 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

5 authors at 2 institutions in 1 country.

Elena GradinaruDepartment of Internal Medicine and Rheumatology, Sfanta Maria" Hospital, 011172, Bucharest, Romania.ORCID http://orcid.org/0000-0001-6759-0672
Catalin FurculescuDepartment of Internal Medicine and Rheumatology, Sfanta Maria" Hospital, 011172, Bucharest, Romania.
Andreea TrandafirDepartment of Internal Medicine and Rheumatology, Sfanta Maria" Hospital, 011172, Bucharest, Romania.ORCID http://orcid.org/0000-0003-1369-3873
Daniela Opris-Belinski *Department of Internal Medicine and Rheumatology, Sfanta Maria" Hospital, 011172, Bucharest, Romania.ORCID http://orcid.org/0000-0003-3883-9672
Ioana Cristina Saulescu *Department of Internal Medicine and Rheumatology, Sfanta Maria" Hospital, 011172, Bucharest, Romania. ioana.saulescu@umfcd.ro.ORCID http://orcid.org/0000-0001-8086-7330
Carol Davila University of Medicine and Pharmacy · ROClinical Emergency Hospital Bucharest · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This report presents a case of a Sheehan syndrome diagnosed with a delay of 29 years after occurrence of first symptoms, following a laborious birth ended with dead fetus and massive hemorrhage. The 50-year-old patient, with early menopause from the age of 21, is referred to our rheumatology department to investigate the etiology of a myopathic syndrome, which started 2 months before and gradually worsened. The differential diagnosis took into consideration the autoimmune, infectious, paraneoplastic, endocrinological, and drug-induced myopathic syndrome. Paraclinical investigations revealed panhypopituitarism, and cerebral magnetic resonance imaging detected empty-sella. The etiology of a myopathic syndrome is often multifactorial; therefore, it is important to continue the investigations even after identifying one possible etiological factor, especially when it does not seem to fully explain the clinical-paraclinical picture. Usually, the multiple dimensions of panhypopituitarism bring the patient to various medical specialties depending on the dominant symptomatology. Given the rarity of the above-mentioned syndrome in the present, and the long gap between the initial event and the final diagnosis, its identification continues to be a challenge.

Indexed as

Empty Sella SyndromeHypopituitarismFemaleHumansInfantMiddle AgedEmpty-sellaMyopathic syndromePanhypopituitarismSheehan syndrome

Identifiers

PMID36757535
OpenAlexW4319656603

What OpenQuestion holds

Textmetadata
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.