Evidence map›Paper›PMID 41776570›Full record

ReviewJournal of medical case reports2026

Pitfalls in the management of undiagnosed secondary adrenal insufficiency: a case report and review of the literature.

Koharu Sakai, Tomohiko Yoshida, Takuyo Chiba, Masaya Yamaga, Minoru Takemoto

Abstract readCase ReportsReview
In one paragraph

Review in Journal of medical case reports, 2026. 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.

Koharu SakaiDepartment of Diabetes, Metabolism, and Endocrinology, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita-Shi, Chiba, 286-0124, Japan.
Tomohiko YoshidaDepartment of Diabetes, Metabolism, and Endocrinology, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita-Shi, Chiba, 286-0124, Japan. tomoyoshida@ihwg.jp.ORCID http://orcid.org/0000-0001-8887-7867
Takuyo ChibaDepartment of Emergency Medicine, International University of Health and Welfare, Narita Hospital, Chiba, 287-0124, Japan.
Masaya YamagaDepartment of Diabetes, Metabolism, and Endocrinology, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita-Shi, Chiba, 286-0124, Japan.
Minoru TakemotoDepartment of Diabetes, Metabolism, and Endocrinology, International University of Health and Welfare, Narita Hospital, 852 Hatakeda, Narita-Shi, Chiba, 286-0124, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProlonged cortisol deficiency in undiagnosed central adrenal insufficiency can lead to severe hypotonic hyponatremia due to inappropriate vasopressin secretion and malnutrition caused by inhibition of orexigenic signals. Notably, although hydrocortisone-induced recovery can trigger osmotic demyelination and refeeding syndromes, no previous report has simultaneously described these complications and documented significant decreases in vasopressin levels, along with changes in urine osmolality and volume before and after hydrocortisone administration. CASE PRESENTATION: A 48-year-old Japanese man presented with fever, severe nausea, and oliguria and was brought to our hospital by ambulance due to impaired consciousness. Physical examination and laboratory analysis showed severe euvolemic hypotonic hyponatremia and low-normal glucose value. Low adrenocorticotrophic hormone and cortisol levels, undetectable 24-hour urinary free cortisol, and minimal response to corticotropin-releasing hormone indicated secondary adrenal insufficiency. Magnetic resonance imaging revealed slight pituitary swelling, suggesting hypophysitis. Treatment started with a 200 mg hydrocortisone infusion over 24 hours, and 6 hours later, the patient experienced a marked decrease in vasopressin levels, accompanied by significant dilute urine excretion and an excessively rapid increase in blood sodium levels, which posed a risk of osmotic demyelination. Rehydration with 5% dextrose and desmopressin was used to prevent this risk. Carefully adjusting plasma osmolality successfully prevented osmotic demyelination syndrome. Hydrocortisone replacement significantly increased the patient's appetite, leading to refeeding hypophosphatemia and disorientation; however, these resolved with intravenous sodium phosphate replacement. The patient developed a fever on day 12 and was confirmed to have coronavirus disease 2019. The fever subsided by day 16 with molnupiravir treatment and hydrocortisone dose adjustment, and he was discharged on day 23 with a maintenance dose of hydrocortisone.

conclusionCareful management is required while administering hydrocortisone in patients with undiagnosed adrenal insufficiency, as it may cause osmotic demyelination syndrome or refeeding syndrome due to sudden changes in blood electrolytes.

Indexed as

Adrenal InsufficiencyHydrocortisoneHyponatremiaHypophysitisAdrenocorticotropic HormoneDemyelinating DiseasesFluid TherapyHumansMagnetic Resonance ImagingMaleMiddle AgedPituitary GlandRefeeding SyndromeTreatment OutcomeAdrenocorticotropic HormoneHydrocortisoneCase reportHyponatremiaOsmotic demyelination syndromeRefeeding syndromeUndiagnosed adrenal insufficiency

Identifiers

PMID41776570
PMCPMC13064267

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Registered trials

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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.