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ArticleJCEM case reports2025

Myxedema Coma Nested Inside Sheehan Syndrome: A Diagnosis Not to Be Missed.

Pankaj Singhania, Abhranil Dhar, Ayush Agarwal, Ramamoorthy Ponnusamy, Priya Singhania

Abstract readCase Reports
In one paragraph

Article in JCEM case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Pankaj SinghaniaDepartment of Endocrinology and Obstetrics and Gynaecology, Arogyam Health Care, Purulia, West Bengal 723101, India.ORCID https://orcid.org/0000-0002-9392-3300
Abhranil DharDepartment of Endocrinology, IPGME&R, Kolkata, West Bengal 700020, India.
Ayush AgarwalDepartment of Endocrinology, IPGME&R, Kolkata, West Bengal 700020, India.
Ramamoorthy PonnusamyDepartment of Medicine, DMGMCH, Purulia, West Bengal 723147, India.
Priya SinghaniaDepartment of Endocrinology and Obstetrics and Gynaecology, Arogyam Health Care, Purulia, West Bengal 723101, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myxedema crisis is a life-threatening manifestation of severe, decompensated hypothyroidism. It often presents insidiously with altered mental status, hypothermia, hypotension, bradycardia, and hypoglycemia. Sheehan syndrome is a rare but important cause of hypopituitarism, resulting from ischemic necrosis of the anterior pituitary due to severe postpartum hemorrhage. The condition may remain undiagnosed for years, with subtle symptoms gradually progressing to full-blown endocrine crises during physiological stress. We report the case of a 48-year-old woman who presented with sudden unconsciousness, hypotension, bradycardia, hypoglycemia, and hyponatremia. Her obstetric history revealed massive postpartum hemorrhage 15 years back, followed by failure of lactation and secondary amenorrhea. Physical examination revealed madarosis. Laboratory investigations confirmed central hypothyroidism and secondary adrenal insufficiency. Magnetic resonance imaging (MRI) of brain showed an empty sella turcica, supporting the diagnosis of Sheehan syndrome. She was managed with intravenous hydrocortisone and replacement dose of levothyroxine. Considering the clinical deterioration after initial improvement, levothyroxine 500 μg loading dose was given, suspecting myxedema coma, which lead to gradual improvement of sensorium and hemodynamic status. This case highlights the importance of considering myxedema coma in women with Sheehan syndrome, especially in the setting of an unexplained altered sensorium even after hydrocortisone supplementation.

Indexed as

adrenal crisisempty sellahypopituitarismmyxedema comaSheehan syndrome

Identifiers

PMID40689303
PMCPMC12268321

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