ArticleBMJ case reports2019
A case of severe rhabdomyolysis associated with secondary adrenal insufficiency and autoimmune hepatitis.
Article in BMJ case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 7 citations in OpenAlex.
- Anterior hypopituitarism due to primary empty sella syndrome in a critically unwell patient.BMJ case reports · 2023Article
- Sheehan syndrome presenting as acute renal failure: A rare case report from Somalia.Annals of medicine and surgery (2012) · 2022Article
- A suspected case of hyponatraemia induced rhabdomyolysis: a case report.BMC nephrology · 2022Article
- From quail to earthquakes and human conflict: a historical perspective of rhabdomyolysis.Clinical kidney journal · 2021Review
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Rhabdomyolysis is a serious and life-threatening condition which has many established causes including endocrine disturbances. Of those, thyroid, adrenal and pituitary deficiencies are the most commonly seen. Most cases of rhabdomyolysis with adrenal insufficiency that have been reported have been primary. Here, we report an encounter with a patient who presented with her second case of severe rhabdomyolysis in the setting of secondary adrenal insufficiency. The cause for corticotropic suppression was most likely autoimmune hypophysitis given the presence of other autoimmune comorbidities including a new diagnosis of autoimmune hepatitis. In addition to her case, we present a brief review of the literature pertaining to cases of rhabdomyolysis attributed to adrenal insufficiency.
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