Diagnosis and Treatment > Signs and Symptoms
Search for other papers by Stephanie Wei Ping Wong in
Google Scholar
PubMed
Search for other papers by Yew Wen Yap in
Google Scholar
PubMed
Search for other papers by Ram Prakash Narayanan in
Google Scholar
PubMed
Search for other papers by Mohammad Al-Jubouri in
Google Scholar
PubMed
Search for other papers by Ashley Grossman in
Google Scholar
PubMed
Search for other papers by Christina Daousi in
Google Scholar
PubMed
Search for other papers by Yahya Mahgoub in
Google Scholar
PubMed
Summary
We report our experience on managing a case of florid Cushing’s disease with Methicillin-resistant Staphylococcus aureus (MRSA) sepsis using intravenous etomidate in the intensive care unit of a UK district general hospital.
Learning points:
-
Severe Cushing’s syndrome is associated with high morbidity and mortality.
-
Etomidate is a safe and effective medical therapy to rapidly lower cortisol levels even in the context of severe sepsis and immunosuppression.
-
Etomidate should ideally be administered in an intensive care unit but is still feasible in a district general hospital.
-
During treatment with etomidate, accumulation of serum 11β-deoxycortisol (11DOC) levels can cross-react with laboratory cortisol measurement leading to falsely elevated serum cortisol levels. For this reason, serum cortisol measurement using a mass spectrometry assay should ideally be used to guide etomidate prescription.
Faculty of Medicine, Universiti Teknologi MARA, Sungai Buloh Campus, 47000 Sungai Buloh, Selangor, Malaysia
Search for other papers by S F Wan Muhammad Hatta in
Google Scholar
PubMed
Search for other papers by L Kandaswamy in
Google Scholar
PubMed
Search for other papers by C Gherman-Ciolac in
Google Scholar
PubMed
Search for other papers by J Mann in
Google Scholar
PubMed
Search for other papers by H N Buch in
Google Scholar
PubMed
Summary
Myopathy is a well-known complication of hypercortisolism and commonly involves proximal lower-limb girdle. We report a rare case of Cushing’s syndrome in a 60-year-old female presenting with significant respiratory muscle weakness and respiratory failure. She had history of rheumatoid arthritis, primary biliary cirrhosis and primary hypothyroidism and presented with weight gain and increasing shortness of breath. Investigations confirmed a restrictive defect with impaired gas transfer but with no significant parenchymatous pulmonary disease. Respiratory muscle test confirmed weakness of respiratory muscles and diaphragm. Biochemical and radiological investigations confirmed hypercortisolaemia secondary to a left adrenal tumour. Following adrenalectomy her respiratory symptoms improved along with an objective improvement in the respiratory muscle strength, diaphragmatic movement and pulmonary function test.
Learning points:
-
Cushing’s syndrome can present in many ways, a high index of suspicion is required for its diagnosis, as often patients present with only few of the pathognomonic symptoms and signs of the syndrome.
-
Proximal lower-limb girdle myopathy is common in Cushing’s syndrome. Less often long-term exposure of excess glucocorticoid production can also affect other muscles including respiratory muscle and the diaphragm leading to progressive shortness of breath and even acute respiratory failure.
-
Treatment of Cushing’s myopathy involves treating the underlying cause that is hypercortisolism. Various medications have been suggested to hinder the development of GC-induced myopathy, but their effects are poorly analysed.