Abstract
Cushing’s syndrome (CS) is an immunocompromised state characterized by impaired cellular and adaptive immunity due to hypercortisolism. This imbalance in the immune system leads to a high risk of opportunistic infections which can potentially prove fatal. In such patients, mortality can be reduced with early diagnosis and effective management of the underlying hypercortisolism. In this case report, we describe how prompt reduction of cortisol levels using a low dose continuous etomidate infusion was pivotal in effective treatment of an opportunistic infection, disseminated nocardiosis, in a 29-year-old female with Cushing’s syndrome. We also discuss how treatment with antibiotics including empiric therapy with Imipenem and sulfamethoxazole/trimethoprim (SMX/TMP) and definite therapy as per susceptibility testing, with amikacin, SMX/TMP, and doxycycline helped to prevent adverse outcomes. Through this case, we aim to emphasize that infiltrates or cavitary lesions on the computed tomography (CT) scan of the chest in a patient with Cushing’s syndrome should raise concern for nocardiosis, and prompt management with antibiotics should be initiated. Similarly, disseminated nocardiosis should always raise concern for possible immune deficiency states like Cushing’s syndrome. Our case is unique in detailing the significance of using etomidate to acutely lower cortisol levels in a patient with endogenous CS and widespread invasive opportunistic infection. The pharmacology aspects of the Etomidate, in this case, have been published in the Journal of Pharmacy Practice and cited appropriately in this article.
Highlights
IntroductionEndogenous Cushing's syndrome is associated with increased morbidity and mortality, and prompt diagnosis and treatment are essential in mitigating the detrimental effects of cortisol excess
Cushing's syndrome (CS) is a disease characterized by prolonged hypercortisolism
We describe how prompt reduction of cortisol levels using a low dose continuous etomidate infusion was pivotal in effective treatment of an opportunistic infection, disseminated nocardiosis, in a 29-year-old female with Cushing’s syndrome
Summary
Endogenous Cushing's syndrome is associated with increased morbidity and mortality, and prompt diagnosis and treatment are essential in mitigating the detrimental effects of cortisol excess. Infections occurring due to impaired cellular immunity from excess circulating cortisol are among the leading cause of death in CS [1]. In such cases, resolution of underlying hypercortisolism is pivotal in treating the infection. A previously healthy patient with invasive nocardiosis should be investigated for the presence of cellular immunodeficiency given this strong association. We present a case of a young woman who presented with life-threatening disseminated nocardiosis in the setting of severe endogenous hypercortisolism, where timely use of etomidate was pivotal in management
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