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Occult ectopic adrenocorticotropic hormone secretion: diagnostic dilemma and infective consequence
Njideka Momah1, Thomas Koroscil1
1Wright State University, Dayton, OH, USA.
Clinics and Practice
|April 26, 2014
Summary
Ectopic adrenocorticotropic hormone (ACTH) secretion from a thymic neuroendocrine tumor caused Cushing's syndrome. Despite surgery and treatment, the patient succumbed to opportunistic infections, highlighting diagnostic challenges.
Area of Science:
- Endocrinology
- Oncology
- Infectious Diseases
Background:
- Ectopic adrenocorticotropic hormone (ACTH) secretion can cause Cushing's syndrome.
- Thymic neuroendocrine tumors are rare causes of ectopic ACTH production.
- Diagnosing occult ACTH-secreting tumors presents significant clinical challenges.
Observation:
- A 42-year-old male presented with symptoms of excess cortisol, including polyuria, polydipsia, and weight loss.
- Diagnostic workup revealed ectopic ACTH secretion, with imaging identifying an anterior mediastinal lesion.
- Fine needle aspiration confirmed a thymic neuroendocrine tumor.
Findings:
- Despite radical thymectomy, plasma ACTH and cortisol levels remained elevated, indicating persistent or unresectable disease.
- The patient developed disseminated intracranial aspergillosis, a fatal opportunistic infection.
- The case highlights the difficulty in diagnosing and managing ectopic ACTH-secreting thymic tumors.
Implications:
- Occult ectopic ACTH-secreting tumors pose a diagnostic dilemma requiring high clinical suspicion.
- Aggressive management and prompt treatment of opportunistic infections are crucial for patient survival.
- This case emphasizes the importance of considering rare endocrine and oncologic conditions in complex presentations.
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