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Functional Adrenal Collision Tumor in a Patient with Cushing's Syndrome
Cathy Zhou1, Ghaneh Fananapazir1, Michael J Campbell2
1Department of Radiology, University of California, Davis Medical Center, Sacramento, CA, USA.
Case Reports in Endocrinology
|January 8, 2021
Summary
Rare adrenal collision tumors present diagnostic challenges. A case highlights the need for functional workup of presumed myelolipomas, as they can be hormonally active tumors.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Adrenal collision tumors, a rare entity, pose diagnostic difficulties.
- Myelolipomas are benign adrenal tumors containing mature adipose tissue and hematopoietic elements.
- Cushing's syndrome is characterized by excessive cortisol production.
Observation:
- A 45-year-old woman with obesity and diabetes mellitus presented with an incidentally discovered adrenal mass.
- Initial imaging suggested a myelolipoma due to the presence of macroscopic fat.
- Functional workup revealed adrenocorticotropic hormone- (ACTH-) independent Cushing's syndrome.
Findings:
- The adrenal mass was pathologically confirmed as a collision tumor comprising an adrenocortical adenoma and a myelolipoma.
- Laparoscopic adrenalectomy was performed successfully.
- Postoperative improvement in clinical symptoms, body mass index, and hemoglobin A1C was observed.
Implications:
- Clinicians should consider functional evaluation for adrenal masses with features suggestive of myelolipoma.
- Hormonally active collision tumors can mimic benign conditions, necessitating thorough investigation.
- Early diagnosis and treatment of adrenal collision tumors can lead to significant clinical improvement.
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