TLDR A rare adrenal gland tumor can cause unusual symptoms due to hormone changes.
Adrenal myelolipoma was a rare benign tumor of the adrenal gland, typically asymptomatic and nonsecreting, often discovered incidentally. This case involved a 26-year-old female presenting with symptoms such as headache, acne, hoarseness, facial hair growth, poor breast development, and an enlarged clitoris. Elevated levels of serum testosterone, cortisol, androstenedione, and adrenocorticotropic hormone were noted. The patient underwent a left adrenalectomy, and histopathology revealed a tumor predominantly composed of adipose tissue with hemorrhage and hematopoietic elements. This case highlighted the unusual presentation of a large functional adrenal myelolipoma in a young adult female.
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May 2017 in “Human Reproduction Update” The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.
88 citations
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April 2017 in “Journal of Pediatric and Adolescent Gynecology” The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.
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April 2020 in “Clinical endocrinology and metabolism journal” Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.
11 citations
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January 2013 in “Indian Journal of Endocrinology and Metabolism” A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.
100 citations
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May 2011 in “Journal of Pediatric and Adolescent Gynecology” The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.
