Abstract | OBJECTIVE: METHODS: We describe the initial manifestations, clinical investigations, and postoperative follow-up of the patient and review similar cases in the literature. RESULTS: A 5 and 9/12-year-old girl who was initially diagnosed and treated as having CAH and was noncompliant with glucocorticoid therapy presented with weight gain, hypertension, and a mass in the lower abdomen. On physical examination, she was a cushingoid-appearing girl with proximal muscle weakness and notable facial acne. Laboratory findings included elevated serum testosterone, 17-hydroxyprogesterone, dehydroepiandrosterone sulfate, androstenedione, estradiol, and cortisol, as well as elevated urinary cortisol and cortisone. Serum corticotropin was undetectable. She had normal serum electrolytes and plasma renin activity. Computed tomography scan of the abdomen and pelvis showed a cystic mass with a focal enhancing solid component arising from the right ovary, which was subsequently determined to be a steroid cell tumor not otherwise specified. CONCLUSION:
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Authors | Punkaj Gupta, Sunali Goyal, Luis E Gonzalez-Mendoza, Natan Noviski, Marko Vezmar, Carole D Brathwaite, Madhusmita Misra |
Journal | Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
(Endocr Pract)
Vol. 14
Issue 7
Pg. 875-9
(Oct 2008)
ISSN: 1934-2403 [Electronic] United States |
PMID | 18996816
(Publication Type: Case Reports, Journal Article, Review)
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Chemical References |
- Adrenocorticotropic Hormone
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Topics |
- Adrenal Hyperplasia, Congenital
(diagnosis, metabolism, pathology)
- Adrenocorticotropic Hormone
(metabolism)
- Child, Preschool
- Cushing Syndrome
(diagnosis, etiology, metabolism, pathology)
- Diagnostic Errors
- Female
- Humans
- Ovarian Neoplasms
(complications, metabolism, pathology)
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