From: Feminizing adrenocortical adenoma in a girl from a resource-limited setting: a case report
Date | Relevant past medical history and intervention |
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Before 2020 | The family noticed bilateral breast enlargement, sought medical advice in different primary care facilities and had been reassured |
Date | Summary | Testing | Interventions |
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First visit: 8 December 2020 | Patient presented at the age of 4 years and 5 months with gradually progressive bilateral breast enlargement since the age of 9 months, with accelerated growth | Left wrist X-ray: bone age of 8 years | Hormonal tests and abdominal ultrasound requested |
Second visit: 15 December 2020 | Investigations and imaging results | Basal luteinizing hormone 3.1 mIU/L prestimulation. Increased to 8.8 mIU/L 45 minutes post-gonadotrophin-releasing hormone stimulation Estradiol E2 29000 pg/mL (5–15 pg/mL) Dehydroepiandrosterone sulfate 90 ng/mL (2.3 ng/mL). Early morning cortisol level 16 ng/mL (7–28 ng/ml) Abdominal ultrasound showed a right-sided hypoechoic suprarenal mass | Abdominal CT scan requested. |
Third visit 22 December 2020 | Follow-up with abdominal CT scan result | Abdominal CT scan revealed a well-defined rounded focal lesion with a smooth outline at the level of the right adrenal gland with normal left adrenal gland and ovaries | Diagnosis of estrogen-secreting adrenocortical tumor and surgical referral |
Fourth visit 12 January 2021 | Postoperative evaluation, patient was clinically well | Normal cortisol and dehydroepiandrosterone sulfate. Estradiol E2 40 pg/mL consistent with central precocious puberty. | Patient started on gonadotrophin-releasing hormone agonist |
Fifth visit 15 June 2021 | Patient was well, compliant to monthly gonadotrophin agonist injections with partial regression of her secondary sexual characters and normal growth velocity (5 cm/year) | Abdominal CT scan was normal with no evidence of recurrence | To continue on gonadotrophin-releasing hormone agonist, with regular follow–up for the possibility of tumor recurrence |