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Detailed case of a 6-year-old girl with progressive weight gain, excess hair growth, and a right hypochondrium mass suspected to be an adrenal tumor. Diagnosis, investigations, treatment, and postoperative care are discussed.
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CASE PRESENTATION BY AMANY IBRAHIM Assistant lecturer of Pediatrics CAIRO UNIVERSITY
Female patient 6yrs old with a history of progressive weight gain and increasing hair growth of 3 months duration. • On examination • She looks depressed. • She had moon plethoric face. • Buffalo hump, striae rubra. • Hirsuite, pubic hairs ( P4), acne, mild cliteromegaly. • Her height was 123.5 (on 97th centile = +2 SDS). • Weight was 29.5 kg (above 97th centile = +3 SDS). • BMI 19.3 (97th centile). • BP: 140/70 on different occasions. • Large firm mass in the right hypochondrium.
Based on the above data, the mass detected could be : • Pheochromocytoma. • Hepatocellular carcinoma. • Adrenal tumor.
Investigations • Free urinary cortisol 287ug /24hr(N 20-80) • S.cortisol ACTH Free urinary (ug/dl) (pg /ml) (ug/ml) am50 (N 6-16) 3.7 (N<82) 280 (N 20-80) pm 37 (N 3-11) 2.0 (N<82) LDDS 36 3 HDDS 37 2.2 180 DHEAS456u/dl (N 5-55u/dl). Testosterone7.2 ng/dl (N <0.5ng/dl). Na, K & PRA are normal.
Based on the above data, this patient suffers from: • Ectopic ACTH syndrome. • Cushing’s disease. • Adrenal tumor.
ADRENAL TUMORS • Two main characteristics of adrenal tumors: • They are autonomously secreting hormones. • They are unresponsive to manipulation of the hypothalamic pituitary adrenal axis with pharmacological agents. • Two main types of adrenal tumors: • Adenomas: present alone with manifestations of glucocorticoid excess (Cushing syndrome) with no manifestations of androgen excess. • Carcinomas: secrete multiple adrenocortical steroids (cortisol and androgen) even androgens in excess.
Suggested treatment modality for this case: • Surgical excision only. • Chemotherapy only. • Radiotherapy only. • Combined surgery, chemotherapy and radiotherapy.
PREOPERATIVELY • The patient received propranolol to control her blood pressure. • She had done an MRI abdomen, chest and bone scan to exclude metastasis. All were normal, apart from adrenal mass.
TREATMENT Unilateral right adrenalectomy (adrenal carcinoma) followed by chemotherapy.
POSTOPERATIVELY • She received steroid immediately after the operation and for 2 months, then withdrawn successfully. • She received mitotane followed by radiotherapy for with no recurrence. • She is now 10 years old and she is performing a yearly follow up of an MRI abdomen and chest, and serum DHEA-s, testosterone, cortisol which are so far normal.