The adverse effects of long-standing untreated hyperthyroidism on the bone were first described in 1891 by von Reckling Hausen in a 29-year-old woman who died after five years of hyperthyroidism. The changes described were predominantly those of bone destruction, with increased osteoclastic and osteoblastic activity, especially in cortical bones, causing high turnover osteoporosis and fractures. These changes have been described extensively in adults, but data in children are lacking. We report two cases of Graves' disease in children who had significant osteopenia and osteoporosis at diagnosis.
Case 1The patient was an 11-year-old Libyan girl who presented with low back pain after sustaining a fall on her back a day earlier. For the following two weeks, she complained of generalized weakness, shakiness of her hands and a protrusion of her left eye. There had also been a noticeable weight loss over the previous few months. Her past medical history was significant for congenital strabismus, for which she had repeated surgeries that had resulted in significant proptosis of the right eye. She had had speech delay since early childhood, which worsened with the recent tremors and weakness. On physical examination, she looked severely underweight (19 kg, below the 3rd centile), with a heart rate of 130/min., and blood pressure of 122/65 mm Hg. Her hands were warm, with obvious tremors bilaterally, and the eyes were proptotic, especially on the right side. She had significant kyphosis and tenderness on the thoracolumbar spine. A clinical diagnosis of Graves' disease was confirmed by biochemical findings of FT 4 of 69.1 pmol/L and TSH of less than 0.03 mU/L. Radiological examination of her spine revealed compression fracture of the T 6 and T 10 , as well as generalized severe osteopenia. Dual energy x-ray absorptiometry (DEXA) scan showed a significant loss of bone marrow density ( , and was encouraged to undertake active exercise. She showed significant clinical improvement in terms of her weakness and tremors. Compliance was a major problem. Her Ca, phosphorus and alkaline phosphatase were repeated once and were all normal. She was subsequently lost to follow-up for more than a year. A repeat DEXA scan was not done.
Case 2A 14-year-old boy presented with neck swelling, polyphagia, weight loss, increased sweating, nervousness and insomnia for a period of three weeks. He had previously been healthy and was not on any medications. His normal diet was rich in calcium (dairy products and vegetables), and he was active and athletic. Physical examination revealed an anxious, thinly built boy (37.7 kg, below the 3rd centile). He had exophthalmus, lid lag and retraction. The thyroid was diffusely enlarged with positive bruit. His hands were warm, sweaty and tremulous. His heart rate was 110/min., and blood pressure was 140/80. He was diagnosed with Graves' disease and was started on methimazole 30 mg daily, as well as propranolol. Thyroid function test showed a thyroxine level of 194 nmol/L, free thyroxine of 76.1 pmol/L and T...