Subcutaneous calcifications and hypothyroidism: Is there a missing link?

D. Giri, Ravi Jayaram, S. Senniappan
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Abstract

A 5-year-old boy was referred with a history of multiple subcutaneous nodules since infancy. He was born at 42 weeks gestation with a birth weight of 3.2 kg. At 8 months of age, he was noted to have an excessive weight gain by the health visitor and was subsequently diagnosed with primary hypothyroidism and commenced on levothyroxine 50 μg once daily. He had a normal newborn congenital hypothyroidism screen. The thyroid autoimmune antibodies were normal. By the age of 5 years, he had delayed walking, speech and learning difficulties. Mother gave a history of surgically removed calcified lesions on her back. His weight and height at presentation were 35.5 kg (+3.8 SDS) and 121.4 cm (1.6 SDS), respectively. On examination, he had multiple subcutaneous nodules over and behind the left knee, left forearm, right ankle, chest and abdomen (figures 1 and 2). Investigations revealed a …
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皮下钙化和甲状腺功能减退:是否有缺失的环节?
一名5岁男童自婴儿期起就有多个皮下结节病史。他在怀孕42周时出生,出生体重为3.2公斤。8个月大时,卫生访视员注意到他体重过度增加,随后诊断为原发性甲状腺功能减退,并开始服用左旋甲状腺素50 μg,每日一次。他有一个正常的新生儿先天性甲状腺功能减退症筛查。甲状腺自身免疫抗体正常。5岁时,他出现了走路迟缓、语言和学习困难。母亲讲述了她背部手术切除钙化病灶的病史。发病时体重35.5 kg (+3.8 SDS),身高121.4 cm (1.6 SDS)。检查发现,患者左膝、左前臂、右脚踝、胸部和腹部有多发皮下结节(图1和2)。
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