Department of Pediatric Medicine, Lady Hardinge Medical College, Kalawati Saran Children's Hospital, New Delhi, India.
Indian J Pediatr. 2010 Jun;77(6):693-4. doi: 10.1007/s12098-010-0081-6. Epub 2010 Jun 8.
A 15-yr-old girl presented with bilateral gross ovarian tumors, clinical features of long-standing unrecognized hypothyroidism and markedly elevated CA-125 levels. Ovarian resection was avoided, as the presentation was consistent with the Van Wyk and Grumbach syndrome; and the patient was treated with replacement of thyroid hormone. Regression of the ovarian tumors occurred 6 months after initiation of the treatment. The authors emphasise the need for increased awareness and screening for hypothyroidism in patients with ovarian tumors, in order to prevent inadvertent operative interventions.
一位 15 岁女孩双侧卵巢出现巨大肿瘤,伴有长期未被识别的甲状腺功能减退的临床特征和明显升高的 CA-125 水平。由于表现符合范维克-格鲁姆巴赫综合征,避免了卵巢切除术,且对患者进行了甲状腺激素替代治疗。治疗开始后 6 个月,卵巢肿瘤开始消退。作者强调需要提高对卵巢肿瘤患者甲状腺功能减退症的认识和筛查,以防止意外的手术干预。