Unexpected finding of thyroid hemiagenesis in a patient presenting with a right thyroid nodule and a history of Poland syndrome

C. Lame, B. Loum, P. Mazzaglia, C. Ndiaye, T. B. Diallo, A. Ndiaye, Ag Diouf, Aly Toure
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Abstract

Introduction: Poland syndrome is defined primarily by congenital absence of the pectoralis major. Thyroid hemiagenesis is the congenital absence of a single thyroid lobe. The combination of both pathologies has not been previously described. Case presentation: Poland syndrome is a rare congenital condition characterised by aplasia or hypoplasia of the pectoralis major muscle, associated to varying degrees with malformation of the ipsilateral upper limb. It is often accompanied by other congenital abnormalities, but the presence of a single thyroid lobe is exceptional. We report to our knowledge the first observation of thyroid hemiagenesis and Poland syndrome. Observation: A 19-year-old female was referred for chronic right neck swelling. On physical examination, she had a relatively small stature but an overall normal appearance. Neck examination revealed a mobile 3 cm right firm thyroid nodule. There was complete absence of the left breast and pectoralis muscles, with normal development on the right. The left hand was relatively small and exhibited syndactyly. Biochemical testing revealed normal thyroid function. Neck ultrasound revealed complete absence of the left thyroid lobe and the presence of a well-circumscribed hypoechoic 3 cm right thyroid nodule without calcifications, TIRADS score 3. The patient was diagnosed with Poland syndrome, a 3 cm right thyroid nodule, and agenesis of the left thyroid lobe. Her consent was obtained for a right thyroid lobectomy due to the cosmetic impact of the nodule, as well as the small risk that this represented a thyroid malignancy. An uncomplicated right thyroid lobectomy was performed. Final surgical pathology was consistent with a 3 cm benign follicular adenoma. Conclusion: Poland syndrome and thyroid hemiagenesis are both rare congenital malformations. Their association has not been previously described. Prior to surgery, the patient must be informed of the mandatory need for lifelong thyroid hormone replacement.
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出乎意料的发现甲状腺功能不全的病人表现为右甲状腺结节和波兰综合征的历史
波兰综合征的定义主要是先天性胸大肌缺失。甲状腺功能不全是先天性的单甲状腺叶缺失。这两种病理的结合以前没有被描述过。病例介绍:波兰综合征是一种罕见的先天性疾病,以胸大肌发育不全或发育不全为特征,不同程度伴有同侧上肢畸形。它通常伴有其他先天性异常,但单一甲状腺叶的存在是例外。据我们所知,我们报告了甲状腺功能不全和波兰综合征的首次观察。观察:一名19岁女性因慢性右颈部肿胀就诊。在体格检查中,她的身材相对较小,但整体外观正常。颈部检查发现一个移动的3厘米的右侧坚固甲状腺结节。左乳及胸肌完全缺失,右乳发育正常。左手相对较小,并指。生化检查显示甲状腺功能正常。颈部超声显示左侧甲状腺叶完全不见,右侧甲状腺结节边界清晰,低回声3厘米,无钙化,TIRADS评分3分。患者被诊断为波兰综合征,右侧甲状腺结节3厘米,左侧甲状腺叶发育不全。由于结节对美容的影响,以及这代表甲状腺恶性肿瘤的小风险,她同意进行右侧甲状腺小叶切除术。行无并发症的右侧甲状腺叶切除术。最终的手术病理是一个3厘米的良性滤泡腺瘤。结论:波兰综合征和甲状腺功能不全均为罕见的先天性畸形。他们之间的联系以前没有被描述过。手术前,必须告知患者必须终生更换甲状腺激素。
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