Lin Lu, Chen Cunren, Fang Tuanyu, Chen Daoxiong, Chen Kaining, Quan Huibiao
Department of Endocrinology, Hainan General Hospital, No. 19, Xiuhua Road, Xiuying District, Haikou City, Hainan Province, China.
J Med Case Rep. 2019 Nov 27;13(1):347. doi: 10.1186/s13256-019-2304-4.
Type A insulin resistance syndrome, one type of the hereditary insulin resistance syndromes, is a rare disorder. Patients with type A insulin resistance syndrome are nonobese and demonstrate severe hyperinsulinemia, hyperandrogenism, and acanthosis nigricans. The clinical features are more severe in affected females than in males, and they mostly become apparent at the age of puberty. In many cases, when severe insulin resistance is covered up by other signs or symptoms of type A insulin resistance syndrome, patients are often easily misdiagnosed with other diseases, such as polycystic ovary syndrome.
Our patient was a 27-year-old Han Chinese woman who sought treatment because of a menstrual disorder and hirsutism. Tests showed that her levels of insulin and testosterone were elevated, and gynecological color Doppler ultrasound suggested multiple cystic changes in the bilateral ovaries. After a diagnosis of polycystic ovary syndrome was made, pulsatile gonadotropin-releasing hormone therapy and metformin were administered, but the patient's symptoms did not improve in 1 year of follow-up. Considering that the previous diagnosis might have been incorrect, venous blood samples were collected from the patient and her relatives for genetic analysis. Subsequently, using Illumina sequencing, it was found that the proband, her father, and two brothers all had the c.3601C>T heterozygous missense mutation in exon 20 of the insulin receptor gene. The diagnosis was corrected to type A insulin resistance syndrome, and the patient's treatment was modified.
We report a case of a young woman with type A insulin resistance syndrome that was misdiagnosed as polycystic ovary syndrome. We discuss the causes, clinical features, diagnosis, and treatment of type A insulin resistance syndrome to improve the recognition of the disease and reduce its misdiagnosis. Female patients with high androgen levels and severe hyperinsulinemia should be considered for the possibility of hereditary insulin resistance syndromes (such as type A insulin resistance syndrome). Gene sequencing helps in making an early diagnosis and developing a targeted treatment strategy.
A型胰岛素抵抗综合征是遗传性胰岛素抵抗综合征的一种,是一种罕见疾病。A型胰岛素抵抗综合征患者不肥胖,表现为严重的高胰岛素血症、高雄激素血症和黑棘皮症。受累女性的临床特征比男性更严重,且大多在青春期显现。在许多情况下,当严重的胰岛素抵抗被A型胰岛素抵抗综合征的其他体征或症状掩盖时,患者常易被误诊为其他疾病,如多囊卵巢综合征。
我们的患者是一名27岁的汉族女性,因月经紊乱和多毛症前来就诊。检查显示她的胰岛素和睾酮水平升高,妇科彩色多普勒超声提示双侧卵巢有多个囊性改变。在诊断为多囊卵巢综合征后,给予脉冲式促性腺激素释放激素治疗和二甲双胍,但患者在1年的随访中症状未改善。考虑到之前的诊断可能有误,采集了患者及其亲属的静脉血样本进行基因分析。随后,通过Illumina测序发现,先证者、她的父亲和两个兄弟在胰岛素受体基因外显子20均有c.3601C>T杂合错义突变。诊断被纠正为A型胰岛素抵抗综合征,患者的治疗方案也随之调整。
我们报告了一例年轻女性A型胰岛素抵抗综合征被误诊为多囊卵巢综合征的病例。我们讨论了A型胰岛素抵抗综合征的病因、临床特征、诊断和治疗,以提高对该疾病的认识并减少误诊。对于雄激素水平高和严重高胰岛素血症的女性患者,应考虑遗传性胰岛素抵抗综合征(如A型胰岛素抵抗综合征)的可能性。基因测序有助于早期诊断并制定针对性的治疗策略。