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黏液性水肿性精神病:神经精神症状及横纹肌溶解揭示甲状腺功能减退症

Myxedema Psychosis: Neuropsychiatric Manifestations and Rhabdomyolysis Unmasking Hypothyroidism.

作者信息

Sardar Sundus, Habib Mhd-Baraa, Sukik Aseel, Tanous Bashar, Mohamed Sara, Tahtouh Raad, Hamad Abdelrahman, Mohamed Mouhand F H

机构信息

Internal Medicine Residency Program, Internal Medicine Department, Hamad Medical Corporation, Doha, Qatar.

Internal Medicine Department, Hamad Medical Corporation, Doha, Qatar.

出版信息

Case Rep Psychiatry. 2020 Jun 22;2020:7801953. doi: 10.1155/2020/7801953. eCollection 2020.

Abstract

. Hypothyroidism is a prevalent endocrine disorder, often presenting with a spectrum of symptoms reflecting a hypothyroid state. It is also generally linked to causing mood swings, psychomotor slowing, and fatigue; however, in rare instances, it may lead to or induce acute psychosis, a condition referred to as myxedema psychosis (MP). We report a case of myxedema psychosis and present a literature review discussing its presentation, diagnosis, management, and prognosis. . A 36-year-old lady presented with one-week history of persecutory and paranoid delusions, along with visual and auditory hallucinations. She had no prior history of psychiatric illnesses. She underwent total thyroidectomy three years before the current presentation due to papillary thyroid cancer. She was not on regular follow-up, nor any specific therapy. On examination, she was agitated and violent. There were no signs of myxedema, and the physical exam was unremarkable. The initial workup showed a mild elevation in serum creatinine. Additional investigations revealed a high thyroid-stimulating hormone (TSH) of 56.6 mIU/L, low free T4 < 0.5 pmol/L, elevated creatine kinase of 3601 U/L, and urine dipstick positive for blood, suggestive of myoglobinuria. MRI of the head was unremarkable. We diagnosed her as a case of myxedema psychosis and mild rhabdomyolysis. She was started on oral thyroxine 100 mcg/day, fluoxetine 20 mg daily, and as-needed haloperidol. She was closely followed and later transferred to the Psychiatry Hospital for further management. Within one week, her symptoms improved completely, and she was discharged off antipsychotics with additional scheduled follow-ups to monitor TFTs and observe for any recurrence. . Myxedema psychosis is a rare presentation of hypothyroidism-a common endocrine disorder. Scarce data are describing this entity; hence, there is currently a lack of awareness amongst clinicians regarding proper identification and management. Moreover, the atypical nature of presentations occasionally adds to a diagnostic dilemma. Thus, any patient with new-onset psychosis should be screened for hypothyroidism, and awareness of this entity must be emphasized amongst clinicians and guideline makers.

摘要

甲状腺功能减退症是一种常见的内分泌疾病,常表现出一系列反映甲状腺功能减退状态的症状。它通常还与情绪波动、精神运动迟缓及疲劳有关;然而,在极少数情况下,它可能导致或诱发急性精神病,即黏液水肿性精神病(MP)。我们报告一例黏液水肿性精神病病例,并进行文献综述,讨论其临床表现、诊断、治疗及预后。一名36岁女性,有一周的被害妄想和偏执妄想病史,伴有视幻觉和听幻觉。她既往无精神疾病史。因乳头状甲状腺癌,她在本次就诊三年前接受了甲状腺全切术。她未进行定期随访,也未接受任何特殊治疗。检查时,她烦躁不安且有暴力倾向。无黏液水肿体征,体格检查无异常。初步检查显示血清肌酐轻度升高。进一步检查发现促甲状腺激素(TSH)高达56.6 mIU/L,游离T4低至<0.5 pmol/L,肌酸激酶升高至3601 U/L,尿试纸潜血阳性,提示肌红蛋白尿。头颅磁共振成像(MRI)无异常。我们诊断她为黏液水肿性精神病及轻度横纹肌溶解症。开始给予她口服左甲状腺素100 μg/天、氟西汀20 mg/天以及必要时使用的氟哌啶醇。对她进行密切随访,随后转至精神病医院进一步治疗。一周内,她的症状完全改善,停用抗精神病药物出院,并安排了额外的随访以监测甲状腺功能指标(TFTs)并观察是否复发。黏液水肿性精神病是甲状腺功能减退症(一种常见的内分泌疾病)的罕见表现。描述该病症的数据稀缺;因此,目前临床医生对其正确识别和治疗缺乏认识。此外,临床表现的非典型性有时会增加诊断难题。因此,任何新发精神病患者都应筛查甲状腺功能减退症,且必须向临床医生和指南制定者强调对该病症的认识。

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