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原发性甲状旁腺功能亢进症的非典型表现。

Atypical Presentation of Primary Hyperparathyroidism.

作者信息

Thu Win, Hashmi Aisha

机构信息

Diabetes and Endocrinology, University Hospitals Plymouth National Health Service (NHS) Trust, Plymouth, GBR.

出版信息

Cureus. 2024 Nov 24;16(11):e74337. doi: 10.7759/cureus.74337. eCollection 2024 Nov.

Abstract

Primary hyperparathyroidism (PHPT) typically presents with a spectrum of symptoms, including neuropsychiatric manifestations such as anxiety, depression, confusion, and, in severe cases, coma. While psychiatric symptoms are not uncommon in PHPT, acute psychosis is a rare presentation. In such cases, immediate control of serum calcium levels is crucial, and emergency parathyroidectomy may be required if medical management alone fails to control hypercalcemia. A middle-aged female was initially evaluated in the endocrine clinic for newly diagnosed asymptomatic PHPT and was scheduled for elective parathyroidectomy. However, she subsequently presented to the hospital with acute psychosis and elevated serum calcium levels. Despite aggressive intravenous fluid resuscitation and bisphosphonate therapy, her calcium levels and psychiatric symptoms did not improve. She underwent an emergency parathyroidectomy, during which three parathyroid adenomas were identified and removed. Postoperatively, her psychosis resolved, and her serum calcium levels normalized. Genetic testing later ruled out Multiple Endocrine Neoplasia (MEN) syndrome. Multiple parathyroid adenomas represent a rare but important subset of primary hyperparathyroidism. In cases with unusual presentations such as acute psychosis, prompt surgical intervention is essential, as it can lead to the rapid resolution of both hypercalcemia and neuropsychiatric symptoms. Genetic testing for MEN syndromes should be considered in cases of multiple adenomas to ensure appropriate follow-up and management.

摘要

原发性甲状旁腺功能亢进症(PHPT)通常表现出一系列症状,包括神经精神方面的表现,如焦虑、抑郁、意识模糊,严重时会出现昏迷。虽然精神症状在PHPT中并不罕见,但急性精神病是一种罕见的表现形式。在这种情况下,立即控制血清钙水平至关重要,如果仅靠药物治疗无法控制高钙血症,可能需要进行急诊甲状旁腺切除术。一名中年女性最初在内分泌门诊接受评估,被诊断为新发现的无症状PHPT,并计划进行择期甲状旁腺切除术。然而,她随后因急性精神病和血清钙水平升高入院。尽管进行了积极的静脉补液复苏和双膦酸盐治疗,她的钙水平和精神症状仍未改善。她接受了急诊甲状旁腺切除术,术中发现并切除了三个甲状旁腺腺瘤。术后,她的精神病症状消失,血清钙水平恢复正常。基因检测后来排除了多发性内分泌腺瘤病(MEN)综合征。多发性甲状旁腺腺瘤是原发性甲状旁腺功能亢进症中一个罕见但重要的亚组。在出现如急性精神病等不寻常表现的病例中,及时的手术干预至关重要,因为这可以迅速缓解高钙血症和神经精神症状。对于多发性腺瘤病例,应考虑进行MEN综合征的基因检测,以确保进行适当的随访和管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3992/11667644/fb0d54f4bdaf/cureus-0016-00000074337-i01.jpg

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