自身免疫性多腺体综合征 2 型一种罕见疾病的病例报告

Q4 Health Professions

Pakistan Armed Forces Medical Journal Pub Date : 2023-12-30 DOI:10.51253/pafmj.v73i6.8277

Wahaj Ul Hassan, U. Z. Farid, Kamran Ali, Umer Naseer

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摘要

自身免疫性多腺综合征（APS）是一种罕见的疾病，涉及多个内分泌和非内分泌器官。这些疾病通常很难诊断，因为其临床表现隐匿。我们介绍了一个病例，一名 29 岁的男子在感觉改变的状态下到急诊科就诊，并有局灶性癫痫发作病史。他的临床表现还包括低血压、乏力和复视。经过详细检查发现，他的多个内分泌腺受累，诊断为 APS。

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Autoimmune Polyglandular Syndrome Type-2 A Case Report on a Rare Disease

Autoimmune polyglandular syndromes (APS) are rare disorders involving multiple endocrine and non-endocrine organs. These are often difficult to diagnose, as the clinical presentation of these is insidious. We present a case where a 29-year-old man presented to the Emergency Department in a state of altered sensorium with a history of focal seizures. His clinical presentation further included hypotension, malaise, and diplopia. A detailed workup revealed multiple endocrine gland involvement, and a diagnosis of APS was made.

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