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系统性轻链型淀粉样变性伴自主神经病变导致严重直立性低血压反复晕厥:一例报告

Systemic Amyloid Light Chain Amyloidosis With Repeated Syncope Due to Severe Orthostatic Hypotension Caused by Autonomic Neuropathy: A Case Report.

作者信息

Mori Yohei, Kenzaka Tsuneaki

机构信息

Department of General Medicine, Mitaki General Hospital, Yokkaichi, JPN.

Department of Internal Medicine, Hyogo Prefectural Tamba Medical Center, Tanba, JPN.

出版信息

Cureus. 2024 Nov 9;16(11):e73320. doi: 10.7759/cureus.73320. eCollection 2024 Nov.

Abstract

Amyloid light chain (AL) amyloidosis is a disease in which ALs, which are proteins with fibrous structures, are deposited in systemic organs, causing functional impairment. Diagnosis is often difficult because of non-specific and varied symptoms. We report a case of systemic AL amyloidosis that was diagnosed as a result of repeated syncope. A 76-year-old woman was brought to the emergency room with multiple episodes of loss of consciousness over the past five years. She visited the major hospital, where pulmonary thromboembolism and symptomatic epilepsy were considered possible causes. Orthostatic hypotension was observed after being transferred to our hospital for rehabilitation. We performed diagnostic tests, including blood tests, imaging, and a head-up tilt test, which confirmed severe orthostatic hypotension. A gastrointestinal biopsy with Congo red staining confirmed the presence of amyloid deposits. AL amyloidosis (λ) was diagnosed using immunohistochemical staining. Given her age and prolonged bed rest, she was determined that she could not tolerate chemotherapy and was discharged upon her request. To the best of our knowledge, this is the first report of systemic AL amyloidosis presenting with orthostatic hypotension severe enough to cause syncope due to autonomic neuropathy. Autonomic neuropathy should be considered, and amyloidosis should be included in the differential diagnosis when a patient presents with recurrent syncope.

摘要

淀粉样轻链(AL)淀粉样变性是一种疾病,其中具有纤维结构的蛋白质AL沉积在全身器官中,导致功能损害。由于症状不特异且多样,诊断往往很困难。我们报告一例因反复晕厥而被诊断为全身性AL淀粉样变性的病例。一名76岁女性因过去五年中多次意识丧失被送往急诊室。她曾就诊于一家大型医院,在那里肺血栓栓塞症和症状性癫痫被认为是可能的病因。转至我院进行康复治疗后,观察到体位性低血压。我们进行了包括血液检查、影像学检查和直立倾斜试验在内的诊断性检查,证实存在严重的体位性低血压。刚果红染色的胃肠道活检证实存在淀粉样沉积物。通过免疫组织化学染色诊断为AL淀粉样变性(λ型)。考虑到她的年龄和长期卧床休息情况,确定她无法耐受化疗,应其要求出院。据我们所知,这是首例因自主神经病变导致体位性低血压严重到足以引起晕厥的全身性AL淀粉样变性报告。当患者出现反复晕厥时,应考虑自主神经病变,并将淀粉样变性纳入鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c9a/11626683/81dd11cd94df/cureus-0016-00000073320-i01.jpg

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