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与干燥综合征相关的颊黏膜局限性结节性淀粉样变:一例报告及文献复习

Localized Nodular Amyloidosis of the Buccal Mucosa Associated with Sjögren's Syndrome: A Case Report and Literature Review.

作者信息

Doi Rieko, Shimizu Kiharu, Fujii Nobuyuki, Sakai Kosuke, Kawasaki Makoto, Tamura Takayuki, Kodani Isamu

机构信息

Division of Oral and Maxillofacial Surgery, Department of Sensory and Motor Organs, School of Medicine, Faculty of Medicine, Tottori University, Yonago 683-8504, Japan.

Department of Oral Surgery, Yonago Medical Center, Yonago 683-0006, Japan.

出版信息

Yonago Acta Med. 2025 Jul 14;68(3):289-296. doi: 10.33160/yam.2025.08.009. eCollection 2025 Aug.

Abstract

Amyloidosis is a group of disorders in which specific precursor proteins form insoluble amyloid fibrils are deposited in various organs and extracellular spaces. Sjögren's syndrome (SS) is a chronic inflammatory disease in which lymphocytes infiltrate the exocrine glands, such as the salivary and lacrimal glands, through an autoimmune mechanism. At advanced stages of SS, localized nodular amyloidosis has been reported in specific organs outside the glands. Herein, we report a case of localized nodular amyloidosis associated with SS. An 80-year-old woman, who had been biting her buccal mucosa for several years and was aware of the presence of a mass, which had increased in size since approximately 6 months, was referred to our hospital. The patient had a history of SS and systemic lupus erythematosus since her 50s. A needle biopsy was performed because malignancy was suspected by magnetic resonance imaging. The pathological diagnosis was ATTR-type amyloidosis. The patient underwent excision of the lesion to improve the swelling. The pathological findings showed plasma cell infiltration in some areas, which required differentiation from AL amyloidosis; therefore, the patient was referred to a facility specializing in amyloidosis. The pathological diagnosis was AL amyloidosis. Various clinical findings ruled out systemic involvement and the final pathological diagnosis was localized nodular amyloidosis. It has been reported that it may occur in the advanced stages of SS, and our patient had SS for 30 years. One year after the surgery, the patient's prognosis was good.

摘要

淀粉样变性是一组疾病,其中特定的前体蛋白形成不溶性淀粉样原纤维并沉积在各种器官和细胞外间隙中。干燥综合征(SS)是一种慢性炎症性疾病,淋巴细胞通过自身免疫机制浸润外分泌腺,如唾液腺和泪腺。在SS的晚期,已报道在腺体以外的特定器官中出现局限性结节性淀粉样变性。在此,我们报告一例与SS相关的局限性结节性淀粉样变性病例。一名80岁女性,多年来一直咬颊黏膜,意识到有一个肿块,自大约6个月前以来肿块大小有所增加,被转诊至我院。该患者自50多岁起就有SS和系统性红斑狼疮病史。由于磁共振成像怀疑为恶性肿瘤,故进行了针吸活检。病理诊断为ATTR型淀粉样变性。患者接受了病变切除以改善肿胀。病理结果显示部分区域有浆细胞浸润,这需要与AL淀粉样变性相鉴别;因此,该患者被转诊至一家专门治疗淀粉样变性的机构。病理诊断为AL淀粉样变性。各种临床检查结果排除了全身受累,最终病理诊断为局限性结节性淀粉样变性。据报道,它可能发生在SS的晚期,而我们的患者患SS已有30年。手术后一年,患者预后良好。

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