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一名有肺结核病史患者同时出现淀粉样甲状腺肿和脂肪化生:病例报告

Co-occurrence of Amyloid Goiter and Adipose Metaplasia in a Patient With History of Pulmonary Tuberculosis: A Case Report.

作者信息

Ahmed Khan Zain, Ahmad Sadaf, Williams Rajkumar, Gnanasambandam Kumaragurubaran, Lakshminarayanan Mekala

机构信息

Department of General Surgery, Billroth Hospitals, Chennai, IND.

Department of Histopathology, Apollo Cancer Centre, Chennai, IND.

出版信息

Cureus. 2023 Mar 11;15(3):e36008. doi: 10.7759/cureus.36008. eCollection 2023 Mar.

Abstract

Amyloid goiter is described as an accumulation of amyloid, an amorphous proteinaceous material, in the thyroid gland. The deposition of amyloid is relatively common in the thyroid gland. However, a significant clinical enlargement due to amyloid accumulation and fat deposition in the thyroid stroma resulting in diffuse goiter leading to compressive symptoms is a rare phenomenon. In this report, we describe a rare case of amyloid goiter with adipose metaplasia in a 38-year-old woman with a history of pulmonary tuberculosis who presented to the outpatient department with complaints of heartburn, abdominal discomfort, and hoarseness of voice. Incidentally patient had diffused multinodular neck swelling. Preliminary blood investigations were normal. The contrast-enhanced computed tomography neck showed multiple non-enhancing lesions and a diffusely enlarged thyroid gland, causing a mass effect on the oropharynx posteriorly and minimally on the trachea. Fine needle aspiration cytology thyroid revealed thyroiditis. The patient underwent a total thyroidectomy, and histopathological examination of the specimen showed an extracellular eosinophilic amorphous substance that was positive for Congo red and showed apple-green birefringence under polarized light, and large areas of adipose metaplasia were noted, and a diagnosis was made. The amyloid involvement can result from localized primary deposition or secondary to chronic inflammatory disease. The prevalence of amyloid goiter in developed countries is due to primary amyloidosis, and in developing countries is due to secondary amyloidosis. Patients with a history of pulmonary tuberculosis commonly present with renal amyloidosis as its complication. Patients with an enlarged thyroid gland and a history of chronic inflammatory conditions or plasma cell dyscrasias should be evaluated with extreme suspicion. The correlation of tuberculosis with the subsequent development of amyloid goiter highlights the need for research in this area.

摘要

淀粉样变甲状腺肿被描述为淀粉样物质(一种无定形蛋白质物质)在甲状腺内的积聚。淀粉样物质在甲状腺中的沉积相对常见。然而,由于淀粉样物质积聚和甲状腺基质中的脂肪沉积导致显著的临床甲状腺肿大,进而形成弥漫性甲状腺肿并引起压迫症状,这是一种罕见的现象。在本报告中,我们描述了一例罕见的淀粉样变甲状腺肿合并脂肪化生病例,患者为一名38岁女性,有肺结核病史,因烧心、腹部不适和声音嘶哑就诊于门诊。偶然发现患者颈部有弥漫性多发结节性肿胀。初步血液检查正常。颈部增强计算机断层扫描显示多个无强化病灶以及甲状腺弥漫性肿大,对后方口咽造成占位效应,对气管的影响较小。甲状腺细针穿刺细胞学检查显示为甲状腺炎。患者接受了甲状腺全切除术,标本的组织病理学检查显示有一种细胞外嗜酸性无定形物质,刚果红染色阳性,在偏振光下呈苹果绿双折射,可见大片脂肪化生,据此做出诊断。淀粉样物质累及可由局部原发性沉积或继发于慢性炎症性疾病引起。发达国家淀粉样变甲状腺肿的患病率归因于原发性淀粉样变性,而发展中国家则归因于继发性淀粉样变性。有肺结核病史的患者通常会出现肾淀粉样变性作为其并发症。甲状腺肿大且有慢性炎症性疾病或浆细胞发育异常病史的患者应高度怀疑并进行评估。结核病与随后发生的淀粉样变甲状腺肿之间的关联凸显了该领域研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed5/10084481/f7ca2d06bb73/cureus-0015-00000036008-i01.jpg

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