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甲状腺脂肪瘤和甲状腺脂肪瘤病:5 例报告及文献复习。

Thyrolipoma and thyrolipomatosis: 5 case reports and historical review of the literature.

机构信息

Department of Pathology, Weill Medical College of Cornell University, The Methodist Hospital, Houston, TX 77030, USA.

出版信息

Ann Diagn Pathol. 2009 Dec;13(6):384-9. doi: 10.1016/j.anndiagpath.2009.08.003.

Abstract

Because thyrolipoma (adenolipoma of thyroid) and thyrolipomatosis (diffuse lipomatosis of thyroid) are distinctively rare conditions with only few cases reported in the literature, we are reporting 5 additional cases. All the 5 patients were adult females, with ages from 38 to 79 years, who presented with thyroid masses. Four of the patients had normal thyroid function tests and one had mild hypothyroidism. All patients received partial or total thyroidectomy. The thyroid specimens showed either circumscribed yellow-tan masses (cases 1, 2, and 3) or diffuse yellow-brown discoloration (cases 4 and 5). Histologic examination revealed abundant mature fat infiltrating the affected thyroid tissue in 3 distinct patterns: (1) fat infiltration limited to follicular adenomas (thyrolipoma); (2) fat diffusely infiltrating throughout the thyroid gland (thyrolipomatosis); or (3) fat infiltration involving both follicular adenoma and their surrounding thyroid tissue. Because of the rarity of thyroid fat-containing lesions, confusion in differential diagnosis may occasionally occur. It is important to be aware during frozen section that these lesions may present as extrathyroidal nodules, which can be radioactive on intraoperative scan for parathyroid glands. In addition, a papillary thyroid carcinoma was also identified in one case of thyrolipomatosis. All patients recovered well after surgery and there has been no recurrence of the lesions after 1 to 24 years of clinical follow-up. In summary, we are reporting 5 rare cases of thyrolipoma and thyrolipomatosis with distinct histologic patterns. Previously reported cases of thyrolipomatosis were reviewed and analyzed with the current cases.

摘要

由于甲状腺脂瘤(甲状腺腺瘤中的脂肪成分)和甲状腺脂肪增多症(甲状腺弥漫性脂肪增多症)是非常罕见的疾病,文献中仅报道了少数病例,我们报告了另外 5 例。这 5 例患者均为成年女性,年龄 38 至 79 岁,均表现为甲状腺肿块。4 例患者甲状腺功能检查正常,1 例有轻度甲状腺功能减退。所有患者均接受了部分或全部甲状腺切除术。甲状腺标本显示边界清楚的黄褐色肿块(病例 1、2 和 3)或弥漫性黄棕色变色(病例 4 和 5)。组织学检查显示,3 种不同模式下大量成熟脂肪浸润受累的甲状腺组织:(1)局限于滤泡性腺瘤的脂肪浸润(甲状腺脂瘤);(2)脂肪弥漫性浸润整个甲状腺(甲状腺脂肪增多症);或(3)滤泡性腺瘤及其周围甲状腺组织均有脂肪浸润。由于甲状腺含脂肪病变罕见,偶尔在鉴别诊断中可能会出现混淆。在冷冻切片中,重要的是要注意这些病变可能表现为甲状腺外结节,术中甲状旁腺扫描可能为放射性。此外,在一例甲状腺脂肪增多症中还发现了一例乳头状甲状腺癌。所有患者术后恢复良好,在 1 至 24 年的临床随访中病变无复发。总之,我们报告了 5 例罕见的甲状腺脂瘤和甲状腺脂肪增多症,具有明显的组织学模式。回顾并分析了以前报道的甲状腺脂肪增多症病例,并与目前的病例进行了分析。

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