涎腺异位囊肿复合体引起的多形性腺瘤:异位涎腺瘤的罕见来源。

IF 3.4 3区 医学 Q1 PATHOLOGY
Haley Corbin, Linwah Yip, Diana Bell, Raja R Seethala
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引用次数: 0

摘要

我们报告一例早期多形性腺瘤出现在涎腺异位(SH)与相关的k斯坦纳囊肿,所有在脂肪附近的高细胞甲状旁腺。sh -囊肿复合体与甲状旁腺的关联是一种反复出现的发现,可能起源于k斯坦纳管(KC),这是第三鳃裂囊中发育中的胸腺和下甲状旁腺的胚胎学残余。我们随后建立了KC的免疫表型(SOX-10阳性,甲状旁腺激素阴性,PAX-9变量),并证实SH-囊肿复合物的囊肿确实具有这种表型,并且正如预期的那样,与SH的腺泡和嵌入管成分共享SOX-10阳性。我们的病例显示与导管成分、浆细胞样肌上皮细胞和HMGA2反应性密切相关,证明了将其命名为早期多形性腺瘤是合理的。因此,这一偶然发现为没有已知原发灶的颈部原发性唾液腺肿瘤提供了另一种罕见但合理的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pleomorphic adenoma arising in salivary heterotopia-cyst complex of parathyroid: a rare origin for ectopic salivary gland neoplasia.

We report a case of an early pleomorphic adenoma arising in salivary heterotopia (SH) with an associated Kürsteiner cyst, all in the fat adjacent to a hypercellular parathyroid. The association of SH-cyst complexes with parathyroid is a recurring finding with suggested origin from Kürsteiner canals (KC), which are putative embryologic remnants of the developing thymus and inferior parathyroid glands in the third branchial pouches. We subsequently established the immunophenotype for KC (SOX-10 positive, parathyroid hormone negative, PAX-9 variable) and confirmed that the cysts of SH-cyst complexes do indeed have this phenotype and as expected, share SOX-10 positivity with the acinar and intercalated duct components of SH. Our case shows an intimate association with ductal elements, plasmacytoid myoepithelial cells, and HMGA2 reactivity, justifying designation as an incipient pleomorphic adenoma. Thus, this incidental finding provides another rare but plausible rationale for primary salivary gland tumors in the neck without a known primary.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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