具有管状上皮结构、实体上皮巢和间质成釉细胞相关蛋白沉积的罕见上颌肿瘤。伴淀粉样蛋白的中枢性牙源性纤维瘤的管状/针状变异?

IF 4.1
Head and neck pathology Pub Date : 2022-06-01 Epub Date: 2021-08-02 DOI:10.1007/s12105-021-01369-7
Ioannis G Koutlas, Katia Julissa Ponce, Rima-Marie Wazen, Antonio Nanci
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引用次数: 3

摘要

颌骨腺瘤最常表现为唾液腺的组织病理学特征,很少表现为皮肤腺瘤。它们被认为起源于牙源性上皮。一个不寻常的上颌肿瘤表现为放射在根尖周围区域的右永久侧切牙是一个74岁的男性提出引起牙根吸收。制备过程中偶有分支的管索和导管结构,其特征主要是由管腔立方到低柱状细胞角蛋白(CK) 7、berr - ep4和偶有CK8/18阳性细胞组成的双层结构,以及管腔、CK5/6阳性的基底/基底样细胞显示p63/p40的核反应性。平滑肌肌动蛋白和钙钙蛋白呈阴性,只有一小部分钙钙蛋白阳性细胞,证实缺乏肌上皮支持或上皮间质转化。CK19两层均有染色,管腔染色更强烈。嗜酸性分泌物质和偶尔的管腔膜被CK8/18和多克隆癌胚抗原(CEA)修饰。CD1a仅鉴定出罕见的朗格汉斯细胞,Ki67修饰了1-2%的输卵管细胞核。小而实的上皮细胞巢也可见。很少,一个明显的过渡到一个管状结构的巢被赞赏。部分炎症的间质表现为与淀粉样蛋白一致的多处透明化脱细胞沉积,其反应性为亮橙色刚果红,呈苹果绿双折射,与牙源性成釉细胞相关(ODAM)蛋白抗体反应,但与amelotin抗体和分泌性钙结合磷蛋白脯氨酸-谷氨酰胺抗体不反应1。综上所述,具有ODAM淀粉样蛋白的中枢性牙源性纤维瘤的管状/针状变异体的诊断是有利的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Unusual Maxillary Tumor with Tubuloductal Epithelial Structures, Solid Epithelial Nests and Stromal Odontogenic Ameloblast-Associated Protein Deposits. Tubuloductal/Syringoid Variant of Central Odontogenic Fibroma with Amyloid?

An Unusual Maxillary Tumor with Tubuloductal Epithelial Structures, Solid Epithelial Nests and Stromal Odontogenic Ameloblast-Associated Protein Deposits. Tubuloductal/Syringoid Variant of Central Odontogenic Fibroma with Amyloid?

Glandular tumors of jaw bones present, most often, histopathologic features of salivary gland and, rarely, of cutaneous glandular neoplasms. They are thought to originate from odontogenic epithelium. An unusual maxillary tumor presenting as a radiolucency in the periapical area of the right permanent lateral incisor of a 74-year-old male is presented causing root resorption. Preparations revealed occasionally branching tubular cords and ductal structures characterized, mostly, by a bilayer composed of luminal cuboidal to low columnar cytokeratin (CK) 7, Ber-EP4 and occasionally CK8/18 positive cells, and abluminal, CK5/6 positive, basal/basaloid cells revealing nuclear reactivity for p63/p40. Smooth muscle actin and calponin were negative, save for a single focus of calponin positive cells, confirming absence of myoepithelial support or epithelial mesenchymal transition. CK19 exhibited staining of both layers, the luminal being more intense. Eosinophilic secretory material and, occasionally, a luminal pellicle were decorated with CK8/18 and polyclonal carcinoembryonic antigen (CEA). CD1a identified only rare Langerhans' cells and Ki67 decorated 1-2% of abluminal cell nuclei. Small solid nests of epithelial cells were also present. Infrequently, an apparent transition of a nest into a tubular structure was appreciated. The partially inflamed stroma featured multiple hyalinized acellular deposits consistent with amyloid, as confirmed by bright orange Congo red reactivity with apple-green birefringence, which reacted with odontogenic ameloblast-associated (ODAM) protein antibody but not with antibodies for amelotin and secretory calcium-binding phosphoprotein proline-glutamine rich 1. Based on the above, the diagnosis of tubuloductal/syringoid variant of central odontogenic fibroma with ODAM amyloid is favored.

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