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首页> 外文期刊>Indian Journal of Pathology and Microbiology >Cytomorphological findings and histological correlation of papillary cystadenocarcinoma of the parotid: Not always a low-grade tumor
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Cytomorphological findings and histological correlation of papillary cystadenocarcinoma of the parotid: Not always a low-grade tumor

机译:腮腺乳头状囊腺癌的细胞形态学发现和组织学相关性:并非总是低度肿瘤

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摘要

Papillary cystadenocarcinoma (PCAC) is a rare salivary gland tumor characterized by a predominantly cystic growth that often exhibits intraluminal papillary growthwithout specific histologic features of other cystic salivary gland tumors. The preoperative cytological diagnosis can pose a diagnostic challenge as it has to bedifferentiated from other cystic papillary tumors such as mucoepidermoid carcinoma, papillary cystic variant of acinic cell carcinoma, and low-grade cribriform CAC. Itis considered to be a low-grade malignant salivary gland tumor with an indolent biological behavior. We report a case of PCAC of the parotid in a 55-year-old malediagnosed on fine needle aspiration cytology. Although it showed mild atypia cytologically, on excision tumor showed vascular and perineural invasion with regionalnode metastasis indicating a wider morphologic spectrum than what is described. This prompted us to write a case report describing the cytological and histologicalfeatures of this rare tumor and also discuss the diagnostic challenges.
机译:乳头状膀胱腺癌(PCAC)是一种罕见的唾液腺肿瘤,其特征在于主要为囊性生长,通常表现为管腔内乳头状生长,而没有其他囊性唾液腺肿瘤的特定组织学特征。术前细胞学诊断可能会带来诊断挑战,因为它必须与其他囊性乳头状瘤(例如粘液表皮样癌,腺泡状细胞癌的乳头状囊性变体和低度筛状CAC)区分开。它被认为是低度恶性唾液腺肿瘤,生物学行为低下。我们报告了55例经细针穿刺细胞学诊断为男性的腮腺PCAC病例。尽管在细胞学上显示出轻度的非典型性,但切除后的肿瘤表现为血管和神经周围的浸润,并伴有区域淋巴结转移,这表明其形态学谱比所描述的要宽。这促使我们撰写了一份病例报告,描述了这种罕见肿瘤的细胞学和组织学特征,并讨论了诊断挑战。

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