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成涎细胞瘤为一种发生于腮腺或颌下腺的具有潜在侵袭性的肿瘤,通常出生时即已存在,肿瘤重现了原始涎腺的始基结构。成涎细胞瘤非常罕见,其临床表现虽然具有一定的特点,但肿瘤在组织学形态方面与多种其他肿瘤有重叠,诊断往往较为困难,而且预后很难预测,因此,及时有效地做出正确的病理学诊断具有十分重要的临床意义。本文着重对成涎细胞瘤的临床病理学特点、病理诊断与鉴别诊断等作一探讨。
Operitoneal tumor is a potentially aggressive tumor that occurs in the parotid or submandibular glands and usually exists at birth. The tumor reproduces the primordial structure of the original salivary gland. Operitoneal tumor is very rare, although its clinical manifestations have certain characteristics, but the histological morphology of the tumor overlap with a variety of other tumors, the diagnosis is often more difficult, and the prognosis is difficult to predict, so timely and effective to make the right The pathological diagnosis has very important clinical significance. This article focuses on the clinicopathological features of salivary tumor, pathological diagnosis and differential diagnosis for a discussion.