Lidang Jensen M, Kiaer H
Institute of Pathology, Skive and Svendborg Hospital, Aalborg, Denmark.
Pathol Res Pract. 1992 Feb;188(1-2):226-31; discussion 232-4. doi: 10.1016/S0344-0338(11)81187-8.
A rare case of a poorly-differentiated acinic cell carcinoma with primary presentation in a hyperplastic intraparotid lymph node, is reported. As the tumour mainly consisted of ductular and undifferentiated cells growing in solid cords, diagnosis was rendered difficult. Typical acinic cells were only rarely observed. In the multiple sections reviewed a single tumour nodulus occurred in salivary gland tissue outside the lymph node capsule. The possibility of a microscopic clinically occult primary acinic cell carcinoma that metastasized and presented primarily in an intraparotid lymph node, is mentioned. A multifocal origin in salivary tissue within and outside the intraglandular lymph node is another assumption, which is discussed. Differential diagnoses are mentioned and results of immuno- and histochemical studies are reported.
报告了1例原发性表现为腮腺内增生性淋巴结的低分化腺泡细胞癌罕见病例。由于肿瘤主要由呈实性条索状生长的导管样细胞和未分化细胞组成,诊断困难。仅偶尔观察到典型的腺泡细胞。在复查的多个切片中,在淋巴结包膜外的唾液腺组织中出现了单个肿瘤小结节。文中提到了一种微观上临床隐匿的原发性腺泡细胞癌转移并主要表现为腮腺内淋巴结的可能性。另一种假设是腺内淋巴结内外唾液组织的多灶性起源,并对此进行了讨论。文中提到了鉴别诊断并报告了免疫组化和组织化学研究结果。