Department of Tumor Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Pathol Int. 2010 Apr;60(4):326-9. doi: 10.1111/j.1440-1827.2010.02518.x.
A very rare case of necrotizing sialometaplasia of the parotid gland associated with angiocentric T-cell lymphoma was described. A 66-year-old male had left neck and pharyngeal masses and biopsy specimen showed a monotonous proliferation of atypical lymphoid cells with massive necrosis in the parotid gland. Angiocentric pattern or vascular invasion by the lymphoid cells was observed and the involved parotid gland exhibited squamous metaplasia of the ducts and acini; necrotizing sialometaplasia. Immunohistochemical analysis revealed a cytotoxic T-cell phenotype of the lymphoid cells (CD3+, CD4-, CD5+, CD8+, CD56-, Granzyme B+, TIA-1+, Perforin-) but in situ hybridization showed no relation to Epstein-Barr virus. Although necrotizing sialometaplasia is relatively rare in the parotid gland, angiocentric T-cell lymphoma should be considered for a causative condition of necrotizing sialometaplasia.
本文描述了一例罕见的腮腺血管中心性 T 细胞淋巴瘤伴坏死性涎腺化生。一名 66 岁男性出现左侧颈部和咽部肿块,活检标本显示腮腺内大量坏死的异型淋巴样细胞呈单形性增生。可见淋巴样细胞呈血管中心性或血管浸润性生长,受累腮腺导管和腺泡呈鳞状化生;坏死性涎腺化生。免疫组织化学分析显示淋巴样细胞具有细胞毒性 T 细胞表型(CD3+、CD4-、CD5+、CD8+、CD56-、Granzyme B+、TIA-1+、Perforin-),但原位杂交显示与 EBV 无关。尽管腮腺内坏死性涎腺化生相对罕见,但对于坏死性涎腺化生的病因,应考虑血管中心性 T 细胞淋巴瘤。