Suleman Sahar, Fatima Saira, Ud Din Nasir
Pathology and Laboratory Medicine/Histopathology, Aga Khan University Hospital, Karachi, PAK.
Histopathology, Aga Khan University, Karachi, PAK.
Cureus. 2024 Jun 25;16(6):e63134. doi: 10.7759/cureus.63134. eCollection 2024 Jun.
Acinic cell carcinoma (AciCC) is a rare clinical entity and a salivary gland malignancy. It is associated with wide histological variations in the cytomorphological patterns.
Sixty cases diagnosed as AciCC from 2002 to 2023 were assessed for diverse cytomorphological patterns.
The mean age of patients at the time of diagnosis was 44.35±16.8 years ranging from 15 to 81 years. Females comprised 58.3% for a F: M ratio of 1.4:1. Fifty three cases (88.3%) occurred in the parotid gland, two cases in the nasal region (3.3%), and one case each in the soft plate and upper lip (1.7%). The location of the remaining three cases was not specified. The most common presenting complaint was a well-defined facial swelling associated with pain. The average tumor size was 3.8±1.9 cm. The most predominant architectural pattern was solid (83.3%) followed by microcystic (60%), then follicular (41.7%), papillary cystic (14.3%), and tubulocystic (28.6%), and AciCC with de-differentiation/high-grade transformation was reported in three cases (5%). In 83.3% of the cases (50 out of 60), we noticed a mixture of two or more growth patterns. Other degenerative changes included prominent lymphoid stroma, hemorrhage, and cystic change.
Awareness and recognition of diverse cytomorphological patterns of AciCC, especially in institutions of a developing country where there is limited availability of highly specific and sensitive immunohistochemical stains or molecular diagnostics, are crucial and essential.
腺泡细胞癌(AciCC)是一种罕见的临床实体,属于涎腺恶性肿瘤。它与细胞形态学模式的广泛组织学变异相关。
对2002年至2023年诊断为AciCC的60例病例进行了多种细胞形态学模式评估。
诊断时患者的平均年龄为44.35±16.8岁,范围为15至81岁。女性占58.3%,男女比例为1.4:1。53例(88.3%)发生在腮腺,2例发生在鼻腔区域(3.3%),软腭和上唇各1例(1.7%)。其余3例的位置未明确说明。最常见的主诉是伴有疼痛的边界清晰的面部肿胀。平均肿瘤大小为3.8±1.9厘米。最主要的结构模式是实性(83.3%),其次是微囊状(60%),然后是滤泡状(41.7%)、乳头状囊状(14.3%)和管状囊状(28.6%),3例(5%)报告为伴有去分化/高级别转化的AciCC。在83.3%的病例(60例中的50例)中,我们注意到两种或更多生长模式的混合。其他退行性改变包括显著的淋巴间质、出血和囊性变。
认识和识别AciCC的多种细胞形态学模式至关重要,特别是在发展中国家的机构中,那里高特异性和敏感性的免疫组织化学染色或分子诊断的可用性有限。