Hashmi Atif A, Iftikhar Syeda N, Haider Rimsha, Haider Raviha, Irfan Muhammad, Ali Javaria
Pathology, Liaquat National Hospital and Medical College, Karachi, PAK.
Internal Medicine, Liaquat National Hospital and Medical College, Karachi, PAK.
Cureus. 2020 Oct 26;12(10):e11172. doi: 10.7759/cureus.11172.
Introduction Solid papillary carcinoma (SPC) is a distinct rare subtype of breast tumour that often exhibits a neuroendocrine differentiation. Due to the rarity of these tumours, few studies have assessed the clinicopathological features of these tumours. Therefore, in this study, we evaluated the clinical and pathological profiles of SPC and compared the pathologic features with conventional invasive ductal carcinoma (IDC) in our population. Methods It was a retrospective cross-sectional study conducted at Liaquat National Hospital and Medical College from January 2013 until December 2019 over seven years. Cases with histological diagnosis of SPC and IDC were included in the study, and clinicopathological characteristics were compared. Results We included 39 cases of SPC in our study diagnosed during the study period. During the same timeline, 634 cases of IDC were reported and therefore included in the study for comparison. The mean age of the patients with SPC was 53.97 ± 12.15 years, and the mean tumour size was 3.42 ± 1.87 cm. Axillary metastasis was noted in 15.4% of cases. 94.9% of cases of SPC were invasive. Estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor-2 (HER2/neu) and synaptophysin positivity was seen in 84.6%, 87.2%, 10.3%, and 59% respectively. Recurrence was noted in 10.3% of cases with 94.9% survival rate. Cases of SPC had significantly lower grade (grade I + II), tumour (T) and nodal (N) stage than IDC. Moreover, the frequency of hormonal receptor expression (ER and PR) was higher, and the frequency of human epidermal growth factor receptor 2 (HER2/neu) expression was lower compared to IDC. Conclusion SPC is a distinct variant of malignant papillary breast tumours with overall better prognostic parameters than IDC. Therefore, it is essential to recognize the histological features of this rare breast tumour.
引言 实性乳头状癌(SPC)是一种独特的罕见乳腺肿瘤亚型,常表现出神经内分泌分化。由于这些肿瘤罕见,很少有研究评估其临床病理特征。因此,在本研究中,我们评估了实性乳头状癌的临床和病理特征,并将其病理特征与我们研究人群中的传统浸润性导管癌(IDC)进行了比较。
方法 这是一项回顾性横断面研究,于2013年1月至2019年12月在利亚卡特国家医院和医学院进行,为期七年。组织学诊断为实性乳头状癌和浸润性导管癌的病例纳入研究,并比较临床病理特征。
结果 我们的研究纳入了研究期间诊断的39例实性乳头状癌病例。在同一时间段内,报告了634例浸润性导管癌病例,因此也纳入研究进行比较。实性乳头状癌患者的平均年龄为53.97±12.15岁,平均肿瘤大小为3.42±1.87 cm。15.4%的病例出现腋窝转移。94.9%的实性乳头状癌病例为浸润性。雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(HER2/neu)和突触素阳性率分别为84.6%、87.2%、10.3%和59%。10.3%的病例出现复发,生存率为94.9%。实性乳头状癌病例的分级(I级+II级)、肿瘤(T)和淋巴结(N)分期明显低于浸润性导管癌。此外,与浸润性导管癌相比,激素受体表达(ER和PR)频率更高,人表皮生长因子受体2(HER2/neu)表达频率更低。
结论 实性乳头状癌是恶性乳头状乳腺肿瘤的一种独特变体,总体预后参数优于浸润性导管癌。因此,认识这种罕见乳腺肿瘤的组织学特征至关重要。