Cai Guoping, Bernstein Jane, Aslanian Harry R, Hui Pei, Chhieng David
Department of Pathology, Yale University School of Medicine, New Haven, Connecticut.
Department of Pathology, Yale University School of Medicine, New Haven, Connecticut.
J Am Soc Cytopathol. 2015 Jul-Aug;4(4):211-217. doi: 10.1016/j.jasc.2015.01.006. Epub 2015 Jan 21.
Autoimmune pancreatitis (AIP) is an inflammatory process that has characteristic clinical, radiographic, and pathologic features but may mimic pancreatic malignancy. In this study, we reviewed our experience in the endoscopic ultrasound-guided fine-needle aspiration evaluation of pancreatic lesions in patients with AIP.
We searched the cytopathology archives and identified a total of 6 cases that had endoscopic ultrasound-guided fine-needle aspiration evaluation and subsequent tissue biopsy or resection with a diagnosis of AIP. The clinical, cytologic, and histopathologic features were reviewed.
The original cytologic diagnoses included negative, atypical, and suspicious for malignancy in 2 cases each. On retrospective review, these cases were characterized cytologically by the presence of mixed epithelial cells, mixed lymphocytes, and plasma cells, as well as cellular stromal fragments. Cytologic atypia of epithelial cells was observed in 4 of 6 cases, including mild (3 cases) and moderate (1 case) atypia. KRAS mutation analysis was performed in 4 cases with an indeterminate cytology diagnosis, which was negative in all cases.
Our results demonstrate that the presence of trilineage epithelial, lymphoplasmacytic, and stromal elements may be suggestive but not definitive for a diagnosis of AIP. The role of KRAS mutation analysis in AIP remains inconclusive and may warrant further evaluation.
自身免疫性胰腺炎(AIP)是一种具有特征性临床、影像学和病理学特征的炎症过程,但可能酷似胰腺恶性肿瘤。在本研究中,我们回顾了我们对AIP患者胰腺病变进行内镜超声引导下细针穿刺活检评估的经验。
我们检索了细胞病理学档案,共识别出6例接受内镜超声引导下细针穿刺活检评估,随后进行组织活检或切除并诊断为AIP的病例。回顾了其临床、细胞学和组织病理学特征。
最初的细胞学诊断中,2例为阴性,2例为非典型性,2例为恶性可疑。回顾性分析显示,这些病例在细胞学上的特征为存在混合上皮细胞、混合淋巴细胞和浆细胞以及细胞性间质碎片。6例中有4例观察到上皮细胞的细胞学非典型性,包括轻度(3例)和中度(1例)非典型性。对4例细胞学诊断不明确的病例进行了KRAS突变分析,所有病例均为阴性。
我们的结果表明,三系上皮、淋巴浆细胞和间质成分的存在可能提示AIP诊断,但不具有决定性。KRAS突变分析在AIP中的作用仍不明确,可能需要进一步评估。