Cazacu I M, Chavez A A L, Saftoiu A, Whitlow T G, Bhosale P, Bhutani M S
Department of Gastroenterology, Hepatology, and Nutrition, University of Texas-MD Anderson Cancer Center, Houston, Texas, USA.
Department of Gastroenterology, Research Center of Gastroenterology and Hepatology, University of Medicine and Pharmacy Craiova, Romania.
Curr Health Sci J. 2018 Apr-Jun;44(2):181-185. doi: 10.12865/CHSJ.44.02.15. Epub 2018 Mar 27.
We report a rare case of seronegative autoimmune pancreatitis (AIP) that presented as a pancreatic focal lesion and was considered to be pancreatic cancer based on the clinical presentation and imaging findings. The endoscopic ultrasound-guided biopsies of the pancreatic mass revealed no malignant cells and the pancreatic swelling had become diffuse on repeat imaging. AIP was suspected and a trial of steroids was considered as a diagnostic and therapeutic method. The patient responded dramatically to corticosteroid treatment with resolution of symptoms and normal imagining and laboratory parameters. This case highlights the challenge in the diagnostic approach of a pancreatic mass.
我们报告了一例罕见的血清阴性自身免疫性胰腺炎(AIP),其表现为胰腺局灶性病变,基于临床表现和影像学检查结果曾被认为是胰腺癌。胰腺肿块的内镜超声引导下活检未发现恶性细胞,复查影像学检查时胰腺肿胀已变为弥漫性。怀疑为AIP,并考虑使用类固醇进行诊断性和治疗性试验。患者对皮质类固醇治疗反应显著,症状缓解,影像学和实验室参数恢复正常。该病例凸显了胰腺肿块诊断方法中的挑战。