Yang Mei, Zhang Zhaoqian, Zafar Sajid
Internal Medicine, St. Luke's Hospital, Chesterfield, USA.
Gastroenterology and Hepatology, St. Luke's Hospital, Chesterfield, USA.
Cureus. 2024 Jul 19;16(7):e64946. doi: 10.7759/cureus.64946. eCollection 2024 Jul.
Autoimmune pancreatitis (AIP) is acknowledged as a benign ailment with swift responsivity to corticosteroid treatment (CST). Though past assumptions dismissed its connection to cyst formation, a few instances of AIP-linked pancreatic cysts (PCs) have been documented. While some cases responded positively to CST, others demonstrated resistance, necessitating intervention. Our case is a 50-year-old male with a known diagnosis of type 1 AIP. This case presents a specific adverse drug reaction of glucocorticoid that causes diabetes mellitus. Glucocorticoid was tapered due to clinical improvement and diabetes complications but also caused multiple flares. Additionally, in several months, CT showed progressive enlarging multi-cystic pancreatic head lesions, which cause constriction at the distal duodenal outlet and biliary ductal dilation. This case presents a specific adverse drug reaction of glucocorticoid that causes diabetes mellitus. Meanwhile, the fast-growing multi-cysts in the pancreatic head after treatment of type 1 AIP were very rare.
自身免疫性胰腺炎(AIP)被认为是一种对皮质类固醇治疗(CST)反应迅速的良性疾病。尽管过去的假设否定了其与囊肿形成的关联,但已有一些AIP相关胰腺囊肿(PCs)的病例被记录。虽然一些病例对CST反应良好,但其他病例则表现出耐药性,需要进行干预。我们的病例是一名50岁男性,已知诊断为1型AIP。该病例呈现出糖皮质激素引起糖尿病的一种特殊药物不良反应。由于临床症状改善和糖尿病并发症,糖皮质激素逐渐减量,但也导致了多次病情复发。此外,在几个月内,CT显示胰腺头部多囊性病变逐渐增大,导致十二指肠远端出口狭窄和胆管扩张。该病例呈现出糖皮质激素引起糖尿病的一种特殊药物不良反应。同时,1型AIP治疗后胰腺头部快速生长的多囊非常罕见。