Immunoglobulin G4-related Autoimmune Pancreatitis and Hypopituitarism Following Immune Checkpoint Inhibitor Therapy

被引:3
作者
Inoue, Saori [1 ]
Tsunoda, Yukiko [2 ]
Yamamoto, Kana
Okamoto, Hideki [1 ,3 ]
机构
[1] Meitetsu Hosp, Dept Endocrinol & Metab, Nagoya, Japan
[2] Meitetsu Hosp, Dept Urol, Nagoya, Japan
[3] Meitetsu Hosp, Dept Gastroenterol, Nagoya, Japan
关键词
immunoglobulin G4-related disease; autoimmune pancreatitis; hypopituitarism; immune checkpoint inhibitor; immune-related adverse events;
D O I
10.2169/internalmedicine.3591-24
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 70-year-old man underwent nephrectomy for renal cell carcinoma followed by 3 cycles of pembrolizumab as adjuvant chemotherapy. Three months later, he complained of appetite loss. He was diagnosed with secondary adrenal insufficiency and pancreatic tumor. Amylase and immunoglobulin G (IgG) 4 levels were normal. The differential diagnosis poses challenges in distinguishing pancreatic cancer, renal cell carcinoma metastasis, and autoimmune pancreatitis, necessitating tumor resection surgery. A histological examination revealed IgG4-related sclerosing pancreatitis. Postoperatively, there was no recurrence of pancreatitis. It is essential to consider the potential development of IgG4-related diseases after the administration of immune checkpoint inhibitors.
引用
收藏
页码:209 / 215
页数:7
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