Journal Basic Info

  • Impact Factor: 0.285**
  • H-Index: 6
  • ISSN: 2638-4558
  • DOI: 10.25107/2638-4558
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Orthopedics & Rheumatology
  •  Veterinary Sciences
  •  Nuclear Medicine
  •  Chemotherapy
  •  Internal Medicine
  •  Cardio-Thoracic Surgery
  •  Geriatric Medicine
  •  Women’s Health Care

Abstract

Citation: Clin Case Rep Int. 2020;4(1):1156.DOI: 10.25107/2638-4558.1156

Checkpoint Inhibitor Develops Histological Autoimmune Pancreatitis Like Type 1 Diabetes: a Case Report

Mazzucato M, Garelli S, Presotto F, Betterle C and De Riva C

Department of Endocrine and Metabolic Diseases, Mestre Hospital, Italy Department of Internal Medicine, Mestre Hospital, Italy Department of Endocrinology, Padua University, Italy

*Correspondance to: De Riva C 

 PDF  Full Text Rapid Communication | Open Access

Abstract:

Background: Immune checkpoint inhibitors are new cancer drugs that act stimulating immune adapted response of patient to obtain tumor regression. Immunotherapy can generate immunerelated adverse events involved all organs, in particular checkpoint inhibitors PD1/PDL1 can develop autoimmune type 1 diabetes. Case Presentation: A 64 years old man affected by metastatic non-small cell lung carcinoma, after conventional therapy, was treated with pembrolizumab (a PD1/PDL1 checkpoint inhibitor): After ten weeks, he showed hyperglycemia with ketosis, stable reduced c-peptide, and positive anti-glutamic acid decarboxylase antibodies therefore he was treated with insulin injection. The histological image of pancreas appeared like an immune-mediated insulitis. Conclusion: New guidelines are recently published to inform clinicians and patients about frequent immune adverse events of these new immunotherapies.

Keywords:

Cite the Article:

Mazzucato M, Garelli S, Presotto F, Betterle C, De Riva C. Checkpoint Inhibitor Develops Histological Autoimmune Pancreatitis Like Type 1 Diabetes: a Case Report. Clin Case Rep Int. 2020; 4: 1156.

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