Year: 2025
Type: article
Study design: Case Report
Abstract: Necrolytic migratory erythema(NME) is a rare dermatitis usually associated with pancreatic neuroendocrine tumor as a manifestation of glucogonoma syndrome. Over the past five years, NME has been scarcely reported in the literature, with only 8 cases globally. The age range of affected individuals spans from 28 to 62 years, with a mean onset age of 49.4 years. This report presents a 41-year-old male diagnosed with NME secondary to glucagonoma, highlighting the critical need for heightened clinical vigilance in younger NME patients. And NME can mimic other dermatological conditions, leading to potential misdiagnosis and late tumor identification. This case highlights the typical clinical features, aiming to enhance the diagnostic efficiency and accuracy for NME.
DOI: 10.2147/ccid.s508305
Authors: Di Xia, Zhouliang Liu, Jiamin Li, Jingjing Liu, Yongbin Qu
Institution: Southern Medical University
Language: English
Topic: Skin Diseases and Diabetes
Subfield: Dermatology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,836
OpenAlex ID: W4411965015
