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胰腺脂肪坏死伴无症状急性胰腺炎及胆道狭窄:一例误诊病例分析
Authors Chen X , Luo Z, Xu J , Li C , Xu Y
Received 24 April 2025
Accepted for publication 15 August 2025
Published 23 August 2025 Volume 2025:18 Pages 1999—2003
DOI https://doi.org/10.2147/CCID.S535196
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Jeffrey Weinberg
Xiaofeng Chen,1 Zhuofu Luo,2 Jixiang Xu,3 Changqiang Li,1 Yang Xu1,3
1Department of Dermatology, The Fourth Affiliated Hospital of Southwest Medical University, Meishan, Sichuan, 620000, People’s Republic of China; 2Department of Dermatology, The First People’s Hospital of Shuangliu District, Chengdu, Sichuan, 610200, People’s Republic of China; 3Department of Dermatology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, 646000, People’s Republic of China
Correspondence: Yang Xu, Email xxff2007@163.com Changqiang Li, Email lcq-1973@163.com
Abstract: This report describes a case of pancreatic panniculitis secondary to acute pancreatitis caused by biliary stricture following multiple biliary surgeries. The aim is to highlight the importance of recognizing atypical presentations. The patient, a 46-year-old woman, presented with erythematous macules and nodules on the extremities accompanied by polyarthralgia. She had a history of multiple biliary surgeries over the past decade. Histopathological examination of the skin lesions revealed no significant epidermal abnormalities but demonstrated perivascular neutrophilic infiltration in the dermis and subcutaneous fat, with evidence of adipocyte necrosis, calcification, and ghost cell formation. Laboratory findings indicated hyperamylasemia; however, the initial imaging did not suggest pancreatitis and there are no relevant clinical symptoms, which contributed to the misdiagnosis. This case underscores the need for heightened awareness of atypical clinical manifestations in pancreatic-related conditions.
Keywords: pancreatic panniculitis, acute pancreatitis, biliary stricture, hyperamylasemia