Pancreatic panniculitis associated with acinar cell pancreatic carcinoma

J Cutan Med Surg. 2008 Jan-Feb;12(1):38-42. doi: 10.2310/7750.2007.00032.

Abstract

Background: Pancreatic panniculitis is a rare entity, occurring in less than 2% of patients with pancreatic disorders. Skin manifestations may precede the diagnosis of a pancreatic disease by many months. When treatable, correction of the underlying pancreatic disorder may lead to prompt resolution of the panniculitis.

Objective: We present the case of a 74-year-old-man with a history of chronic pancreatitis who presented with an acute onset of tender, nonulcerating nodules. The clinical and histologic features of pancreatic panniculitis are discussed, with a brief review of the differential diagnosis and clinical approach to panniculitis.

Conclusions: Pancreatic panniculitis is a recognizable clinical entity with characteristic histologic features that may resolve with treatment of the underlying pancreatic disorder. The algorithm-based clinical approach to panniculitis presented in this study is a practical tool designed to guide clinicians in ordering investigations and determining the appropriate management for patients presenting with subcutaneous nodules.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged
  • Algorithms
  • Carcinoma, Acinar Cell / complications
  • Carcinoma, Acinar Cell / diagnosis*
  • Diagnosis, Differential
  • Fatal Outcome
  • Humans
  • Leg
  • Male
  • Pancreatic Diseases / diagnosis*
  • Pancreatic Diseases / etiology
  • Pancreatic Neoplasms / complications
  • Pancreatic Neoplasms / diagnosis*
  • Panniculitis / diagnosis*
  • Panniculitis / etiology