Castleman's disease mimicking right adrenal neoplasm: a case report

Turk J Gastroenterol. 2011 Oct;22(5):551-4. doi: 10.4318/tjg.2011.0270.

Abstract

Castleman's disease usually manifests as a solitary mediastinal tumor and only rarely as an isolated retroperitoneal mass. This disorder is often undiagnosed or misdiagnosed. Thus, only very few patients have been reported and little information is available in the literature. The definitive diagnosis is based on postoperative pathological findings. We report a case of a 57-year-old female with a Castleman's tumor located superomedial to the upper pole of the right kidney that mimicked an adrenal neoplasm. The mass was surgically resected, and the histopathological diagnosis of the resected tissue was hyaline-vascular type of Castleman's disease. Although retroperitoneal Castleman's disease is rare, it should be considered in the differential diagnosis of retroperitoneal masses.

Publication types

  • Case Reports

MeSH terms

  • Adrenal Gland Neoplasms / diagnosis*
  • Castleman Disease / diagnosis*
  • Castleman Disease / surgery
  • Diagnosis, Differential
  • Female
  • Humans
  • Laparotomy
  • Magnetic Resonance Imaging
  • Middle Aged
  • Retroperitoneal Space
  • Tomography, X-Ray Computed