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Adrenal cystic lesions: A clinicopathological analysis of 25 cases with proposed histogenesis and review of the literature

  • Hui Ping Chien
  • , Yu Sun Chang
  • , Pei Sung Hsu
  • , Jen Der Lin
  • , Yi Chin Wu
  • , Hui Lang Chang
  • , Cheng Keng Chuang
  • , Ke Hung Tsuei
  • , Chuen Hsueh*
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital
  • Shin Kong Wu Ho-Su Memorial Hospital
  • Chang Gung University

Research output: Contribution to journalReview articlepeer-review

62 Scopus citations

Abstract

Adrenal cystic lesions are uncommon and we analyzed clinical and pathologic features of 25 such cases from a single institute over 23 years. There were 16 pseudocysts, eight endothelial cysts, and one epithelial cyst. Seven of eight endothelial cysts were confirmed to be lymphangiomatous by D2-40 immunostaining. We suggest that pseudocysts and endothelial cysts may have different histogenesis. The proposed mesothelial origin of adrenal epithelial cyst cannot be confirmed in our example. Seven adrenal pseudocysts were associated with tumor, including two pheochromocytomas, one neuroblastoma, one adrenal cortical carcinoma, one adrenal cortical adenoma, one myelolipoma, and one schwannoma. The distinction of true cystic lesion from cystic neoplasm is important and requires thorough sampling of the specimens.

Original languageEnglish
Pages (from-to)274-281
Number of pages8
JournalEndocrine Pathology
Volume19
Issue number4
DOIs
StatePublished - 12 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adrenal cystic lesions
  • D2-40
  • Endothelial cyst
  • Epithelial cyst immunohistochemistry
  • Pseudocyst

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