Xanthogranuloma of bone: A challenging imitator of malignancy

Brittany J. Holmes, Shobha Castelino-Prabhu, Dorothy L. Rosenthal, Syed Z. Ali

Research output: Contribution to journalArticle

Abstract

Xanthogranulomatous disease of bone is exceptionally uncommon. Clinically, radiologically and pathologically, it is a great imitator of malignancy. While there are few reports on the surgical pathology of this rare entity, there is no published report on its cytopathologic characteristics. We report herein the case of a 44-year-old male who was evaluated at The Johns Hopkins Hospital for a 2.3-cm painful soft tissue mass present within the medullary canal of the distal tibia with destruction of the overlying cortex. A computed tomography-guided fine needle aspiration biopsy revealed abundant histiocytes and occasional giant cells in an inflammatory background. This was interpreted as a 'histiocyte-rich lesion,' and an excisional biopsy was recommended. Subsequent curettage was performed, and the histological material was diagnosed as 'xanthogranuloma of bone.' The rarity of xanthogranuloma of bone and its resemblance to the more common reactive and malignant bone neoplasms may present diagnostic challenges.

Original languageEnglish (US)
Pages (from-to)198-202
Number of pages5
JournalActa cytologica
Volume57
Issue number2
DOIs
StatePublished - 2013

Keywords

  • Bone
  • Cytopathology
  • Fine needle aspiration
  • Histiocytes
  • Xanthogranuloma

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Histology

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