Survey of Ophthalmology
Volume 55, Issue 3 , Pages 247-255, May 2010

Orbital Involvement in Castleman Disease

  • Ioannis Venizelos, PhD

      Affiliations

    • Department of Pathology, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece
  • ,
  • Thomas G. Papathomas, MD

      Affiliations

    • Department of Pathology, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece
    • Corresponding Author InformationReprint address: Thomas G. Papathomas, MD, 12 Kerkiras Str. (Kalamaria), Thessaloniki, GR-55133, Greece.
  • ,
  • Maria Papathanasiou, MD

      Affiliations

    • Hematology Section, 2nd Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece
  • ,
  • Angeliki Cheva, MD

      Affiliations

    • Department of Pathology, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece
  • ,
  • Vasilia Garypidou, PhD

      Affiliations

    • Hematology Section, 2nd Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece
  • ,
  • Sarah Coupland, MBBS, PhD, FRCPath

      Affiliations

    • Department of Cellular and Molecular Pathology, Royal Liverpool University Hospital, Liverpool, UK

published online 13 January 2010.

Stefan Seregard and Milton Boniuk, Editors

Abstract 

Castleman disease is a quite uncommon lymphoproliferative disorder usually occurring in the lymph nodes. Rarely, Castleman disease develops in an extranodal anatomic location. We report on the first biopsy-proven case of multicentric plasma cell type of Castleman disease involving the orbital areas in a human herpes virus 8 (HHV-8)-unassociated/ human immunodeficiency virus (HIV)-seronegative 70-year-old man suffering from Parkinson disease. The diagnosis was established on the basis of morphologic, immunophenotypic, and molecular findings of a lymph node and orbital soft tissue biopsy. We additionally provide a review of all previously published cases of Castleman disease with an orbital involvement, discussing the distinctive characteristics and potential associations with regard to their counterparts at other sites. Although Castleman disease involving the orbit is an exceptionally rare occurrence that may present initially with ocular signs and symptoms, this should be included in the complete differential diagnosis of orbital mass lesion.

Key words: Castleman disease, HHV8, multicentric, orbit, plasma cell variant

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 The authors reported no proprietary or commercial interest in any product mentioned or concept discussed in this article.

PII: S0039-6257(09)00262-8

doi:10.1016/j.survophthal.2009.09.003

Survey of Ophthalmology
Volume 55, Issue 3 , Pages 247-255, May 2010