Department of Pathology, Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece.
Surv Ophthalmol. 2010 May-Jun;55(3):247-55. doi: 10.1016/j.survophthal.2009.09.003. Epub 2010 Jan 13.
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.
血管滤泡性淋巴结增生症是一种罕见的淋巴组织增生性疾病,通常发生在淋巴结。血管滤泡性淋巴结增生症很少发生在结外解剖部位。我们报告首例经活检证实的多中心浆细胞型血管滤泡性淋巴结增生症,发生在一名 70 岁的人类疱疹病毒 8(HHV-8)阴性/人类免疫缺陷病毒(HIV)阴性的帕金森病患者的眼眶区域。该诊断基于淋巴结和眼眶软组织活检的形态学、免疫表型和分子研究结果。我们还回顾了所有以前报道的眼眶受累的血管滤泡性淋巴结增生症病例,讨论了其与其他部位相应病例的特征和潜在关联。虽然眼眶受累的血管滤泡性淋巴结增生症极为罕见,最初可能表现为眼部体征和症状,但这应包括在眼眶肿块病变的完整鉴别诊断中。