Adkins J W, Shields J A, Shields C L, Eagle R C, Flanagan J C, Campanella P C
Ocular Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, PA, USA.
Int Ophthalmol. 1996;20(6):339-43. doi: 10.1007/BF00176888.
Plasmacytomas of the ocular and adnexal tissue are rare. The variation in their clinical manifestations and potential association with multiple myeloma are not well appreciated.
We reviewed the clinical features and laboratory data of five cases of plasmacytoma involving the eye and orbit.
Plasmacytomas involved the conjunctiva in one case, the orbit in three cases, and the iris in one case. Plasmacytoma was the solitary plasma cell neoplasm in a patient with a conjunctival lesion and another patient with an orbital lesion. Two other patients who developed plasmacytomas of the orbit and iris, respectively, had a known history of multiple myeloma. An orbital plasmacytoma preceded the onset of systemic plasma cell neoplasia in the final patient.
Plasmacytomas of the eye and orbit are rare. They may or may not be associated with multiple myeloma.
眼及附属器组织的浆细胞瘤罕见。其临床表现的多样性以及与多发性骨髓瘤的潜在关联尚未得到充分认识。
我们回顾了5例累及眼和眼眶的浆细胞瘤的临床特征及实验室数据。
浆细胞瘤累及结膜1例,眼眶3例,虹膜1例。1例结膜病变患者和1例眼眶病变患者的浆细胞瘤为孤立性浆细胞肿瘤。另外2例分别发生眼眶和虹膜浆细胞瘤的患者有已知的多发性骨髓瘤病史。最后1例患者眼眶浆细胞瘤先于系统性浆细胞肿瘤出现。
眼和眼眶的浆细胞瘤罕见。它们可能与多发性骨髓瘤有关,也可能无关。