Manganelli P, Fietta P, Quaini F
Unità Operativa di Reumatologia e Medicina Interna, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
Clin Exp Rheumatol. 2006 Jul-Aug;24(4):438-48.
Sjögren's syndrome (SS) is a chronic autoimmune disorder, primarily characterized by the mononuclear cell infiltration of exocrine glands exiting in parenchymal damage and secretory impairment. The spectrum of the disease extends from an autoimmune exocrinopathy to a systemic process with extraglandular manifestations. SS is defined as primary (pSS) when isolated, or secondary when associated with another autoimmune disease. Patients with pSS may present hematologic abnormalities, such as anemia, hemocytopenias, monoclonal gammopathies and lymphoprolipherative disorders, predominantly non-Hodgkin's lymphoma of B-cell origin. The increased prevalence of B-cell malignancies suggests that SS may be a boundary disease between autoimmunity and lymphoproliferation. In this paper, the hematologic manifestations of pSS are reviewed.
干燥综合征(SS)是一种慢性自身免疫性疾病,主要特征为外分泌腺的单核细胞浸润,进而导致实质损伤和分泌功能障碍。该疾病范围从自身免疫性外分泌病扩展至伴有腺体外表现的全身性疾病。SS若单独出现则定义为原发性干燥综合征(pSS),若与另一种自身免疫性疾病相关则为继发性干燥综合征。pSS患者可能出现血液学异常,如贫血、血细胞减少、单克隆丙种球蛋白病和淋巴增殖性疾病,主要是B细胞起源的非霍奇金淋巴瘤。B细胞恶性肿瘤患病率的增加表明SS可能是自身免疫和淋巴增殖之间的交界性疾病。本文对pSS的血液学表现进行综述。