Stroehmann Arne, Dörner Thomas, Lukowsky Ansgar, Feist Eugen, Hiepe Falk, Burmester Gerd-Rüdiger
Department of Anaesthesiology and Intensive Care Medicine, Charité University Hospital, Humboldt University, Berlin, Germany.
J Rheumatol. 2002 Jun;29(6):1326-9.
We describe a patient with primary biliary cirrhosis (PBC) and secondary Sjogren's syndrome (SS) with pulmonary involvement who developed a cutaneous T cell lymphoma. The clinical course of secondary SS in PBC is thought to be less complicated than in progressive systemic scleroderma and SS. In contrast to secondary SS, the risk for developing non-Hodgkin's lymphoma is highly increased in patients with primary SS. Moreover, these lymphomas are usually of B cell origin. There are few reports of T cell lymphoma in primary SS. The occurrence of a T cell lymphoma in a patient with PBC and secondary SS indicates the necessity to investigate lymphoma in patients with secondary SS.
我们描述了一名患有原发性胆汁性肝硬化(PBC)和继发性干燥综合征(SS)且有肺部受累的患者,该患者发生了皮肤T细胞淋巴瘤。PBC患者继发性SS的临床病程被认为比进行性系统性硬化症和SS患者的临床病程并发症更少。与继发性SS相反,原发性SS患者发生非霍奇金淋巴瘤的风险显著增加。此外,这些淋巴瘤通常起源于B细胞。原发性SS患者发生T细胞淋巴瘤的报道很少。一名PBC和继发性SS患者发生T细胞淋巴瘤表明有必要对继发性SS患者进行淋巴瘤调查。