William Basem M, Harbert Tracey, Ganti Apar K, Bierman Philip J
University of Nebraska Medical Center and Omaha Veterans Affairs Medical Center, Omaha, Nebraska 68198-7680, USA.
Hematol Oncol Stem Cell Ther. 2011;4(3):132-5. doi: 10.5144/1658-3876.2011.132.
We report a case of a 61-year-old man with a history of CREST syndrome (calcinosis cutis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) who presented for evaluation of thrombocytopenia. He had evident cervical adenopathy and lymph node biopsy showed small lymphocytic lymphoma (SLL) with evident systemic adenopathy and bone marrow involvement. The patient achieved a complete remission with FCR (fludarabine/cyclophosphamide/rituximab) chemotherapy. About 30 cases of lymphomas are reported in the literature in association with systemic sclerosis. To our knowledge, there are no reports of a small lymphocytic lymphoma (SLL) in association with limited cutaneous systemic sclerosis with classic features of the CREST syndrome.
我们报告一例61岁男性患者,有CREST综合征(皮肤钙质沉着、雷诺现象、食管动力障碍、指端硬化和毛细血管扩张)病史,因血小板减少前来评估。他有明显的颈部淋巴结肿大,淋巴结活检显示为小淋巴细胞淋巴瘤(SLL),伴有明显的全身淋巴结肿大和骨髓受累。该患者接受FCR(氟达拉滨/环磷酰胺/利妥昔单抗)化疗后达到完全缓解。文献报道约有30例淋巴瘤与系统性硬化症相关。据我们所知,尚无关于伴有CREST综合征典型特征的局限性皮肤系统性硬化症相关的小淋巴细胞淋巴瘤(SLL)的报道。