Unusual Cause of Splenomagaly

H. Elkaoui
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Abstract

A 67-year-old man with a history of hypertension, presented with a 3-month history of fatigue, intermittent fever and abdominal pain over the left upper quadrant. Abdominal examination revealed a splenomegaly (4cm from costal arch), without any regional lymphadenopathy. The hemogram was normal and blood biochemistry did not show abnormalities. Abdominal sonography showed multiple hypoechoic splenic nodules. Abdominal CT revealed multiple hypodense splenic tumors, likely perisplenic lymphadenopathy, around the pancreatic tail and splenic hilum, involving the splenic vein (Figure 1). The patient underwent splenectomy, and perisplenic and peripancreatic lymphnode dissection (Figure 2). Pathology revealed malignant splenic marginal zone B-cell lymphoma (SMZL). After 6 cycles of R-CHOP*, the patient went into complete remission. SMZL is an indolent B cell malignancy, presents as an incidental finding or with symptoms of splenic enlargement [1,2]. Diagnosis is based on lymphocyte morphology, immunophenotype and marrow and /or splenic histology [2]. Therapeutic options include splenectomy and alkylating agents. The median survival is 10-13 years [3].
脾肿大的不寻常原因
67岁男性,高血压病史,3个月疲乏、间歇性发热、左上腹腹痛。腹部检查显示脾肿大(距肋弓4cm),未见局部淋巴结病变。血象正常,血生化未见异常。腹部超声显示多发低回声脾结节。腹部CT显示胰腺尾和脾门周围多发低密度脾肿瘤,可能为脾周淋巴结病变,累及脾静脉(图1)。患者行脾切除术,脾周和胰周淋巴结清扫(图2)。病理显示脾边缘区恶性b细胞淋巴瘤(SMZL)。经过6个周期的R-CHOP*治疗后,患者完全缓解。SMZL是一种惰性B细胞恶性肿瘤,表现为偶然发现或伴有脾肿大症状[1,2]。诊断基于淋巴细胞形态学、免疫表型、骨髓和/或脾脏组织学[2]。治疗选择包括脾切除术和烷基化剂。中位生存期为10-13年[3]。
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