Cavanna L, Civardi G, Vallisa D, Bertè R
I Divisione di Medicina Interna ed Ematologia, Ospedale Civile di Piacenza.
Ann Ital Med Int. 1999 Oct-Dec;14(4):298-301.
Primary localized adrenal non-Hodgkin's lymphomas are extremely rare. Only 28 observations have been reported so far, all with a very poor prognosis: a median survival of 12.5 weeks. The authors report the case of a 78-year-old male with primary non-Hodgkin's lymphoma of the right adrenal gland. Disease onset was characterized by severe autoimmune hemolytic anemia, and diagnosis was made by echo-guided biopsy. The patient was admitted to our Department with severe autoimmune hemolytic anemia; the hemoglobin value was 6.5 g/dL and both indirect and direct Coombs' tests were positive. Steroid treatment with methylprednisolone 2 mg/kg/day did not improve the hemolytic process. Abdominal ultrasound examination disclosed a right hypoechogenic suprarenal mass of 10 x 9 cm; imaging techniques such as computed tomography and magnetic resonance imaging were not useful in the etiologic diagnosis of the right suprarenal mass; fine needle aspiration and tissue-core biopsy revealed low-grade non-Hodgkin's lymphoma. Staging procedures, including clinical examination, total body computed tomography scan, bone-marrow biopsy, gallium scan, abdominal magnetic resonance imaging, did not disclose other sites of involvement and strongly supported a diagnosis of primary non-Hodgkin's lymphoma of the right adrenal gland. Hormone assays were within normal limits. The patient was treated with chemotherapy, cyclophosphamide-vincristine-prednisone regimen, with good regression of the adrenal mass after 6 courses, and normalization of hemoglobin level and negativity of Coombs' tests. The importance of this case lies in the very rare occurrence of this disease, its association with autoimmune hemolytic anemia, the diagnosis made by ultrasound-guided biopsy, and good response to treatment with respect to cases reported in the literature. The patient remains in clinical remission 12 months after onset of the disease.
原发性局限性肾上腺非霍奇金淋巴瘤极为罕见。迄今为止,仅报告了28例病例,所有病例预后都非常差:中位生存期为12.5周。作者报告了一例78岁男性原发性右肾上腺非霍奇金淋巴瘤病例。疾病发作的特征为严重的自身免疫性溶血性贫血,通过超声引导下活检确诊。该患者因严重的自身免疫性溶血性贫血入住我院;血红蛋白值为6.5 g/dL,间接和直接抗人球蛋白试验均呈阳性。使用甲泼尼龙2 mg/kg/天的类固醇治疗未能改善溶血过程。腹部超声检查发现右肾上腺有一个10×9 cm的低回声肿块;计算机断层扫描和磁共振成像等影像学技术对右肾上腺肿块的病因诊断没有帮助;细针穿刺和组织芯活检显示为低级别非霍奇金淋巴瘤。分期检查,包括临床检查、全身计算机断层扫描、骨髓活检、镓扫描、腹部磁共振成像,未发现其他受累部位,强烈支持原发性右肾上腺非霍奇金淋巴瘤的诊断。激素测定结果在正常范围内。该患者接受了环磷酰胺-长春新碱-泼尼松方案的化疗,6个疗程后肾上腺肿块明显缩小,血红蛋白水平恢复正常,抗人球蛋白试验转阴。该病例的重要性在于这种疾病极为罕见,其与自身免疫性溶血性贫血相关,通过超声引导下活检确诊,并且相对于文献报道的病例对治疗反应良好。该患者在疾病发作12个月后仍处于临床缓解状态。