Toubai Tomomi, Akama Hiroyoshi, Takagawa Masanori, Ishida Shuichi, Kasai Masaharu, Tanaka Junji, Imamura Masahiro
Department of Internal Medicine, Ishinomaki Red Cross Hospital.
Rinsho Ketsueki. 2002 Sep;43(9):851-6.
A 78-year-old male was admitted to our hospital complaining of nausea, general fatigue and anorexia in November, 1999. Clinical findings on admission were weight loss and dehydration but surface lymph nodes were not palpable. Masses in the bilateral adrenal glands were detected by ultrasonography, computed tomography and magnetic resonance imaging. Laboratory examinations revealed hyponatremia and hyperkalemia. Subsequent endocrine function tests showed normal serum cortisol and increased adrenocorticotropic hormone (ACTH) levels. Rapid ACTH test and cortico-hormone releasing hormone (CRH) test revealed insufficient secretion of cortisol. The histological diagnosis of the adrenal gland by laparotomy was diffuse large B-cell lymphoma. We diagnosed primary adrenal lymphoma with adrenal insufficiency. The patient underwent hormone supplementary therapy and chemotherapy, but he died two months later. We report on this rare primary adrenal lymphoma case and summarize the reports of this disease in the Japanese literature.
一名78岁男性于1999年11月因恶心、全身乏力和厌食入住我院。入院时的临床检查发现体重减轻和脱水,但未触及浅表淋巴结。通过超声、计算机断层扫描和磁共振成像检测到双侧肾上腺有肿块。实验室检查显示低钠血症和高钾血症。随后的内分泌功能测试显示血清皮质醇正常,促肾上腺皮质激素(ACTH)水平升高。快速ACTH试验和促肾上腺皮质激素释放激素(CRH)试验显示皮质醇分泌不足。经剖腹手术对肾上腺进行组织学诊断为弥漫性大B细胞淋巴瘤。我们诊断为原发性肾上腺淋巴瘤伴肾上腺功能不全。患者接受了激素补充治疗和化疗,但两个月后死亡。我们报告了这例罕见的原发性肾上腺淋巴瘤病例,并总结了日本文献中关于该病的报道。