Nishikawara Mayuka, Kawakami Toru, Sakai Hitoshi, Kawakami Fumihiro, Nishina Sayaka, Uehara Takeshi, Ishida Fumihiro, Nakazawa Hideyuki
Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, Japan.
Department of Diagnostic Pathology, Shinshu University School of Medicine, Japan.
Intern Med. 2020 Jun 1;59(11):1437-1443. doi: 10.2169/internalmedicine.4085-19. Epub 2020 Mar 5.
Primary adrenal lymphoma (PAL) is rare and known to have a predilection for central nervous system (CNS) relapse. A 70-year-old man with a 2-year history of primary aldosteronism presented because of a fever. He was hypotensive, and his adrenal glands were unequivocally enlarged. PAL was diagnosed. Despite showing an initial response to immunochemotherapy, progressive paralysis ensued. Magnetic resonance imaging findings were negative, and rituximab was ineffective. His debilitated condition hindered further chemotherapy. A postmortem examination revealed lymphoma relapse in the systemic peripheral nerves. The sequential presentation of two rare lymphomas implies that PAL might have a predilection for not only the CNS but also peripheral nerves.
原发性肾上腺淋巴瘤(PAL)较为罕见,已知易发生中枢神经系统(CNS)复发。一名患有原发性醛固酮增多症2年的70岁男性因发热前来就诊。他血压低,肾上腺明显肿大。诊断为PAL。尽管最初对免疫化疗有反应,但随后出现进行性麻痹。磁共振成像检查结果为阴性,利妥昔单抗无效。他虚弱的状况阻碍了进一步的化疗。尸检显示全身周围神经有淋巴瘤复发。两种罕见淋巴瘤的相继出现表明,PAL可能不仅易发生于CNS,也易发生于周围神经。