Hematology Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo, 113-8677, Japan.
Allergy and Autoimmune Disease Division, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
Int J Hematol. 2009 Nov;90(4):532-536. doi: 10.1007/s12185-009-0428-9. Epub 2009 Oct 24.
We report the first case of Mikulicz's disease (MD) occurring 2 years after autologous peripheral blood stem cell transplantation (PBSCT) for multiple myeloma (MM). A 70-year-old man developed bilateral enlargement of parotid and submandibular glands. The patient had previously received 2 courses of autologous PBSCT for IgG-kappa type MM, and had been stable for 2 years. This salivary gland enlargement was initially felt to represent a recurrence of MM, since along with gland swelling, IgG was also elevated. However, repeated biopsy of the left submandibular gland revealed chronic sclerosing sialadenitis rather than plasmacytoma. Results of salivary gland scintigraphy, serological testing, and absence of sicca symptoms also supported the diagnosis of MD. Concurrently, the patient developed severe thrombocytopenia (0.8 x 10(4)/microl). Bone marrow biopsy showed abundant megakaryocytes, suggesting enhanced platelet destruction. After high-dose steroid and immunoglobulin therapy, the platelet count gradually returned to normal with complete resolution of the salivary gland enlargement. No apparent signs of MM recurrence were documented during these clinical events.
我们报告首例多发性骨髓瘤(MM)自体外周血干细胞移植(PBSCT)后 2 年发生的米库利茨病(MD)。一位 70 岁男性出现双侧腮腺和颌下腺肿大。该患者曾因 IgG-κ型 MM 接受过 2 个疗程的自体 PBSCT,病情稳定 2 年。由于腺体肿胀同时伴有 IgG 升高,最初认为这种唾液腺肿大是 MM 的复发。然而,对左颌下腺的重复活检显示为慢性硬化性涎腺炎而不是浆细胞瘤。唾液腺闪烁显像、血清学检测以及无干燥症状的结果也支持 MD 的诊断。同时,患者发生严重血小板减少症(0.8×10(4)/µl)。骨髓活检显示巨核细胞丰富,提示血小板破坏增强。在接受大剂量类固醇和免疫球蛋白治疗后,血小板计数逐渐恢复正常,唾液腺肿大完全消退。在这些临床事件期间,未发现 MM 复发的明显迹象。