Fang Li-Hua, Shih Li-Sun, Lee Pei-Ing, Chen Wei-Ting, Chen Rong-Long
From the Department of Pharmacy, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan (L-HF); Department of Pathology, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan (L-SH); Department of Nuclear Medicine, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan (P-IL); Department of Internal Medicine, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan (W-TC); and Department of Pediatric Hematology and Oncology, Koo Foundation Sun Yat-Sen Cancer Center, Taipei, Taiwan (R-LC).
Medicine (Baltimore). 2016 Jan;95(2):e2515. doi: 10.1097/MD.0000000000002515.
Mediastinal nonseminomatous germ cell tumor (MNSGCT)-associated histiocytic proliferations are rare and rapidly fatal disorders. Standard treatment modalities have yet to be established.We report a case of MNSGCT-associated hemophagocytic syndrome that evolved into malignant histiocytosis/disseminated histiocytic sarcoma (MH/HS), which was initially treated with intravenous immunoglobulin, corticosteroids, and cyclosporine. Then, thalidomide plus cyclophosphamide, adriamycin, oncovin, prednisolone chemotherapy followed by alemtuzumab-containing reduced-intensity allogeneic peripheral blood stem cell transplantation (PBSCT) was used as salvage therapy.The severe constitutional symptoms and pancytopenia resolved shortly after thalidomide with cyclophosphamide, adriamycin, oncovin, prednisolone. After PBSCT, the patient developed steroid-dependent skin graft-versus-host disease, but maintained a functional life for 1.5 years. Rapid resolution of chronic graft-versus-host disease preceded the fulminant recurrence of hemophagocytic syndrome and MH/HS.Thalidomide plus chemotherapy followed by alemtuzumab-containing reduced intensity allogeneic PBSCT is effective in allaying MNSGCT-associated histiocytic disorders, but does not prevent eventual relapse. However, further posttransplant immune modulation should be developed to completely eradicate the residual MH/HS cells.
纵隔非精原细胞瘤性生殖细胞肿瘤(MNSGCT)相关的组织细胞增殖是罕见且迅速致命的疾病。标准治疗方式尚未确立。我们报告一例MNSGCT相关的噬血细胞综合征,其演变为恶性组织细胞增多症/播散性组织细胞肉瘤(MH/HS),最初采用静脉注射免疫球蛋白、皮质类固醇和环孢素进行治疗。然后,使用沙利度胺加环磷酰胺、阿霉素、长春新碱、泼尼松龙化疗,随后进行含阿仑单抗的减低强度异基因外周血干细胞移植(PBSCT)作为挽救治疗。在使用沙利度胺联合环磷酰胺、阿霉素、长春新碱、泼尼松龙后不久,严重的全身症状和全血细胞减少症得到缓解。PBSCT后,患者出现了依赖类固醇的皮肤移植物抗宿主病,但维持了1.5年的功能性生命。慢性移植物抗宿主病的快速缓解先于噬血细胞综合征和MH/HS的暴发性复发。沙利度胺加化疗随后进行含阿仑单抗的减低强度异基因PBSCT可有效缓解MNSGCT相关的组织细胞疾病,但不能预防最终复发。然而,应开发进一步的移植后免疫调节方法以彻底根除残留的MH/HS细胞。