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Frontiers of Medicine

ISSN 2095-0217

ISSN 2095-0225(Online)

CN 11-5983/R

Postal Subscription Code 80-967

2018 Impact Factor: 1.847

Front. Med.    2008, Vol. 2 Issue (2) : 191-194    https://doi.org/10.1007/s11684-008-0036-8
Autologous peripheral hematopoietic stem-cell transplantation in a patient with refractory pemphigus
SUN Ledong1, SUN Jing1, ZENG Kang1, MENG Fanyi1, DIAO Youtao1, XU Dan1, HUANG Liang1, ZHAO Jie1, Liu Qifa2
1.Department of Dermatology, Nan-fang Hospital, Southern Medical University; 2. ;
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Abstract The aim of this study is to explore the effectiveness of autologous peripheral hematopoietic stem-cell transplantation in the treatment of refractory pemphigus. A 35-year-old male patient presented with a 4-year history of recurrent bullae on his trunk and extremities. The diagnosis of pemphigus was made on the basis of the clinical, histologic and immunofluorescence findings. The patient had shown resistance to conventional therapy with glucocorticoid and immunosuppressive agents. Two months before admission, he complained of hip joint pain. X-ray and CT scan revealed aseptic necrosis of the femoral head. Stem-cell mobilization was achieved by treatment with cyclophosphamide, granulocyte colony-stimulating factor (G-CSF) and rituximab. Peripheral blood stem cells were collected via leukapheresis and cryopreserved for later use. Immunoablation was accomplished by using cyclophosphamide (200 mg/kg; divided into 50 mg/kg on days -5, -4, -3, and -2), antithymocyte globulin (ATG; 10 mg/kg; divided into 2.5 mg/kg on days -6, -5, -4, and -3), and rituximab (1200 mg/d; divided into 600 mg/d on days 0 and 7). Autologous peripheral hematopoietic stem cell transplantation was followed by reconstitution of the immune system which was monitored by flow cytometry. The glucocorticoid was withdrawn immediately after transplantation. The pemphigus titer turned negative 6 weeks after transplantation and remained negative. The patient was in complete drug-free remission with no evidence of residual clinical or serological activity of pemphigus during 1 year of follow-up. The patient’s response suggests that autologous peripheral hematopoietic stem cell transplantation may be a potential “cure” for refractory pemphigus. However, further studies are needed to evaluate the risk-benefit ratio of this approach in patients with pemphigus showing resistance to conventional therapy.
Issue Date: 05 June 2008
 Cite this article:   
SUN Jing,SUN Ledong,HUANG Liang, et al. Autologous peripheral hematopoietic stem-cell transplantation in a patient with refractory pemphigus[J]. Front. Med., 2008, 2(2): 191-194.
 URL:  
https://academic.hep.com.cn/fmd/EN/10.1007/s11684-008-0036-8
https://academic.hep.com.cn/fmd/EN/Y2008/V2/I2/191
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