Immunoablative high-dose cyclophosphamide without stem cell rescue in a patient with pemphigus vulgaris

被引:35
作者
Hayag, MV [1 ]
Cohen, JA
Kerdel, FA
机构
[1] Univ Miami, Dept Dermatol & Cutaneous Surg, Coral Gables, FL 33124 USA
[2] Univ Miami, Div Hematol & Oncol, Dept Med, Coral Gables, FL 33124 USA
关键词
D O I
10.1067/mjd.2000.110397
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The use of ablative intravenous cyclophosphamide (50 mg/kg per day for 4 days) without stem cell rescue has been described in patients with refractory autoimmune diseases such as paraneoplastic pemphigus, systemic lupus erythematosus, and aplastic anemia. We describe a 33-year-old patient with pemphigus vulgaris recalcitrant to multiple therapies. The patient presented with numerous oral ulcerations, erosions, and hyperpigmented crusted plaques on his face, trunk, and arms. Findings of a skin biopsy and direct immunofluorescence were consistent with pemphigus vulgaris. The circulating pemphigus vulgaris autoantibodies were present at a titer of 1:640. The patient received immunoablative therapy (50 mg/kg of cyclophosphamide for a total of 4 days) and tolerated the regimen well. Complications such as thrombocytopenia and Pseudomonas septicemia were quickly treated. Four months after the 4-day therapy, his oral and skin lesions completely healed, and his pemphigus titers have decreased to zero. He is no longer receiving prednisone and no new lesions have developed. This provides further evidence that this regimen is relatively safe and provides a potential "cure" for refractory autoimmune diseases such as pemphigus vulgaris.
引用
收藏
页码:1065 / 1069
页数:5
相关论文
共 25 条
[1]   AZATHIOPRINE IN THE TREATMENT OF PEMPHIGUS VULGARIS - A LONG-TERM FOLLOW-UP [J].
ABERER, W ;
WOLFFSCHREINER, EC ;
STINGL, G ;
WOLFF, K .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1987, 16 (03) :527-533
[2]   Pemphigus vulgaris antigen (Desmoglein 3) is localized in the lower epidermis, the site of blister formation in patients [J].
Amagai, M ;
Koch, PJ ;
Nishikawa, T ;
Stanley, JR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (02) :351-355
[3]   INDUCTION OF PEMPHIGUS IN NEONATAL MICE BY PASSIVE TRANSFER OF IGG FROM PATIENTS WITH THE DISEASE [J].
ANHALT, GJ ;
LABIB, RS ;
VOORHEES, JJ ;
BEALS, TF ;
DIAZ, LA .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 306 (20) :1189-1196
[4]   PEMPHIGUS-VULGARIS AND PEMPHIGUS-VEGETANS [J].
BECKER, BA ;
GASPARI, AA .
DERMATOLOGIC CLINICS, 1993, 11 (03) :429-452
[5]   Complete remission in severe aplastic anemia after high-dose cyclophosphamide without bone marrow transplantation [J].
Brodsky, RA ;
Sensenbrenner, LL ;
Jones, RJ .
BLOOD, 1996, 87 (02) :491-494
[6]   Immunoablative high-dose cyclophosphamide without stem-cell rescue for refractory, severe autoimmune disease [J].
Brodsky, RA ;
Petri, M ;
Smith, BD ;
Seifter, EJ ;
Spivak, JL ;
Styler, M ;
Dang, CV ;
Brodsky, I ;
Jones, RJ .
ANNALS OF INTERNAL MEDICINE, 1998, 129 (12) :1031-1035
[7]   Mucosal and mucocutaneous (generalized) pemphigus vulgaris show distinct autoantibody profiles [J].
Ding, X ;
Aoki, V ;
Mascaro, JM ;
LopezSwiderski, A ;
Diaz, LA ;
Fairley, JA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1997, 109 (04) :592-596
[8]   Early recurrence or persistence of autoimmune diseases after unmanipulated autologous stem cell transplantation [J].
Euler, HH ;
Marmont, AM ;
Bacigalupo, A ;
Fastenrath, S ;
Dreger, P ;
Hoffknecht, M ;
Zander, AR ;
Schalke, B ;
Hahn, U ;
Haas, R ;
Schmitz, N .
BLOOD, 1996, 88 (09) :3621-3625
[9]   IDENTIFICATION OF PEMPHIGUS VULGARIS ANTIGEN EXTRACTED FROM NORMAL HUMAN-EPIDERMIS AND COMPARISON WITH PEMPHIGUS FOLIACEUS ANTIGEN [J].
EYRE, RW ;
STANLEY, JR .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (03) :807-812
[10]   THE CORRELATION OF DISEASE-ACTIVITY AND ANTIBODY-TITERS IN PEMPHIGUS [J].
FITZPATRICK, RE ;
NEWCOMER, VD .
ARCHIVES OF DERMATOLOGY, 1980, 116 (03) :285-290