TY - JOUR
T1 - Systemic Sporotrichosis Treated with Itraconazole
AU - Winn, Richard E.
AU - Anderson, Judith
AU - Piper, John
AU - Aronson, Naomi E.
AU - Pluss, Jerry
N1 - Funding Information:
From the Department of Medicine, Fitzsimons Army Medical Center, Aurora, Colorado; the North Colorado Medical Center, Greeley, Colorado; the Department of Medicine, David Grant Medical Center, Travis Air Force Base, California; and the Infectious Diseases Section, William Beaumont Army Medical Center, El Paso, Texas
PY - 1993/8/1
Y1 - 1993/8/1
N2 - Amphotericin B is recommended for the treatment of systemic infection caused by Sporothrix schenckii. However, this agent is toxic, its use is frequently followed by relapse, and some isolates of S. schenckii are resistant. Recent studies suggest that newer azole compounds, such as itraconazole, are effective in cutaneous and lymphocutaneous sporotrichosis, but data on their efficacy in systemic infections are scarce. We used itraconazole in the sequential treatment of six patients with systemic sporotrichosis: three with bone and joint disease and three with disseminated infection manifested by subcutaneous nodules. In all six cases, symptoms and signs of infection improved, with resolution of subcutaneous nodules, normalization of imaging studies, cessation of wound drainage, and return of joint mobility and function. No toxicity was noted. One patient with disseminated infection had a relapse while receiving 100 mg of itraconazole daily. The average duration of follow-up was 18 months. Thus itraconazole appears promising for the treatment of systemic sporotrichosis. A dose of at least 200 mg/d appears to be needed to prevent relapse.
AB - Amphotericin B is recommended for the treatment of systemic infection caused by Sporothrix schenckii. However, this agent is toxic, its use is frequently followed by relapse, and some isolates of S. schenckii are resistant. Recent studies suggest that newer azole compounds, such as itraconazole, are effective in cutaneous and lymphocutaneous sporotrichosis, but data on their efficacy in systemic infections are scarce. We used itraconazole in the sequential treatment of six patients with systemic sporotrichosis: three with bone and joint disease and three with disseminated infection manifested by subcutaneous nodules. In all six cases, symptoms and signs of infection improved, with resolution of subcutaneous nodules, normalization of imaging studies, cessation of wound drainage, and return of joint mobility and function. No toxicity was noted. One patient with disseminated infection had a relapse while receiving 100 mg of itraconazole daily. The average duration of follow-up was 18 months. Thus itraconazole appears promising for the treatment of systemic sporotrichosis. A dose of at least 200 mg/d appears to be needed to prevent relapse.
UR - http://www.scopus.com/inward/record.url?scp=0027220360&partnerID=8YFLogxK
U2 - 10.1093/clinids/17.2.210
DO - 10.1093/clinids/17.2.210
M3 - Article
C2 - 8399869
AN - SCOPUS:0027220360
SN - 1058-4838
VL - 17
SP - 210
EP - 217
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 2
ER -