T. Heinz et al., SOFT-TISSUE FUNGAL-INFECTIONS - SURGICAL-MANAGEMENT OF 12 IMMUNOCOMPROMISED PATIENTS, Plastic and reconstructive surgery, 97(7), 1996, pp. 1391-1399
Isolated fungal soft-tissue infections are uncommon but may cause seve
re morbidity or mortality among transplant recipients and other immuno
suppressed patients. Twelve immunocompromised patients illustrating th
ree patterns of infection were treated recently at the Duke University
Medical Center. These groups comprised (I) locally aggressive infecti
ons, (II) indolent infections, and (In) cutaneous manifestations of sy
stemic infection. Patient diagnoses included organ transplant, leukemi
a, prematurity, chronic obstructive pulmonary disease, and rheumatoid
arthritis. Time from immunosuppression to biopsy ranged from 5.5 to 31
weeks. Organisms included Aspergillus, Rhizopus, Fusarium, Paecilomyc
es, Exophiala, and Curvularia. Patients presented with necrotic ulcera
tions or nodules. Surgical treatment ranged from radical debridement t
o excisional biopsy to none. Antifungal chemotherapy also was employed
in some cases. The mortality rate was 33 percent, two patients dying
without evidence of fungal infection. Six of the eight survivors clear
ed their infections. Necrotic skin lesions with surrounding erythema i
n this population call for prompt examination, biopsy, and culture. Gr
oup I lesions mandate radical excision with rapid intraoperative micro
scopic control and systemic antifungal medication. Group II requires s
urgical control with or without antifungal therapy. Group III requires
systemic antifungal therapy for metastatic infection. In our opinion,
treatment of fungal soft-tissue infection should be tailored to infec
tion type and requires a team approach of surgeon and expert infectiou
s disease consultation.