Invasive mould infection, e. g. aspergillosis in the first place, is a
common infection in immunocompromised patients. The diagnosis of inva
sive mould infection is difficult in the absence of confirmation by ti
ssue biopsy and histological studies. Therefore, prevalence of invasiv
e mould infections at the School of Medicine of the Leipzig University
between 1992 and 1994 was investiated. The diagnosis of invasive moul
d infection was suspected on clinical, mycological, and radiological f
indings. The definitive diagnosis was obtained by identification of ch
aracteristic mould hyphae on stained smears, and/or positive culture,
and/or the detection of Aspergillus antigen (Pastorex) in serum, bronc
hial secretion, or bronchoalveolar fluid, and confirmed by histopathol
ogy. In altogether 21 patients the definitive diagnosis invasive mould
infection was recorded, among them 20 invasive aspergilloses. Underly
ing diseases were leukaemia (n=11), aplastic anaemia (n=2), non-Hodgki
n-lymphoma (n=1), systemic lupus erythematosus (n=1), kidney transplan
tation (n=1), peritonitis after Billroth II anastomosis (n=1), Polymya
lgia rheumatica (n=1), AIDS plus Burkitt lymphoma (n=1), glioblastoma
(n=1), and subarachnoid haemorrhage (n=1). As causative fungi were iso
lated: Aspergillus fumigatus (n=13), Aspergillus terreus (n=1), Asperg
illus flavus as rare simultaneous infection with the basidiomycete Cop
rinus spec. in a leukaemic patient (n=1), and the dematiaceous fungus
Scedosporium prolificans in an AIDS patient with Burkitt lymphoma (n=1
). In four patients the invasive mould infection as confirmed histopat
hologically without isolation and differentiation of the causative age
nt. Nineteen of the 21 patients with invasive mould infection died cor
responding to a mortality rate of 90 %.