R. Grobholz et al., Fatal Aspergillus fumigatus septicemia in a patient with an ectopic ACTH-producing neuroendocrine pancreatic tumor, ENDOCR PATH, 10(2), 1999, pp. 181-185
The case of a 71-yr-old Caucasian patient who suffered from an adrenocortic
otropic hormone (ACTH)-producing tumor and developed a fulminant Aspergillu
s fumigatus septicemia is reported. The patient presented initially with a
recent onset of hyperglycemia and had excessive plasma levels of cortisol a
nd ACTH. A computer-assisted tomography scan showed a tumor associated with
in the head of the pancreas. During his hospital course, he developed a rap
id progressive fatal Aspergillus fumigatus pneumonia and an upper gastroint
estinal bleeding. At necropsy multiple abscesses in the brain, lungs, heart
, kidneys, small bowel and mesentery were present as a result of Aspergillu
s septicemia. A neuroendocrine pancreatic tumor, 8 cm in diameter, was foun
d in the head of the pancreas without any signs of malignancy. The tumor sh
owed immunohistochemical and electron microscopic evidence of ACTH expressi
on, but of no other pituitary or pancreatic hormones. This case demonstrate
s the fulminant progress of a septicemia based on an immunologically compro
mised patient because of ectopic Gushing's syndrome. Early diagnosis of ect
opic ACTH syndromes is essential for adequate therapy in order to prevent c
omplications and fatal infections.