Systemic Infections with Aspergillus Species in Patients with Hematological Malignancies: Current Serological and Molecular Diagnostic Approaches

2001 ◽  
Vol 24 (6) ◽  
pp. 531-536 ◽  
Author(s):  
D. Buchheidt ◽  
B. Spiess ◽  
R. Hehlmann
2004 ◽  
Vol 45 (3) ◽  
pp. 463-468 ◽  
Author(s):  
Dieter Buchheidt ◽  
Margit Hummel ◽  
Dietlind Schleiermacher ◽  
Birgit Spiess ◽  
Rüdiger Hehlmann

Author(s):  
S.B. Shivachandra ◽  
M.M. Chanda ◽  
J. Hiremath ◽  
R. Yogisharadhya ◽  
N.N. Mohanty ◽  
...  

1995 ◽  
Vol 70 (3) ◽  
pp. 135-141 ◽  
Author(s):  
M. Z�hlsdorf ◽  
M. Hesse ◽  
R. Schulten ◽  
J. van de Loo ◽  
M. von Eiff ◽  
...  

2011 ◽  
Vol 79 (4) ◽  
pp. 385-390 ◽  
Author(s):  
A Drousiotou ◽  
I DiMeo ◽  
R Mineri ◽  
Th Georgiou ◽  
G Stylianidou ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Guillaume Morel ◽  
Joy Mootien ◽  
Philippe Guiot ◽  
Khaldoun Kuteifan

TAFRO syndrome is a distinct idiopathic multicentric Castleman disease characterized by the association of thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly. We report the first case occurring in a Caucasian pregnant woman. At 34 weeks of gestation, our patient presented with all clinical and biological symptoms compatible with a TAFRO syndrome. Tough quick cesarean section was performed as symptoms got worse with onset of multiorgan failure requiring mechanical ventilation for acute respiratory distress, continuous renal replacement, and vasopressors. Nine days after ICU admission, steroid boluses were started and allowed spectacular clinical and biological improvement. As systemic inflammatory manifestations are important, TAFRO syndrome can be mistaken with severe autoimmune diseases, systemic infections, hematological malignancies, or hemophagocytic lymphohistiocytosis.


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