Successful treatment of immune reconstitution inflammatory syndrome in Whipple's disease using thalidomide

2010 ◽  
Vol 60 (1) ◽  
pp. 79-82 ◽  
Author(s):  
Jean-Christophe Lagier ◽  
Florence Fenollar ◽  
Hubert Lepidi ◽  
Eric Liozon ◽  
Didier Raoult
2021 ◽  
Vol 14 (6) ◽  
pp. e243633
Author(s):  
Patrick Hofmann ◽  
Nina Durisch ◽  
Claudia Buetikofer ◽  
Birgit Maria Helmchen

We present the case of a 70-year-old woman with a history of seronegative arthritis, recurrent pleural effusion and weight loss. A prior lung biopsy had revealed non-caseating epithelioid cell granulomas without evidence for microbial organisms on special stains. Intestinal biopsy findings where suspicious for Whipple’s disease, which was confirmed by PCR testing, both on the intestinal and retrospectively on the lung tissue. Treatment with ceftriaxone resulted in clinical deterioration with fever, arthritis and recurrent pleuritis consistent with immune reconstitution inflammatory syndrome. Dose increase of glucocorticoids and therapy rotation to doxycycline and hydroxychloroquine resulted in rapid clinical improvement.


2013 ◽  
Vol 190 (5) ◽  
pp. 2354-2361 ◽  
Author(s):  
Verena Moos ◽  
Gerhard E. Feurle ◽  
Katina Schinnerling ◽  
Anika Geelhaar ◽  
Julian Friebel ◽  
...  

2015 ◽  
Vol 82 (2) ◽  
pp. 122-124 ◽  
Author(s):  
Marielle Vayssade ◽  
Anne Tournadre ◽  
Michel D’Incan ◽  
Martin Soubrier ◽  
Jean-Jacques Dubost

2016 ◽  
Vol 8 (4) ◽  
Author(s):  
Markela Pagonitsa Zorzou ◽  
Maria Chini ◽  
Athina Lioni ◽  
Georgios Tsekes ◽  
Thomas Nitsotolis ◽  
...  

Although the connection of [secondary hemophagocytic syndrome (sHS)] with HIV has been well documented, optimal treatment regimen is not well established. This is due not only to the rarity of the syndrome, but also to the heterogeneity of the involved population. Most cases are related to opportunistic infections or malignancies in advanced stage, but many cases are also related to seroconversion, in the primary infection setting. Moreover, in the [antiretroviral treatment (ART)] era, rare cases of ART-related sHS have been reported. In these, often fatal cases, an [immune reconstitution inflammatory syndrome (IRIS)] process is involved, posing a serious challenge to the treating physician. We hereby report a case of successful treatment of an HIV patient with primary effusion lymphoma who experienced sHS shortly after ART onset. Our patient, treated with high dose dexamethasone and gamma globulin, achieved complete remission. This case might hint possible therapeutic insights in the treatment of IRIS-related sHS.


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