2018
DOI: 10.1016/j.bcmd.2017.04.008
|View full text |Cite
|
Sign up to set email alerts
|

Resolution of a steroid-resistant, hypereosinophilic immune diathesis with mepolizumab and concomitant amelioration of a mixed thrombotic microangiopathy

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2018
2018
2018
2018

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 41 publications
0
2
0
Order By: Relevance
“…Mepolizumab improved disease course in a patient with atypical hemolytic uremic syndrome (aHUS), who responded poorly to eculizumab (anti-C5a) alone ( 92 ). Monthly mepolizumab injections were initiated because of associated blood and tissue (colon) eosinophilia, resulting in normalization of eosinophil and platelet counts, increased ADAMTS13 activity, and regression of digestive and neurological manifestations.…”
Section: Anti-il-5 Treatment In Other Inflammatory Disorders Associatmentioning
confidence: 99%
“…Mepolizumab improved disease course in a patient with atypical hemolytic uremic syndrome (aHUS), who responded poorly to eculizumab (anti-C5a) alone ( 92 ). Monthly mepolizumab injections were initiated because of associated blood and tissue (colon) eosinophilia, resulting in normalization of eosinophil and platelet counts, increased ADAMTS13 activity, and regression of digestive and neurological manifestations.…”
Section: Anti-il-5 Treatment In Other Inflammatory Disorders Associatmentioning
confidence: 99%
“…Low evidence exists for an association of PBE and thrombotic microangiopathies (TMA). Eight reported cases of TMA with PBE were diagnosed as HES [17,102,103,104,105,106]. Recently, one case of atypical HUS with AIN and PBE was reported and the first two case reports of concomitant atypical HUS and EGPA were published [107,108].…”
Section: Eosinophilia In Kidney Diseasementioning
confidence: 99%