Hemophagocytic lymphohistiocytosis differential diagnosis: Difference between revisions
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==Overview== | ==Overview== | ||
==Differentiating Hemophagocytic | ==Differentiating Hemophagocytic lymphohistiocytosis from other Diseases== | ||
The differential diagnosis of familial hemophagocytic lymphohistiocytosis includes | The differential diagnosis of familial hemophagocytic lymphohistiocytosis includes | ||
* Secondary HLH | * Secondary HLH | ||
* [[Macrophage-activation syndrome]] | * [[Macrophage-activation syndrome]] | ||
* Other primary immunodeficiencies that present with hemophagocytic lymphohistiocytosis, such as [[X-linked lymphoproliferative disease]]. | * Other primary immunodeficiencies that present with hemophagocytic lymphohistiocytosis, such as [[X-linked lymphoproliferative disease]]. | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 13:49, 21 September 2012
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Differentiating Hemophagocytic lymphohistiocytosis from other Diseases
The differential diagnosis of familial hemophagocytic lymphohistiocytosis includes
- Secondary HLH
- Macrophage-activation syndrome
- Other primary immunodeficiencies that present with hemophagocytic lymphohistiocytosis, such as X-linked lymphoproliferative disease.