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A case of pulmonary arterial hypertension associated with adult hemophagocytic lymphohistiocytosis
Abstract. Hemophagocytic lymphohistiocytosis (HLH) is an aggressive, life-threatening syndrome of excessive immune activation. Presentation is most common among the pediatric population, and cases in adults are rare. The number of nonhematologic presentations described in relation to HLH has been gr...
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| Vydáno v: | Pulm Circ |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
University of Chicago Press
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5210061/ https://ncbi.nlm.nih.gov/pubmed/28090306 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1086/688490 |
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