ABSTRACT
Hemophagocytic Lymphohistiocytosis (HLH) is defined by bone marrow and organ infiltration by activated and nonmalignant macrophages, which phagocytose blood cells. Renal is not a common damaged organ and has been rarely reported in hemophagocytic syndrome. We first reported a 43-year-old man with HLH and Immunoglobulin A (IgA) nephropathy accompanied with fever, splenomegaly, cytopenia, hypertriglyceridemia, hypofibrinogenemia, and hyperferritin.
14 Aug, 2015
Disclaimer
Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.
e-Published: 13 Jul, 2015
Disclaimer
Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.
