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Autor:
Abinaya Srinivasa Rangan, Nithesh Babu Ramesh, Keesari Sai Sandeep Reddy, Raghunathan E. G., Prasanna Karthik Suthakaran
Publikováno v:
Romanian Journal of Rheumatology, Vol 33, Iss 3, Pp 191-196 (2024)
Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening multisystem disorder characterized by immune system dysregulation, hypercytokinemia, and hyperinflammation. This excessive inflammatory response is triggered by the uncontrolled
Externí odkaz:
https://doaj.org/article/25e841c6236a464c86bbd3081f877caa