Article
Case Report: Hemophagocytic lymphohistiocytosis associated with acute polymyositis
2022-09-29
Abstract excerpt
Hemophagocytic lymphohistiocytosis (HLH) is a rare condition marked by uncontrolled histiocyte proliferation and activation, and phagocytosis of normal hematopoietic cells. This disease is rare, and a concurrent presentation with acute polymyositis is rare. A 14-year-old male was admitted to Chattogram Medical College Hospital with a high-grade fever for 25 days, generalized severe body aches, and multiple large j...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 228bddf2-7a71-5f71-bc73-e4f57cbbff66
- DOI
- 10.12688/f1000research.123220.1