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A case of B-cell lymphoma secondary to hemophagocytic syndrome
  • +2
  • Hao Xing,
  • Luyao Ma,
  • Longfei Wang,
  • Qian Zhang,
  • Zhenjing Jin
Hao Xing
The Second Hospital of Jilin University
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Luyao Ma
The Second Hospital of Jilin University
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Longfei Wang
The Second Hospital of Jilin University
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Qian Zhang
The Second Hospital of Jilin University
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Zhenjing Jin
The Second Hospital of Jilin University

Corresponding Author:[email protected]

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Abstract

Hemophagocytic syndrome (HPS), also known as hemophagocytic lymphohistiocytosis (HLH), is a group of syndromes in which multiple pathogenic factors lead to the proliferation of activated lymphocytes and histiocytes that secrete large amounts of inflammatory cytokines[[1]](#ref-0001).HLH is a multi-organ hyperinflammatory syndrome caused by the secretion of large amounts of inflammatory cytokines from
28 Jul 2023Submitted to Clinical Case Reports
07 Aug 2023Submission Checks Completed
07 Aug 2023Assigned to Editor
09 Aug 2023Reviewer(s) Assigned
30 Aug 2023Review(s) Completed, Editorial Evaluation Pending
03 Sep 2023Editorial Decision: Revise Minor
12 Sep 20231st Revision Received
13 Sep 2023Assigned to Editor
13 Sep 2023Submission Checks Completed
13 Sep 2023Review(s) Completed, Editorial Evaluation Pending
18 Sep 2023Editorial Decision: Revise Minor
19 Sep 20232nd Revision Received
19 Sep 2023Assigned to Editor
19 Sep 2023Submission Checks Completed
19 Sep 2023Review(s) Completed, Editorial Evaluation Pending
29 Sep 2023Editorial Decision: Accept