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Light chain systemic amyloidosis manifested as liver failure complicated with fatal spontaneous splenic rupture: A case report
  • Li Duo,
  • Zhao Yingren,
  • Chen Hongmei
Li Duo
Xi'an Jiaotong University Medical College First Affiliated Hospital
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Zhao Yingren
Xi'an Jiaotong University Medical College First Affiliated Hospital
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Chen Hongmei
Xi'an Jiaotong University Medical College First Affiliated Hospital
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Abstract

Light chain systemic amyloidosis has low clinical incidence rate and poor prognosis. Relevant diagnosis depends on the biopsy results, and many patients were not confirmed until autopsy. Once amyloidosis is suspected, it is necessary to communicate with their families on the risks for treatment methods and prognosis.

Peer review status:IN REVISION

31 May 2021Submitted to Clinical Case Reports
07 Jun 2021Assigned to Editor
07 Jun 2021Submission Checks Completed
12 Jun 2021Reviewer(s) Assigned
06 Jul 2021Review(s) Completed, Editorial Evaluation Pending
13 Jul 2021Editorial Decision: Revise Minor