Renal involvement as a unique manifestation of hemophagocytic syndrome
Renal-limited hemophagocytic syndrome (HPS) is a rare clinical setting characterized by abnormal activation of the immune system. Fever associated with pancytopenia, hepatosplenomegaly with liver dysfunction, and hypofibrinogenemia are usually observed in HPS. From a histological level, the presence...
Main Authors: | Dario Roccatello, Savino Sciascia, Antonella Barreca, Carla Naretto, Mirella Alpa, Giacomo Quattrocchio, Massimo Radin, Roberta Fenoglio |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-10-01
|
Series: | Frontiers in Medicine |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fmed.2022.796121/full |
Similar Items
-
Secondary hemophagocytic lymphohistiocytosis syndrome in adults: A case series and review of the literature
by: Rabab Taha, et al.
Published: (2017-01-01) -
Hemophagocytic lymphohistiocytosis associated with anaplasmosis
by: Tamara M Johnson, et al.
Published: (2017-01-01) -
Hemophagocytic lymphohistiocytosis: a case series analysis in a pediatric hospital
by: Itallo Oliveira Santos, et al.
Published: (2023-01-01) -
Hemophagocytic syndrome: a dilemma chasing the intensivists
by: Adriana Façanha Queiroz, et al.
Published: (2015-03-01) -
Hemophagocytic lymphohistiocytosis secondary to visceral leishmaniasis in an endemic area in the north of Minas Gerais, Brazil
by: Fernando Henrique Guimarães de Carvalho, et al.
Published: (2020-06-01)