Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.

BACKGROUND/PURPOSE:Hemophagocytic lymphohistiocytosis (HLH) is a rare, life threatening hyperinflammatory syndrome. Sinusoidal hemophagocytosis is occasionally observed on liver biopsy in patients who do not have clinical suspicion of HLH. We aimed at comparing the clinical characteristics and outco...

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Main Authors: Jacqueline De Gottardi, Matteo Montani, Anne Angelillo-Scherrer, Alicia Rovo, Annalisa Berzigotti
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0226899
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spelling doaj-22820bb2cbf247a2ba7adda8d4a83b862021-03-03T21:24:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011412e022689910.1371/journal.pone.0226899Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.Jacqueline De GottardiMatteo MontaniAnne Angelillo-ScherrerAlicia RovoAnnalisa BerzigottiBACKGROUND/PURPOSE:Hemophagocytic lymphohistiocytosis (HLH) is a rare, life threatening hyperinflammatory syndrome. Sinusoidal hemophagocytosis is occasionally observed on liver biopsy in patients who do not have clinical suspicion of HLH. We aimed at comparing the clinical characteristics and outcomes of patients with signs of hemophagocytosis on liver biopsy meeting and not meeting the HLH diagnostic criteria. METHODS:We reviewed the clinical, laboratory features and outcomes of all adult patients consecutively admitted in our center between 08/2011 and 08/2017 presenting with liver histology showing sinusoidal hemophagocytosis and of critically ill patients presenting with severe liver disease in whom hemophagocytosis was histologically confirmed. The characteristics of patients fulfilling and not fulfilling the diagnostic criteria of HLH were compared. RESULTS:We identified 12 cases (58% male, median age 61, 75% with a chronic underlying disease) with liver histology showing sinusoidal hemophagocytosis. All had at least some of the clinical features typically associated with HLH. Six were critical ill patients. In 4 cases with insufficient laboratory and clinical criteria, liver biopsy allowed to confirm the HLH diagnosis. Six patients died, of which four met the diagnostic criteria for HLH. Two patients with chronic liver disease died despite not fulfilling the diagnostic criteria of HLH. CONCLUSION:Hemophagocytosis on liver biopsy may contribute to confirming a diagnosis of HLH in suspected cases with indeterminate clinical and laboratory findings. Sinusoidal hemophagocytosis in patients with cirrhosis was associated with bad outcome.https://doi.org/10.1371/journal.pone.0226899
collection DOAJ
language English
format Article
sources DOAJ
author Jacqueline De Gottardi
Matteo Montani
Anne Angelillo-Scherrer
Alicia Rovo
Annalisa Berzigotti
spellingShingle Jacqueline De Gottardi
Matteo Montani
Anne Angelillo-Scherrer
Alicia Rovo
Annalisa Berzigotti
Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
PLoS ONE
author_facet Jacqueline De Gottardi
Matteo Montani
Anne Angelillo-Scherrer
Alicia Rovo
Annalisa Berzigotti
author_sort Jacqueline De Gottardi
title Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
title_short Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
title_full Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
title_fullStr Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
title_full_unstemmed Hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
title_sort hepatic sinusoidal hemophagocytosis with and without hemophagocytic lymphohistiocytosis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description BACKGROUND/PURPOSE:Hemophagocytic lymphohistiocytosis (HLH) is a rare, life threatening hyperinflammatory syndrome. Sinusoidal hemophagocytosis is occasionally observed on liver biopsy in patients who do not have clinical suspicion of HLH. We aimed at comparing the clinical characteristics and outcomes of patients with signs of hemophagocytosis on liver biopsy meeting and not meeting the HLH diagnostic criteria. METHODS:We reviewed the clinical, laboratory features and outcomes of all adult patients consecutively admitted in our center between 08/2011 and 08/2017 presenting with liver histology showing sinusoidal hemophagocytosis and of critically ill patients presenting with severe liver disease in whom hemophagocytosis was histologically confirmed. The characteristics of patients fulfilling and not fulfilling the diagnostic criteria of HLH were compared. RESULTS:We identified 12 cases (58% male, median age 61, 75% with a chronic underlying disease) with liver histology showing sinusoidal hemophagocytosis. All had at least some of the clinical features typically associated with HLH. Six were critical ill patients. In 4 cases with insufficient laboratory and clinical criteria, liver biopsy allowed to confirm the HLH diagnosis. Six patients died, of which four met the diagnostic criteria for HLH. Two patients with chronic liver disease died despite not fulfilling the diagnostic criteria of HLH. CONCLUSION:Hemophagocytosis on liver biopsy may contribute to confirming a diagnosis of HLH in suspected cases with indeterminate clinical and laboratory findings. Sinusoidal hemophagocytosis in patients with cirrhosis was associated with bad outcome.
url https://doi.org/10.1371/journal.pone.0226899
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