The hemophagocytic syndrome

Authors

  • Neidy Lili Iscano Cruz Universidad Nacional Autónoma de Honduras
  • Fernando Arturo Fajardo Leitzelar Hospital Escuela Universitario; Tegucigalpa,Honduras

DOI:

https://doi.org/10.5377/rmh.v86i3-4.12179

Keywords:

Bone marrow, Hemophagocytic Iymphohistiocytosis, Phagocytosis, Severity

Abstract

Background: The hemophagocytic syndrome (SH) is a syndrome of pathological immune activation, rare, little diagnosed, its importance lies in its severity, since they are very aggressive cases that evolve in a short time in a fulminating way, with a lethal multiorgan failure, before establish a diagnosis. They are found in all age groups, but in general it is more frequent in children. The purpose of the revision was to obtain information about this pathology, identify the condition in a timely manner and also administer an early and adequate treatment to improve patient survival. Methods: We carried out an exhaustive search of articles with less than 10 years of publication in the PubMed, Scielo, Elsevier, Scribd, Medigraphic databases. Development and conclusions: Although SH is difficult to identify due to nonspecific symptoms, if it is diagnosed and treated at the opportune moment, given its high morbidity and mortality, it will be possible to save many lives.

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Author Biographies

Neidy Lili Iscano Cruz, Universidad Nacional Autónoma de Honduras

Medicina General y cirugía

Fernando Arturo Fajardo Leitzelar, Hospital Escuela Universitario; Tegucigalpa,Honduras

Médico especialista en Nefrología

Published

2018-12-20

How to Cite

Iscano Cruz, N. L. ., & Fajardo Leitzelar, F. A. . (2018). The hemophagocytic syndrome. Revista Médica Hondureña, 86(3-4), 134–137. https://doi.org/10.5377/rmh.v86i3-4.12179

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Section

REVISIÓN BIBLIOGRÁFICA