“What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus

Macrophage activation syndrome (MAS) is a potentially fatal condition characterized by massive systemic inflammatory response in the setting of a myriad of systemic disorders such as autoimmune collagen vascular disease, infections, drug-induced, and malignancies. It falls under a group of disorders...

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Main Authors: J P Prathibha, Vivek Pai, P Ishwara Bhat
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2021-01-01
Series:Clinical Dermatology Review
Subjects:
Online Access:http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2021;volume=5;issue=2;spage=236;epage=239;aulast=
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author J P Prathibha
Vivek Pai
P Ishwara Bhat
author_facet J P Prathibha
Vivek Pai
P Ishwara Bhat
author_sort J P Prathibha
collection DOAJ
description Macrophage activation syndrome (MAS) is a potentially fatal condition characterized by massive systemic inflammatory response in the setting of a myriad of systemic disorders such as autoimmune collagen vascular disease, infections, drug-induced, and malignancies. It falls under a group of disorders known as hemophagocytic lymphohistiocytosis of which familial and acquired types have been described. Here, we report a case of acquired MAS secondary to acute systemic lupus erythematosus (SLE). Early diagnosis and timely intervention resulted in a favorable outcome.
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spelling doaj.art-31baaf2de1e04bb2a284129a004221cb2022-12-21T21:30:31ZengWolters Kluwer Medknow PublicationsClinical Dermatology Review2542-551X2542-55282021-01-015223623910.4103/CDR.CDR_87_20“What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosusJ P PrathibhaVivek PaiP Ishwara BhatMacrophage activation syndrome (MAS) is a potentially fatal condition characterized by massive systemic inflammatory response in the setting of a myriad of systemic disorders such as autoimmune collagen vascular disease, infections, drug-induced, and malignancies. It falls under a group of disorders known as hemophagocytic lymphohistiocytosis of which familial and acquired types have been described. Here, we report a case of acquired MAS secondary to acute systemic lupus erythematosus (SLE). Early diagnosis and timely intervention resulted in a favorable outcome.http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2021;volume=5;issue=2;spage=236;epage=239;aulast=hemophagocytic lymphohistiocytosismacrophage activation syndromesystemic lupus erythematosus (sle)
spellingShingle J P Prathibha
Vivek Pai
P Ishwara Bhat
“What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
Clinical Dermatology Review
hemophagocytic lymphohistiocytosis
macrophage activation syndrome
systemic lupus erythematosus (sle)
title “What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
title_full “What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
title_fullStr “What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
title_full_unstemmed “What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
title_short “What lies beneath” – macrophage activation syndrome unveiled systemic lupus erythematosus
title_sort what lies beneath macrophage activation syndrome unveiled systemic lupus erythematosus
topic hemophagocytic lymphohistiocytosis
macrophage activation syndrome
systemic lupus erythematosus (sle)
url http://www.cdriadvlkn.org/article.asp?issn=2542-551X;year=2021;volume=5;issue=2;spage=236;epage=239;aulast=
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