Adult-Onset Still’s Disease Complicated with Haemophagocytic Lymphohistiocytosis (HLH): A Case Report

Adult-Onset Still’s Disease Complicated with Haemophagocytic Lymphohistiocytosis (HLH): A Case Report

Haemophagocytic lymphohistiocytosis (HLH) is a rare but potentially aggressive and life-threatening syndrome of overactive histiocytes and lymphocytes that commonly affects infants; it is also observed in children and adults of all ages. The disease is differentiated into either primary or secondary...

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Bibliographic Details
Main Authors: Muhammad Sohaib Asghar, Abubakar Tauseef, Warda Fatmi, Narmin Khan, Maryam Zafar, Uzma Rasheed, Nimra Shaikh, Mohammed Akram, Basmah Fayaz, Zehra Iqbal
Format: Article
Language:English
Published: European Medical Journal 2020-07-01
Series:European Medical Journal Hematology
Subjects:
adult-onset still’s disease
autoimmune
connective tissue
haematology
haemophagocytic lymphohistiocytosis (hlh)
immunology
infectious diseases
macrophage activation syndrome
rheumatology
Online Access:https://www.emjreviews.com/hematology/article/adult-onset-stills-disease-complicated-with-haemophagocytic-lymphohistiocytosis-hlh-a-case-report/

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https://www.emjreviews.com/hematology/article/adult-onset-stills-disease-complicated-with-haemophagocytic-lymphohistiocytosis-hlh-a-case-report/

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