نتایج جستجو برای: hepatosplenomegaly

تعداد نتایج: 1767  

Journal: :iranian journal of child neurology 0
shadab salehpour 1. associate professor of pediatric endocrinology and metabolism, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: salehpour sh. clinical manifestations of type 1 gaucher disease. iran j child neurol autumn 2012; 6:4 (suppl. 1):13-14. pls see pdf. refe r ences 1. beutler e, grabowski ga. gaucher disease. in: metabolic and molecular bases of inherited disease, scriver cr, beaudet al, sly ws, valle d (eds), mcgraw-hill, new york 2001: 3635. 2. cox tm, schofield jp.   gaucher’s diseas...

2011
Shona Wilson Birgitte J. Vennervald David W. Dunne

Chronic hepatosplenomegaly, which is known to have a complex aetiology, is common amongst children who reside in rural areas of sub-Saharan Africa. Two of the more common infectious agents of hepatosplenomegaly amongst these children are malarial infections and schistosomiasis. The historical view of hepatosplenomegaly associated with schistosomiasis is that it is caused by gross periportal fib...

Journal: :The Journal of infectious diseases 2003
Joseph K Mwatha Frances M Jones Gamal Mohamed Cynthia W A Naus Eleanor M Riley Anthony E Butterworth Gachuhi Kimani Curtis H Kariuki John H Ouma Davy Koech David W Dunne

Schoolchildren from 2 areas of Kenya, Kangundo and Kambu, have contrasting prevalences of hepatosplenomegaly, despite having similar prevalences and intensities of Schistosoma mansoni infection. However, in individual children, S. mansoni infection intensity is positively correlated with organomegaly. In a previous study, hepatosplenomegaly was associated with Th1-type anti-schistosome cytokine...

Journal: :Archives of pediatrics & adolescent medicine 2003
Jason M Kane Kara Schmidt James H Conway

Hepatosplenomegaly in a young child can be an ominous physical finding, potentially representing a metabolic, malignant, or infectious process. We present the case of a 5-month-old girl who had fever, hepatosplenomegaly, and hematologic abnormalities at the initial examination. This case demonstrates how a comprehensive understanding of the pathophysiologic characteristics of hepatosplenomegaly...

Journal: :South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2017
Ricardo Gonçalves Ruchika Meel

Acute lymphoblastic leukaemia (ALL) is rarely seen in pregnancy. Massive hepatosplenomegaly as a presentation of ALL has not been described previously in any patient population. A 30-year-old pregnant woman presented at 16 weeks' gestation with epistaxis, jaundice, diffuse abdominal pain and distension, massive hepatosplenomegaly and peripheral oedema. On the basis of blood tests, bone marrow b...

Journal: :Proceedings of the Royal Society of Medicine 1934

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