Results 1 to 10 of about 60,923 (241)

Chronic Hepatosplenomegaly in African School Children: A Common but Neglected Morbidity Associated with Schistosomiasis and Malaria

open access: yesPLoS Neglected Tropical Diseases, 2011
Chronic hepatosplenomegaly, which is known to have a complex aetiology, is common amongst children who reside in rural areas of sub-Saharan Africa.
Shona Wilson, Birgitte Jyding Vennervald
exaly   +2 more sources

Hepatosplenomegaly associated with chronic malaria exposure: evidence for a pro‐inflammatory mechanism exacerbated by schistosomiasis

open access: yesParasite Immunology, 2009
In sub‐Saharan Africa, chronic hepatosplenomegaly, with palpable firm/hard organ consistency, is common, particularly among school‐aged children.
Shona Wilson   +9 more
exaly   +2 more sources

Health implications of chronic hepatosplenomegaly in Kenyan school-aged children chronically exposed to malarial infections and Schistosoma mansoni

open access: yesTransactions of the Royal Society of Tropical Medicine and Hygiene, 2010
Hepatosplenomegaly among school-aged children in sub-Saharan Africa is highly prevalent. Two of the more common aetiological agents of hepatosplenomegaly, namely chronic exposure to malaria and Schistosoma mansoni infection, can result in similar ...
Shona Wilson   +2 more
exaly   +2 more sources

Hepatosplenomegaly and Pernicious Anaemia [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Sir, Pernicious anaemia (PA) is the end stage of atrophic gastritis which results in the loss of parietal cells in the fundus and body of the stomach. Loss of parietal cells is associated with the failure of intrinsic factor production and results in vitamin B12 deficiency and megaloblastic anaemia.
Turgay Ulas   +4 more
doaj   +3 more sources

An unusual case of hepatosplenomegaly [PDF]

open access: yesGut, 2005
A 21 year old Asian female presented to our clinic with impaired renal function (creatinine level 217 μmol/l). There was no history of note. Physical examination elicited hepatosplenomegaly. There were no other positive findings. Urine analysis was unremarkable. …
D, Joshi   +4 more
openaire   +3 more sources

The Spectrum of Clinical Manifestations of Serious Human Parvovirus B19 Infection in Children without any Underlying Diseases- A Case Series [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Human Parvovirus B19 causes mild to life-threatening illnesses, especially in immunosuppressed individuals. In the immunocompetent individuals, the severe spectrum of clinical manifestations of the virus infection is not widely known.
Subham Bhattacharya   +2 more
doaj   +1 more source

Hemophagocytic Lymphohistiocytosis Presenting as Neonatal Cholestasis: A Case Report [PDF]

open access: yesIranian Journal of Neonatology, 2023
Background:. Hemophagocytic lymphohistosis (HLH) is a life-threatening clinical syndrome that involves liver dysfunction and can range from mild dysfunction to severe fulminant insufficiency.
Raheleh Faramarzi   +4 more
doaj   +1 more source

Parvovirus b19-Induced Acute Hepatitis With Hepatosplenomegaly and Polyarthropathy

open access: yesCureus, 2022
Parvovirus B19 infection can present with myriads of clinical diseases and syndromes; hepatitis and polyarthropathy are a few of these examples. Parvovirus frequently affects children but this condition has also been reported in adults.
Ubaid Khan   +4 more
semanticscholar   +1 more source

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