Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
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Target Concepts:
Gene/Protein
Disease
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Query: UMLS:C0019209 (
hepatomegaly
)
5,798
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
We evaluated praziquantel for therapy of active Schistosoma mansoni infection in 15 rural Egyptian males with hepatosplenic schistosomiasis. Criteria for inclusion in this study were two pre-treatment S. mansoni egg counts with a mean of greater than 100 eggs g-1 faeces and an enlarged spleen. Fourteen of 15 patients had
hepatomegaly
, five had ascites, and six had serum albumin below 3 g dl-1.
Schistosoma haematobium infection
(less than 10 eggs ml-1 urine) was present in three patients. Praziquantel was administered in a single oral dose of 30 mg kg-1 body weight. Eight of the 15 patients (53%) had mild and transient reactions in the form of fever (usually one day), gastrointestinal symptoms, headache and skin rash. Criteria for parasitological cure were the absence of live eggs in two stool samples and a negative rectal snip biopsy three months after therapy. Ten patients ceased to pass live eggs (cure rate 67%). For the five who were still passing live eggs there was a mean egg reduction of 95%. The three patients with S. haematobium demonstrated parasitological cures. We conclude that praziquantel is an effective and well tolerated drug for treatment of S. mansoni infection in patients with advanced hepatosplenic schistosomiasis, and it is the drug of choice for patients with coexisting S. haematobium infection.
...
PMID:Praziquantel for treatment of schistosomiasis in patients with advanced hepatosplenomegaly. 393 36
During a study in Kenya of the relationships between
Schistosoma haematobium infection
and anemia and growth, evidence was found to suggest that this infection was associated with splenomegaly in children, and that both splenomegaly and
hepatomegaly
regressed in children treated for urinary schistosomiasis, compared with a placebo group. These results imply that S. haematobium is partially responsible for the splenomegaly and
hepatomegaly
found in this malarious area, and that treatment for S. haematobium may cause a significant regression of splenomegaly and
hepatomegaly
in children.
...
PMID:Regression of splenomegaly and hepatomegaly in children treated for Schistosoma haematobium infection. 397 Mar 3