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1.
Article in English | MEDLINE | ID: mdl-29283062

ABSTRACT

INTRODUCTION: Patients with severe thrombocytopenia are presumed to be at increased risk for bleeding, and consequently it has been a standard practice for the past four decades to give allogeneic platelet transfusions to severely thrombocytopenic patients as supportive care. Platelet transfusions may be given either prophylactically to reduce the risk of bleeding, in the absence of clinical hemorrhage (prophylactic transfusions), or to control active bleeding when present (therapeutic transfusions). CONCLUSION: Here we review the structure and function of platelets and discuss the mechanisms of alloimmunization to platelet transfusion.


Subject(s)
Blood Platelets/physiology , Blood Platelets/ultrastructure , Platelet Transfusion , Thrombocytopenia/therapy , Hemorrhage/therapy , Humans , Thrombocytopenia/blood
2.
Lett Drug Des Discov ; 14(2): 135-138, 2017.
Article in English | MEDLINE | ID: mdl-28018158

ABSTRACT

Urogenital schistosomiasis is a chronic infection caused by the human blood fluke Schistosoma haematobium. Schistosomiasis haematobium is a known risk factor for cancer leading to squamous cell carcinoma of the urinary bladder (SCC). This is a neglected tropical disease endemic in many countries of Africa and the Middle East. Schistosome eggs produce catechol-estrogens. These molecules are metabolized to active quinones that cause alterations in DNA (leading in other contexts to breast or thyroid cancer). Our group have shown that schistosome egg associated catechol estrogens induce tumor-like phenotypes in urothelial cells, originated from parasite estrogen-host cell chromosomal DNA adducts and mutations. Here we review recent findings on the role of estrogen-DNA adducts and how their shedding in urine may be prognostic of schistosome infection and/or represent potential biomarkers for urogenital schistosomiasis associated bladder cancer and infertility.

3.
Z Gastroenterol ; 54(7): 653-60, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27429103

ABSTRACT

In 2000, the World Health Organization (WHO) issued an ultrasound field protocol for assessing the morbidity due to Schistosoma (S.) haematobium and S. mansoni. The experience with this classification has recently been reviewed systematically. The WHO protocol was well accepted worldwide. Here we review the use of ultrasound to assess the morbidity due to schistosomiasis with emphasis on easy, quick, and reproducible ways that can be used in the field. Findings obtained with high-end ultrasound scanners in the hospital setting that might eventually have applications in the field are also described.


Subject(s)
Diagnostic Errors/prevention & control , Image Enhancement/methods , Schistosomiasis/diagnostic imaging , Ultrasonography/methods , Diagnosis, Differential , Evidence-Based Medicine , Humans
4.
Exp Parasitol ; 122(3): 250-3, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19361503

ABSTRACT

Estradiol is a steroid hormone secreted principally by the ovarian follicles in vertebrate animals. We have identified the production of an estradiol-related molecule in the trematodes Schistosoma haematobium and Schistosomiasis mansoni. We show in this work that this molecule related to estradiol is present in schistosome worm extracts. The detection method ELISA specific for estradiol, revealed the expression of this estradiol-related molecule in schistosome worm extracts, but not in Fasciola hepatica worm extracts. Our results demonstrate for the first time the production of an estradiol-related compound by a human parasite of the genus Schistosoma.


Subject(s)
Antigens, Helminth/biosynthesis , Estradiol/biosynthesis , Schistosoma haematobium/metabolism , Schistosoma mansoni/metabolism , Adolescent , Adult , Animals , Antigens, Helminth/analysis , Cattle , Child , Child, Preschool , Cricetinae , Enzyme-Linked Immunosorbent Assay , Estradiol/analysis , Estradiol/immunology , Fasciola hepatica/immunology , Fasciola hepatica/metabolism , Female , Humans , Luteinizing Hormone/blood , Male , Mesocricetus , Mice , Mice, Inbred BALB C , Schistosoma haematobium/immunology , Schistosoma mansoni/immunology , Schistosomiasis haematobia/metabolism , Schistosomiasis haematobia/parasitology , Schistosomiasis mansoni/metabolism , Schistosomiasis mansoni/parasitology , Testosterone/blood , Young Adult
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