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1.
Tunis Med ; 85(2): 150-4, 2007 Feb.
Article in French | MEDLINE | ID: mdl-17665664

ABSTRACT

BACKGROUND: Schistosomia haematobium infection has been eradicated from Tunisia since 1980. Only some imported cases are noted each year. AIM: The authors report nine cases of Schistosomia haematobium infection diagnosed. METHODS: The diagnosis was carried out within the framework of a survey carried out by the service of Pediatry of the hospital Mongi Slim of Tunis concerning 20 students of African extraction. RESULTS: Hematuria was found in all cases. Schistosomia haematobium infection is diagnosed in all patients by urinary parasitologic examination. Radiological evaluation had revealed mild uroradiologic abnormalities in five patients. All patients were treated by praziquantel. Remission was confirmed by urinary sterilization. Radiologic abnormilities persisted in 3 patients. CONCLUSION: Radiological evaluation and regular follow-up after treatment of students with Schistosomia haematobium infection is required.


Subject(s)
Schistosomiasis haematobia/diagnosis , Adolescent , Adult , Anthelmintics/therapeutic use , Child , Hematuria/parasitology , Humans , Male , Praziquantel/therapeutic use , Schistosomiasis haematobia/drug therapy
2.
Arch Pediatr ; 12(7): 1120-3, 2005 Jul.
Article in French | MEDLINE | ID: mdl-15964528

ABSTRACT

UNLABELLED: Cushing's syndrome reveals McCune-Albright syndrome in a minority of patients. Bilateral adrenalectomy is performed on the majority of cases. CASE REPORT: We present a case of McCune-Albright syndrome revealed by a Cushing's syndrome treated by metyrapone. Results were good, after a 4-year follow up. CONCLUSION: Treatment with metyrapone could be recommended, for some patients, in McCune-Albright syndrome with Cushing's syndrome before chirurgical treatment.


Subject(s)
Cushing Syndrome/drug therapy , Enzyme Inhibitors/therapeutic use , Fibrous Dysplasia, Polyostotic/drug therapy , Metyrapone/therapeutic use , Adrenal Hyperplasia, Congenital/complications , Adrenal Hyperplasia, Congenital/drug therapy , Cushing Syndrome/complications , Female , Fibrous Dysplasia, Polyostotic/complications , Humans , Infant , Treatment Outcome
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