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[Treatment of reno-ureteral lithiasis with ESWL in obese patients. Apropos of 150 patients].
Arch Esp Urol
October 2003
Clinique Saint Pierre, Guadaloupe, Francia.
Objectives: Obesity is considered a significant risk factor for diseases such as hypertension, diabetes, coronary artery disease, and metabolic diseases, increasing considerably the risk for surgery. We have treated with ESWL a significant number of patients with the aim of avoiding operations which could be long and have associated complications due to the patient's condition.
Methods: From April 2000 to May 2002 we treated 150 obese patients with kidney and/or ureteral stones using a Nova Ultima lithotripter.
Testicular torsion in adult, is an uncommonly etiology, but we should make differencial diagnosis in every person over thirty years old, with acute scrotum. The wrong diagnosis raises the incidence orchiectomy in adults for vascular etiology. We report a male of 74 years old with acute scrotum and review of the literature.
View Article and Find Full Text PDF[Ureteroplasty using the appendix: apropos of a case].
Arch Esp Urol
June 2002
Servicio de Urología, Hospital Juan Canalejo, La Coruña, España.
Objective: To report a case of ureteroplasty using the vermiform appendix.
Methods: Herein we describe a patient who underwent partial resection of the ureter due to a neoplasm. The ureteral defect was repaired using the vermiform appendix.
[Pathological pelvic kidney. Apropos of 11 cases].
Ann Urol (Paris)
July 2002
Clinique urologique A, CHU Ibn Sina, Rabat, Maroc.
The diseases ectopic kidney is a rare malformation. It can be associated with other urological or nonurological malformation. We report 11 cases observed between 1980 and 1998.
View Article and Find Full Text PDF[Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
Encephale
June 2001
Service de Psychopathologie de l'Enfant et de l'Adolescent, CHU Pitié-Salpêtrière, 47, boulevard de l'Hôpital, 75013 Paris.
Deletion of chromosome 22q11 concerns nearly 1/5.000 births, and is the most frequent interstitial microdeletion. The deletion generates various phenotypes which were initially regarded as distinct syndromes.
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