Bilateral Hydronephrosis with Recurrent Infections

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Headache and a syndrome of bilateral hydronephrosis.

A 33-year-old woman presented in January 1980 with symptoms of persisting severe pain in the lower abdomen and weight loss. During menstruation there was worsening of the pain, nausea and vomiting. She had periods of headache, which impressed as a vascular headache. Seven years previously she consulted an internist because of general malaise. He found no cause; however the erythrocyte sedimenta...

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Abdominoscrotal hydrocele with bilateral hydronephrosis in an adult: case report.

Abdominoscrotal hydrocele is a rare entity with unclear etiology which may be diagnosed with general examination and ultrasound imaging. During examination it may misinterpreted as acute urinary retention of the bladder (globe-like) especially if associated with hydronephrosis. It should be treated surgically. Here we present a case of left abdominoscrotal hydrocele with accompanying left grade...

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Bilateral Hydronephrosis and Cystitis Resulting from

Ketamine associated urinary dysfunction has become increasingly more common worldwide. Point-of-care ultrasound (POCUS) is an established modality for diagnosing hydronephrosis in the emergency department. We describe a case of a young male ketamine abuser with severe urinary urgency and frequency in which POCUS performed by the emergency physician demonstrated bilateral hydronephrosis and a fo...

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Bilateral hydronephrosis caused by vaginal prolapse.

INTRODUCTION Even though it is uncommon, uterine prolapse can cause compression of ureters and bilateral hydronephrosis, predisposing to arterial hypertension and renal failure. Hydronephrosis consequent to cystocele and to vaginal prolapse is even rarer. CASE REPORT This paper reports on a 59 year-old patient, Caucasian, obese and hysterectomized who presented complete vaginal prolapse with ...

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recurrent infections and bilateral uveitis in a patient cd8 deficiency

cd8 deficiency is a rare primary immunodeficiency with low or absent peripheral cd8 cells which results from tap deficiency, zap 70 deficiency and cd8 α gene mutation. we report a 14 year old female who presented with a history of recurrent pneumonia, bronchiectasis, otitis, severe varicella, herpetic lesions of mouth, bilateral uveitis, and cataract formation since the age of 8 years. she had ...

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ژورنال

عنوان ژورنال: Paediatrica Indonesiana

سال: 2017

ISSN: 2338-476X,0030-9311

DOI: 10.14238/pi19.3-4.1979.111-6