hematuria/vomă

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[Cough, vomiting, diarrhea, fever, convulsions, hematuria, death].

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Recurrent hematuria: a novel clinical presentation of hereditary complete complement C4 deficiency.

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A 10-year-old boy suffered from recurrent attacks of fever, vomiting, and hematuria. During disease flares, circulating immune complexes were detected in the serum. Elevated levels of Bb, Ba, and C3a indicated complement activation through the alternative pathway. Complement C4 was undetectable. C4

Efficacy of Palliative Bladder Radiotherapy for Hematuria in Advanced Bladder Cancer Using Contemporary Radiotherapy Techniques.

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The aim of this study was to review the outcomes of palliative radiotherapy (RT) for hematuria treated with modern RT techniques.This was a retrospective cohort study. The primary endpoint was symptom response rate. Secondary endpoints included symptom

An unusual case of hematuria in a young female: renal artery embolism, mitral stenosis, and sinus rhythm.

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Renal artery embolism (RAE) is an uncommon entity that is most often secondary to a cardiac source. Most reported cases have been in patients with underlying atrial fibrillation (AF), and occurrence of RAE, especially in patients with valvular heart disease, and sinus rhythm is very rare. We

Hematuria as an adverse outcome following provocative growth hormone stimulation testing in children.

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BACKGROUND Provocative growth hormone (GH) stimulation testing is used to evaluate short stature and growth failure in children. Agents commonly used for testing include clonidine, arginine and glucagon. While stimulation testing is generally considered safe, gross hematuria has been described as a

Flank pain and hematuria is not always a kidney stone

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Patients with flank pain and hematuria are common emergency department presentations of nephrolithiasis. We may anchor on this etiology and potentially miss other less common differentials. We present a case of a patient with hematuria and flank pain typical of nephrolithiasis who was diagnosed with

Focal segmental glomerulosclerosis associated with mitochondrial cytopathy: report of two cases with special emphasis on podocytes.

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We report two children with focal segmental glomerulosclerosis (FSGS) associated with mitochondrial cytopathy (MC). Case 1 was diagnosed as MC with the findings of ptosis, ophthalmoplegia, failure to thrive, high serum lactate and pyruvate levels, ragged red fibers in muscle biopsy and the common

Nonoperative treatment of isolated posttraumatic intraperitoneal bladder rupture in children-is it justified?

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OBJECTIVE Open surgical repair has been the standard treatment for intraperitoneal bladder rupture. We sought to explore the possibility of nonoperative treatment of isolated intraperitoneal bladder rupture in children. METHODS Eight children (4 girls and 4 boys) with a mean age of 6.3 +/- 4.6 years

Renovascular hypertension associated with pseudoaneurysm following blunt trauma.

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We present the case of a 21-year-old man who developed a renal artery pseudoaneurysm following a 7-foot fall onto his back. He initially presented with gross hematuria, left flank pain, and back pain. He was observed in the hospital for 3 days and discharged. One week later, he was readmitted with

Copperhead envenomations: clinical profiles of three different subspecies.

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Copperhead envenomation cases reported in the literature frequently lack identification of the subspecies of copperhead responsible for the envenomation. Whether subspecific identity would be useful in predicting possible different toxicity profiles may have clinical relevance. We report here the

A rare presentation of simple renal cyst: gastrointestinal obstruction.

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Simple renal cysts are one of the most common lesions in elderly. These cysts are usually asymptomatic but when the size of these cysts increase, we would see symptoms such as hypertension, hematuria, flank pain or urinary obstruction. In this study, we explore a case of small bowel obstruction that

[Intermittent hydronephrosis. A clinical study in 23 pediatric patients].

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BACKGROUND It is difficult to diagnose intermittent hydronephrosis and to decide the indication of surgical intervention. We investigated 23 cases of intermittent hydronephrosis. METHODS From 1978 to 1995, a total of 23 patients were diagnosed as intermittent hydronephrosis in our institution. We

[Bilateral angiomyolipomas of the kidney in Bourneville's tuberous sclerosis].

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We report on a 25-year-old patient diagnosed as having Bourneville tuberous sclerosis with a giant angiomyolipoma 16 X 12 cm. in diameter, and two small angiomyolipomas in the left kidney, multiple asymptomatic angiomas in the right kidney and two 1 cm. diameter angiomas in the liver. The presenting

A case report of undiagnosed postpartum hemolytic uremic syndrome.

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BACKGROUND Postpartum hemolytic uremic syndrome (PHUS) is a severe thrombotic microangiopathy (TMA) that is clinically characterized by hemolytic anemia, renal dysfunction, and low platelet levels after childbirth. Here, we report a rare case of unexpected death due to PHUS. METHODS A 23-year-old

Aorta-left renal vein fistula in a woman.

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Spontaneous rupture of an abdominal aortic aneurysm into a retroaortic left renal vein is an uncommon occurrence. A 55-year-old woman presented with shortness of breath, vomiting, and diffuse abdominal pain that had radiated to her back and legs for the preceding 10 days. A pulsatile abdominal mass,

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