Divertículo calicial y su diagnóstico incidental / Calyceal diverticulum and its incidental diagnosis

Introducción: El divérticulo calicial se detecta en 0,21 a 0.60 por ciento de los urogramas excretores. Objetivos: Describir una paciente con diagnóstico incidental de esta anomalía y su seguimiento durante 11 años. Presentación del caso: Durante la realización de un urograma excretor para el estudio de una hidronefrosis en una niña de siete años de edad, se detectó un divertículo calicial en el riñón contralateral y después de 11 años de seguimiento ultrasonográfico no se ha demostrado modificación ni complicación del divertículo. Conclusiones: El divertículo calicial es una anomalía congénita que puede mantenerse sin complicaciones durante años por lo que debe tratarse conservadoramente(AU)

ABSTRACT Introduction: Calyceal diverticulum is detected in 0,21 percent to 0.60 percent of excretory urogram. Objectives: To describe a patient with an incidental diagnosis of this anomaly and her follow up during 11 years. Case presentation: During the performance of an excretory urogram for studying a hydronefrosis in a seven years old girl, a calyceal diverticulum was detected in the contralateral kidney; and after 11 years of ultrasonographic follow-up there has been no modifications or complication related with the diverticulum. Conclusions: Calycial diverticulum is a congenital anomaly that can last years without presenting complications. That is why it must be treated conservatively(AU)

[Congenital megacalycosis in a girl with unilateral renal agenesis]. / Wrodzone kielichonercze u dziewczynki z jednostronna agenezja nerki.

Renal agenesis occurs in pediatric population with the incidence 1:500- 2000 children. It is more often diagnosed in boys and on the left side of the body. Renal agenesis may be isolated or it may be a part of complex malformation syndrome. Megacalycosis is a very rare anomaly of urinary tract associated with abnormal structure of the kidney pyramids. AIM: The aim of the study was to present for the first time in the medical literature the case of a girl with unilateral renal agenesis and megacalycosis. CASE REPORT: A girl, born at term in good general medical condition, and with normal birth weight was admitted to the hospital because of urinary tract infection caused by E.coli. Antenatal abdominal ultrasounds were normal. In a diagnostic, repeated ultrasound studies, unilateral, left renal agenesis and the righ-sided megacalycosis were found. The right kidney had dilated collecting system, with normal size of renal pelvis and enlarged calyces up to 26 mm. The kidney function was normal. Voiding cystourethrography excluded vesicoureteral reflux. Dynamic scintigraphy 99mTc-EC showed the lack of function of the left kidney, postinflammatory changes and dilation of collecting system without signs of obstruction. During two-years follow up we didn't observe clinical relapse of urinary tract infection. Blood pressure and kidney function were normal. CONCLUSIONS: Complex congenital anomalies of the kidney and the urinary tract (CAKUT) can be diagnosed at any age. Normal antenatal abdominal ultrasound does not exclude CAKUT. Every patient with congenital abnormalities of the kidney and the urinary tract requires long-term follow up, because of increased risk of chronic kidney disease.

Horseshoe kidney with extrarenal calyces and malformed renal vessels

The horseshoe kidney is a congenital fusion anomaly where both kidneys are fused at the lower poles. We report a case of horseshoe kidney in a 70 year-old Thai cadaver. This horseshoe kidney was associated with malformations of renal hila, sinuses, calyces and supernumerary arterial supplies from the dorsal part of the kidney. To our knowledge, the arterial supply to the horseshoe kidney from the dorsal aspect has never been reported. Dissection revealed six aberrant renal arteries directly originated from the abdominal aorta supplying directly the renal segments. We believe that it was probably due to the persistence of mesonephric arteries. Also, the ascension of the horseshoe kidney in the present case was restricted by one of the renal arteries, not the inferior mesenteric artery. The embryology, anatomy, and the clinical significance of the present case are discussed

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Endovascular management of iatrogenic renal arterial lesions and clinical outcomes.

PURPOSE: We aimed to evaluate iatrogenic renal arterial lesions, including pseudoaneurysm, arteriovenous fistula, and arteriocaliceal fistula, their management by endovascular embolization, and the clinical results. METHODS: Fifty-five patients (forty males, fifteen females) with a median age of 40 years (range, 8-85 years), who underwent endovascular embolization of iatrogenic renal arterial lesions between March 2003 and December 2013 were included in this retrospective study. Types of iatrogenic lesions and details of embolization procedures were reported. Estimated glomerular filtration rate (eGFR), renal function tests, hemoglobin, and hematocrit levels before and after embolization were recorded and compared. RESULTS: Median follow-up was 24 months. We identified 53 pseudoaneurysms, 30 arteriovenous fistulas, and 11 arteriocaliceal fistulas in 55 patients, after percutaneous nephrolithotomy (n=26), renal biopsy (n=21), nephrostomy (n=3), renal surgery (n=3), and extracorporeal shock wave lithotripsy (n=2). Median number of pseudoaneurysms was 1 (range, 1-4) with a median size of 7 mm (range, 1.5-35 mm). Fifty-one patients underwent coil embolization. Median number of coils was 5 (range, 2-21) and median renal parenchymal loss was 5% (range, 1%-50%). There were no significant differences between pre- and postoperative eGFR and serum parameters. CONCLUSION: Iatrogenic renal arterial lesion can be a life threatening condition. Superselective coil embolization is a safe, minimally invasive treatment option with minimal renal parenchymal loss and without significant change in renal function.

Extrarenal calyces: a rare renal congenital anomaly.

The congenital anomalies of urogenital system are not uncommon. The anomalies of renal collecting system form a complex subset of urogenital anomalies. Among these, extrarenal calyces are one of the infrequently found anomalies of the renal collecting system. Extrarenal calyces may be detected incidentally or when thoroughly investigated for its associated complications. We report two cases of extrarenal calyces characterized by the presence of major calyces and renal pelvis outside the renal parenchyma. The awareness of this anomaly can help in making the definitive preoperative diagnosis and prevent injury to pelvicalyceal system during surgery.

Doble sistema pielocalicial completo bilateral / Complete bilateral pelvicalyceal system duplication

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[Partial laparoscopic nephrectomy: treatment for hydrocalicosis due to infundibular stenosis]. / Nefrectomía parcial laparoscópica: tratamiento de hidrocalicosis por estenosis infundibular.

BACKGROUND: This report describes a partial nephrectomy with a minimally invasive approach, carried out laparoscopically as a treatment for a hydrocalicosis caused by a congenital infundibular stenosis. CLINICAL CASE: The patient presented a clinical background of one year of evolution, manifested as recurrent urinary tract infections caused by urine accumulation in the adjacent collecting tubules which were compressed by the superior hydrocalicosis. This procedure was made using a transperitoneal access, making a superior pole resection of the right kidney and respecting the adrenal gland. CONCLUSIONS: In our opinion, to widen the usage of the laparoscopic surgery in urology can benefit patients to reduce post-surgery complications and hospitalization time, with a more comfortable recovery.

Needle renal displacement technique for the percutaneous approach to the superior calix.

We describe a new renal displacement technique using an 18-gauge needle to facilitate superior calix puncture and consequently to decrease intrathoracic morbidity. Initially, a lower or middle calix is punctured with an 18-gauge needle. Then, the proximal end of the needle is progressively pushed in the cephalic direction. Therefore, the kidney is pushed caudally by the lever maneuver. This technique has also been used to immobilize the kidney or to reorient complex and malrotated kidneys.

Caliceal diverticulum in pediatric patients: the spectrum of imaging findings.

BACKGROUND: Caliceal diverticulum (CD) is uncommon in children. As compared to adults, most children with CD are symptomatic. Common complications include stone formation and infection. Correct diagnosis of CD is important for guiding management. OBJECTIVE: To identify imaging findings at diagnosis and follow-up in pediatric patients with CD. MATERIALS AND METHODS: We identified all patients from 2003 to 2010 with a diagnosis of CD. We reviewed presenting symptoms, underlying diseases, complications, management, and all pertinent radiological examinations. RESULTS: Twenty-four patients (2.6 to 18.5 years old, 11 females) had CD. Urinary tract infection was the most common (n = 8) presentation. Diagnosis of CD was based on delayed post-contrast CT in 79% of patients with only one false-negative CT. Most patients (n = 20) had a single CD; others had either 2 CDs (n = 2) or multiple CDs (n = 2). CD diameter ranged from 1.0 to 18.3 cm and grew in five of nine patients who had follow-up studies. Seven patients developed stone in the CD. Fifteen patients (63%) underwent a surgical procedure. CONCLUSIONS: CD is commonly solitary, often grows with time and may mimic other diagnoses, including simple cyst, complex cyst and polycystic kidney disease. Delayed postcontrast CT is highly sensitive in diagnosing CD.

A new operative technique for a rare case of pyelic fusion.

This case report presents the first documented case of pyelic fusion with two sites of obstruction. The patient was diagnosed following antenatal presentation and the operative technique described in this case report is the only way by which the obstructions could be treated with a single procedure. The left pelvicalyceal system was grossly dilated and was draining into the common pelvis via an obstructed calyx in the isthmus of the horse shoe. The common ureter also had a pelviureteric junction stenosis. Incisions were made in the left dilated pelvis and in the obstructed part of the pelviureteric junction and ureter. The two openings were sutured as a culp pyeloplasty using interrupted 6/0 PDS sutures over a 4F JJ stent.

Endoscopic management of completely excluded calices: a single institution experience.

BACKGROUND AND PURPOSE: Excluded calices refer to a single calix or multiple calices that are completely isolated from the collecting system. The etiology is a result of infection, malignancy, or inflammation that is secondary to endoscopic renal surgery. We report our experience with the endoscopic management of excluded calices. PATIENTS AND METHODS: We retrospectively reviewed the data for our patients with a diagnosis of excluded calices. Patients were treated with various endoscopic techniques, all necessitating the formation of a neoinfundibulum. Patients were evaluated for symptomatic and radiographic evidence of resolution. RESULTS: Eight patients were found to have excluded calices. Seven patients had a history of urolithiasis and previous endoscopic renal surgery. One patient had undergone a laparoscopic partial nephrectomy with a postoperative urinary fistula. Six of eight patients were treated with a percutaneous approach followed by laser incision, balloon dilatation, or nephroureteral stent placement. Two objective failures occurred. One patient received re-treatment and has not demonstrated persistence or recurrence since the second procedure. No complications occurred as a result of endoscopic management. CONCLUSION: Excluded calices commonly result from inflammation from previous renal surgery. Goals of management include relief of obstruction, management of stones, and regaining continuity with the remaining collecting system. Successful treatment with endoscopic management involves creation of a neoinfundibulum and placement of a temporary ureteral stent.