UPJ Obstruction in Children in Lebanon — انسداد الوصل الحالبي الحويضي

انسداد الوصل الحالبي الحويضي عند الأطفال في لبنان · Syndrome de Jonction Pyélo-Urétérale chez l'Enfant au Liban

Expert UPJ obstruction treatment in children in Lebanon by Dr. Anthony Kallas Chemaly — fellowship-trained pediatric urologist. Fellowship-trained at Robert-Debré (Paris). Serving Achrafieh, Verdun, Hamra, Jounieh, and all of Beirut and Mount Lebanon.

Dr. Anthony Kallas Chemaly

Pediatric Urologist · Fellowship-trained in Europe

  • 📍 HDF (Achrafieh) · CMC (Clemenceau) · MLH (Hazmieh)
  • 📞 Clinic: +961 1 398 630
  • WhatsApp: +961 3 551 326
  • 🌐 Arabic · French · English

Medically reviewed by: Dr. Anthony Kallas Chemaly

Last reviewed: April 5, 2026

Sources used on this page: trusted clinical references and pediatric-hospital resources listed below.

What Is UPJ Obstruction?

Ureteropelvic junction (UPJ) obstruction is a condition where the flow of urine is blocked or restricted at the point where the renal pelvis (the funnel-shaped part of the kidney that collects urine) connects to the ureter (the tube that carries urine to the bladder). It is the most common cause of significant hydronephrosis (swelling of the kidney) in children. The obstruction can be caused by an intrinsic narrowing of the ureter, a kink, or an abnormal blood vessel (crossing vessel) that compresses the junction. UPJ obstruction is frequently detected before birth during routine prenatal ultrasound, making it one of the most commonly diagnosed urological conditions in infants.

Signs, Symptoms, and Prenatal Detection

Most cases of UPJ obstruction are detected prenatally when a routine ultrasound shows dilation of the kidney (hydronephrosis) in the fetus. After birth, many infants have no symptoms and the condition is confirmed with postnatal ultrasound. In older children or those not diagnosed prenatally, symptoms may include flank or abdominal pain (especially after drinking large amounts of fluid), urinary tract infections, blood in the urine, or a palpable abdominal mass in newborns. Some children experience intermittent pain that corresponds to episodes of impaired drainage.

Diagnosis: Imaging and Functional Studies

After the initial ultrasound confirms hydronephrosis, further evaluation is needed to determine the severity of the obstruction and its impact on kidney function. The MAG3 diuretic renogram is the gold-standard functional study — it uses a small amount of radioactive tracer to measure how well each kidney drains and what percentage of overall kidney function each side contributes. A voiding cystourethrogram (VCUG) may also be performed to rule out vesicoureteral reflux as a contributing factor. Together, these tests allow the pediatric urologist to distinguish between obstruction that requires surgery and hydronephrosis that can be safely observed.

Observation vs. Surgery: When Is Intervention Needed?

Not every child with UPJ obstruction needs surgery. Mild to moderate hydronephrosis with preserved kidney function is often monitored with serial ultrasounds and repeat renograms. Many of these cases improve or stabilize on their own, particularly when detected prenatally. Surgery is recommended when there is worsening hydronephrosis, a decline in differential kidney function (typically below 40%), recurrent urinary tract infections, or significant pain. The decision is based on objective data — not a single test, but the trend over time.

Pyeloplasty: The Standard Surgical Treatment

When surgery is indicated, pyeloplasty is the procedure of choice. The surgeon removes the narrowed or obstructed segment of the UPJ and reconstructs the connection between the renal pelvis and the ureter, creating a wide, unobstructed drainage pathway. The Anderson-Hynes dismembered pyeloplasty is the most commonly performed technique and has a success rate exceeding 95%. Pyeloplasty can be performed through a small flank incision (open approach) or laparoscopically, depending on the child's age, size, and anatomy. A temporary ureteral stent or nephrostomy tube may be placed to support healing and is typically removed within a few weeks.

Dr. Kallas Chemaly's Approach to UPJ Obstruction

Dr. Kallas Chemaly trained in pyeloplasty — both open and laparoscopic — at leading European pediatric surgery centers including Robert-Debré (Paris), Queen Fabiola Children's Hospital (Brussels), and HFME (Lyon). He takes a data-driven approach: each child undergoes thorough imaging and functional assessment before any treatment decision is made. For cases that require surgery, he selects the approach best suited to the child's anatomy and age. He explains each step to parents in their preferred language (Arabic, French, or English) and provides close postoperative follow-up to ensure optimal outcomes. His goal is straightforward — protect the kidney, relieve the obstruction, and minimize the burden on the child and family.

References

Serving families across Beirut and Mount Lebanon

Dr. Kallas Chemaly treats UPJ obstruction in children from Achrafieh, Gemmayzeh, Saifi, Sodeco, Verdun, Hamra, Clemenceau, Ras Beirut, Rabieh, Mtayleb, Brummana, Beit Mery, Bikfaya, Mansourieh, Kornet Chehwan, Antelias, Dbayeh, Jounieh, Kaslik, Hazmieh, Yarze, and across Keserwan, Metn, and Baabda.

Related Conditions

HydronephrosisKidney StonesPosterior Urethral Valves

Frequently Asked Questions

No. Many cases of UPJ obstruction detected prenatally or in infancy are mild and resolve on their own with time. These children are monitored with regular ultrasounds and, if needed, a MAG3 diuretic renogram to track kidney function. Surgery (pyeloplasty) is recommended when the obstruction is causing worsening hydronephrosis, decreased kidney function, recurrent infections, or pain. A pediatric urologist will determine whether your child needs observation or intervention.
Pyeloplasty is the standard surgical procedure to correct UPJ obstruction. The surgeon removes the narrowed or obstructed segment where the renal pelvis meets the ureter and reconnects them to create a wide, unobstructed drainage pathway. Pyeloplasty has a success rate exceeding 95% and can be performed through an open incision or laparoscopically depending on the child's age and anatomy. It is typically a one-time procedure with excellent long-term outcomes.
Most children spend 1 to 2 nights in the hospital after pyeloplasty. A temporary ureteral stent or drainage tube may be placed during surgery and removed within a few weeks. Children typically return to normal activities within 2 to 4 weeks, though strenuous physical activity is restricted for about 6 weeks. Follow-up ultrasounds are performed at regular intervals to confirm that the kidney is draining well and the repair is holding.

Concerned about your child?

Early evaluation leads to better outcomes. Book a consultation with Dr. Kallas Chemaly today.