Unconfigured Ad

Collapse

screening for nephroblastoma

Collapse
This topic has been answered.
X
X
 
  • Time
  • Show
Clear All
new posts
  • Admin
    Administrator

    • Sep 2020
    • 6950

    #1

    quiz screening for nephroblastoma

    Children with which of the following conditions should receive screening renal ultrasounds for nephroblastoma (Wilms tumor)?

    A a teenager who had unilateral Wilms’ at four years of age

    B Denys-Drash syndrome

    C end stage renal failure

    D cryptorchidism

    E isolated Wilms’ tumor in a sibling
    Want to support Pediatric Surgery Club and get Donor status?

    click here!
  • Answer selected by Admin at 09-08-2023, 09:38 PM.
    Admin
    Administrator

    • Sep 2020
    • 6950

    Originally posted by Abusnaina mohammed
    B Denys-Drash syndrome
    Correct

    Wilms tumor usually presents as an asymptomatic abdominal mass in an otherwise healthy child. Up to one third of patients will have associated symptoms of abdominal pain, fever, anemia, hematuria or hypertension.

    Current theories of tumor development suggest a genetic mutation that predisposes to the persistence of nephrogenic rests. Nephrogenic rests are also present in the predisposition syndromes of WAGR (Wilms tumor- aniridia - genital anomalies - retardation), Denys-Drash (nephropathy, intersex disorders), Beckwith-Wiedemann (hemihypertrophy, macroglossia, hypoglycemia) and isolated hemihypertrophy. These patients may benefit from screening ultrasound. The frequency of screening is dependent on the syndrome.

    Current recommendations suggest surveillance abdominal ultrasound examinations for the above patients, siblings of patients with familial Wilms and offspring of patients with bilateral Wilms.

    Patients who have finished therapy for Wilms should have ultrasound examinations every three months until the age of seven years.

    Comment

    • Abusnaina mohammed
      Senior Member
      • Oct 2020
      • 100

      #2
      B Denys-Drash syndrome

      Comment

      • Admin
        Administrator

        • Sep 2020
        • 6950

        #3
        Originally posted by Abusnaina mohammed
        B Denys-Drash syndrome
        Correct

        Wilms tumor usually presents as an asymptomatic abdominal mass in an otherwise healthy child. Up to one third of patients will have associated symptoms of abdominal pain, fever, anemia, hematuria or hypertension.

        Current theories of tumor development suggest a genetic mutation that predisposes to the persistence of nephrogenic rests. Nephrogenic rests are also present in the predisposition syndromes of WAGR (Wilms tumor- aniridia - genital anomalies - retardation), Denys-Drash (nephropathy, intersex disorders), Beckwith-Wiedemann (hemihypertrophy, macroglossia, hypoglycemia) and isolated hemihypertrophy. These patients may benefit from screening ultrasound. The frequency of screening is dependent on the syndrome.

        Current recommendations suggest surveillance abdominal ultrasound examinations for the above patients, siblings of patients with familial Wilms and offspring of patients with bilateral Wilms.

        Patients who have finished therapy for Wilms should have ultrasound examinations every three months until the age of seven years.
        Want to support Pediatric Surgery Club and get Donor status?

        click here!

        Comment

        • Titolugo
          True Member

          • Nov 2020
          • 9

          #4
          B

          Comment

          Working...