Nephrotic Syndrome and Nephritic Syndrome in Children Complete Paediatric Guide
Paediatrics

Nephrotic Syndrome and Nephritic Syndrome in Children Complete Paediatric Guide

[

{

"question": "A 5-year-old boy presents with progressive periorbital swelling for 4 days followed by pedal edema and abdominal distension. Blood pressure is normal. Urinalysis shows 4+ protein with no RBCs. Serum albumin is 1.6 g/dL and cholesterol is elevated. Which mechanism best explains the edema in this child?",

"options": [

"Reduced plasma oncotic pressure leading to fluid shift into interstitial space",

"Increased capillary hydrostatic pressure due to hypertension",

"Primary renal sodium loss",

"Excess erythropoietin production"

],

"correct": 0,

"explanation": "In nephrotic syndrome, massive albumin loss lowers plasma oncotic pressure causing fluid to shift into the interstitial space leading to edema."

},

{

"question": "A 6-year-old child with nephrotic syndrome develops sudden severe abdominal pain, fever, and guarding. Ascitic fluid shows neutrophils and gram positive cocci. Which organism is most commonly responsible?",

"options": [

"Streptococcus pneumoniae",

"Escherichia coli",

"Mycobacterium tuberculosis",

"Pseudomonas aeruginosa"

],

"correct": 0,

"explanation": "Spontaneous bacterial peritonitis in nephrotic syndrome is most commonly caused by Streptococcus pneumoniae due to loss of immunoglobulins."

},

{

"question": "A 7-year-old child develops cola-colored urine, facial edema, and hypertension two weeks after streptococcal pharyngitis. Complement C3 levels are low. What is the most likely diagnosis?",

"options": [

"Minimal change disease",

"Post-streptococcal glomerulonephritis",

"IgA nephropathy",

"Membranous nephropathy"

],

"correct": 1,

"explanation": "Post-streptococcal glomerulonephritis presents with nephritic syndrome 1–3 weeks after streptococcal infection and is associated with low complement levels."

},

{

"question": "A child with nephrotic syndrome develops sudden flank pain and gross hematuria. Doppler ultrasound reveals absence of flow in the renal vein. What is the most likely cause?",

"options": [

"Renal artery stenosis",

"Renal vein thrombosis",

"Ureteric obstruction",

"Acute pyelonephritis"

],

"correct": 1,

"explanation": "Hypercoagulability due to urinary loss of antithrombin III predisposes nephrotic children to renal vein thrombosis."

},

{

"question": "A 4-year-old boy with nephrotic syndrome has persistent heavy proteinuria after 8 weeks of adequate steroid therapy. What is the most appropriate next step?",

"options": [

"Increase steroid dose indefinitely",

"Renal biopsy to evaluate steroid-resistant nephrotic syndrome",

"Stop all treatment",

"Start antibiotics"

],

"correct": 1,

"explanation": "Failure to achieve remission after adequate steroid therapy suggests steroid-resistant nephrotic syndrome requiring renal biopsy."

},

{

"question": "A 10-year-old boy has recurrent episodes of hematuria occurring within 24 hours of upper respiratory infections. Which disease is most likely?",

"options": [

"IgA nephropathy",

"Minimal change disease",

"Membranous nephropathy",

"Post-streptococcal GN"

],

"correct": 0,

"explanation": "IgA nephropathy typically causes recurrent hematuria occurring concurrently with respiratory infections."

},

{

"question": "A child with nephritic syndrome presents with severe headache, vomiting, and seizures. Blood pressure is 180/110 mmHg. What is the most likely cause of neurological symptoms?",

"options": [

"Hypertensive encephalopathy",

"Hypoglycemia",

"Meningitis",

"Septic shock"

],

"correct": 0,

"explanation": "Severe hypertension in nephritic syndrome can cause hypertensive encephalopathy presenting with seizures."

},

{

"question": "A 5-year-old boy with nephrotic syndrome develops tachypnea and sudden pleuritic chest pain. Which life-threatening complication should be suspected first?",

"options": [

"Pulmonary embolism",

"Pleural effusion",

"Bronchial asthma",

"Pneumonia"

],

"correct": 0,

"explanation": "Nephrotic syndrome causes hypercoagulability due to loss of anticoagulant proteins leading to pulmonary embolism."

},

{

"question": "A child with nephritic syndrome has persistent low complement levels for more than 8 weeks. Which diagnosis should be considered?",

"options": [

"Membranoproliferative glomerulonephritis",

"Minimal change disease",

"Focal segmental glomerulosclerosis",

"Diabetic nephropathy"

],

"correct": 0,

"explanation": "Persistent hypocomplementemia beyond 8 weeks suggests MPGN rather than post streptococcal GN."

},

{

"question": "A 6-year-old child with nephrotic syndrome presents with severe edema and respiratory distress. Chest examination reveals decreased breath sounds bilaterally. What is the most likely diagnosis?",

"options": [

"Pleural effusion",

"Pulmonary fibrosis",

"Bronchitis",

"Atelectasis"

],

"correct": 0,

"explanation": "Severe hypoalbuminemia leads to fluid accumulation including pleural effusion."

},

{

"question": "A 7-year-old boy presents with hematuria, proteinuria, and sensorineural hearing loss with a positive family history of kidney disease. What condition is most likely?",

"options": [

"Alport syndrome",

"Minimal change disease",

"IgA nephropathy",

"Post-streptococcal GN"

],

"correct": 0,

"explanation": "Alport syndrome is characterized by hereditary nephritis with hearing loss and progressive renal failure."

},

{

"question": "A child with nephrotic syndrome develops fever and erythema over the leg with tenderness and swelling. What infection is most likely?",

"options": [

"Cellulitis",

"Osteomyelitis",

"Septic arthritis",

"Tuberculosis"

],

"correct": 0,

"explanation": "Children with nephrotic syndrome are prone to bacterial infections including cellulitis due to immune protein loss."

},

{

"question": "A 5-year-old boy presents with massive proteinuria but normal blood pressure and normal complement levels. Electron microscopy would most likely reveal which finding?",

"options": [

"Podocyte foot process effacement",

"Subendothelial immune deposits",

"Mesangial IgA deposition",

"Crescent formation"

],

"correct": 0,

"explanation": "Minimal change disease shows diffuse effacement of podocyte foot processes on electron microscopy."

},

{

"question": "A child with nephritic syndrome presents with oliguria, pulmonary edema, and rising serum creatinine. What is the immediate management priority?",

"options": [

"Fluid restriction and diuretics",

"High protein diet",

"Immediate corticosteroids",

"Insulin infusion"

],

"correct": 0,

"explanation": "Fluid restriction and diuretics are necessary to manage fluid overload and pulmonary edema."

},

{

"question": "A 4-year-old boy with nephrotic syndrome develops frequent relapses whenever steroids are tapered. Which medication is commonly used as a steroid-sparing agent?",

"options": [

"Cyclophosphamide",

"Metformin",

"Atenolol",

"Amoxicillin"

],

"correct": 0,

"explanation": "Cyclophosphamide is used for frequently relapsing or steroid dependent nephrotic syndrome."

}

]

Interactive MCQ Quiz

MCQ Exam Mode

15 Questions
Question 1 of 15

Frequently Asked Questions

Nephrotic syndrome in children is a kidney disorder characterized by heavy protein loss in urine, low blood albumin levels, generalized body swelling, and high cholesterol. It occurs due to damage to the glomerular filtration barrier, most commonly from minimal change disease in paediatric patients.
The main symptoms include periorbital swelling especially in the morning, generalized body edema, frothy urine due to proteinuria, decreased urine output, weight gain from fluid retention, and sometimes abdominal swelling from ascites.
Nephritic syndrome is a kidney condition caused by inflammation of the glomeruli leading to hematuria, hypertension, reduced urine output, mild proteinuria, and edema. It commonly occurs after infections such as post streptococcal glomerulonephritis.
Nephrotic syndrome primarily involves massive proteinuria and severe edema due to damage to the filtration barrier, while nephritic syndrome involves glomerular inflammation leading to hematuria, hypertension, and reduced kidney function.
Minimal change disease is the most common cause of nephrotic syndrome in children, accounting for approximately 80 to 90 percent of paediatric cases.
Common causes include post streptococcal glomerulonephritis, IgA nephropathy, Henoch Schönlein purpura, lupus nephritis, and other immune mediated glomerular diseases.
Diagnosis is based on urine tests showing heavy proteinuria, blood tests showing hypoalbuminemia and hyperlipidemia, and clinical findings such as generalized edema. In some cases renal biopsy may be required.
Diagnosis is made using urinalysis showing hematuria with RBC casts, blood tests revealing reduced complement levels and elevated antistreptococcal antibodies, and clinical features such as hypertension and oliguria.
The first line treatment is corticosteroid therapy, most commonly prednisolone, which helps reduce inflammation and restore normal kidney filtration in minimal change disease.
Major complications include infections such as spontaneous bacterial peritonitis, thromboembolism including renal vein thrombosis, hypovolemia, acute kidney injury, and severe edema.