Diagnostic Dilemma

Hypoalbuminemia with hypertension


Author:
Question

A 6-year-old male child born of second-degree consanguineous marriage presented with generalized edema gradually increasing since 6 months. Edema first started with ascitis and then involved the rest of the body. He had been treated with Furosemide intermittently. His young brother also had similar complaints but was now all right. On examination he had anasarca and blood pressure was 140/100 mm of Hg. Other examination findings were normal. His investigations revealed:
· Urine Albumin: 1+
· 24 hours urine albumin = 126 mg/24 hours.
· Serum total proteins = 4.2 gm/dl.
· Serum albumin = 1.7 gm/dl
· S. SGOT = 72 IU/L
· S. SGPT = 97 IU/L
· BUN, Creatinine, Cholesterol, S. electrolytes – Normal
· USG Abdomen – Mild hepatomegaly with increased echogenicity of both kidneys. Color Doppler was normal.
· Ascitic tap = 99 cells (30% polymorphs, 70% lymphocytes) with proteins = 0.45 gm%.
· HIV, HBsAg, ANA, dsDNA, S. Ceruloplasmin, 24 hours urinary copper = Normal.

He was treated with Furosemide, Spironolactone, Nifedipine, IV antibiotics to which he responded.

His repeat LFT after 14 days showed improvement:
· Serum total proteins = 4.9 gm/dl.
· Serum albumin = 2.3 gm/dl
· S. SGOT = 69 IU/L.
· S. SGPT = 50 IU/L.
· Technetium liver scan showed normal liver.

A liver biopsy could not be done due to ascitis. Thus this child has unexplained ascitis with generalized edema, hypoalbuminemia, hypertension and marginally dysfunctional liver functions and normal renal function tests.



What is the cause of hypertension and hypoalbuminemia in this child?
Expert Opinion :
The authors have replied that vitamin B12 levels were normal in this child and so it was not infantile tremor syndrome and there was no response to Inj B12. The VMA did not show neuroblastoma
Answer Discussion :
G
ghussai
bubble
The single pathology that can expalin the whole picture is nonrenal systemic hypertension causing chronic congestive heart failure and the secondary venous congestion is causing some hepatic dysfunction and protein losing enteropathy.Otherwise, there must be two pathological processes since the renal function{including 24 hr urinary protein} is essentially normal.
With regard to the systemic hypertension,is there any diffrence between the UL and LL?.
Withregard to the hypoalbuminuria and mild liver disfunction,along with this ansacra,I will think of constrictive pericarditis{?TB}.Another possibility is that this kid might have inestinal lymphagectasis.
In both states,check the stool for protein losing enteropathy i.e. alpha 1antitrypsin

20 years ago
M
mohamed zaki
bubble
polycystic diease of liver and kidney
20 years ago

View More Comments

Disclaimer: The information given by www.pediatriconcall.com is provided by medical and paramedical & Health providers voluntarily for display & is meant only for informational purpose. The site does not guarantee the accuracy or authenticity of the information. Use of any information is solely at the user's own risk. The appearance of advertisement or product information in the various section in the website does not constitute an endorsement or approval by Pediatric Oncall of the quality or value of the said product or of claims made by its manufacturer.
0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0