Wednesday, February 11, 2009
Loin Pain-Hematuria Syndrome
The loin pain-hematuria syndrome occurs when glomerular hematuria occurs in conjunction with renal colic, in the absence of glomerulonephritis or a worsening of renal function. It is not a common disorder, though appears to be more common in women than in men. It appears to lie along the same continuum as thin basement membrane disease, as a substantial number of patients with loin pain-hematuria syndrome who undergo biopsy demonstrate irregularities (either too thick or too thin) in the glomerular basement membrane; in thin basement membrane disease, however, there does not seem to be a predilection for females and hematuria is typically painless. Approximately 20% of patients with suspected loin pain-hematuria syndrome who undergo biopsy are subsequently found to have IgA deposits--thus biopsy is warranted if the diagnosis of loin-pain hematuria syndrome is suspected. The pathophysiology of loin pain-hematuria syndrome is postulated to be based on irregular basement membranes, which will occasionally rupture and result in glomerular bleeding. When the bleeding is significant enough, it could conceivably result in swelling of the renal capsule and resultant pain. A decent review can be found in this 2006 KI article.
Labels:
glomerular disease,
Nathan Hellman,
urinalysis
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3 comments:
I blogged about this article.
http://xrl.in/1kre
I just want to get straight to the point. My mum is suffering from Thin basement membrane disease. She has been for over a year now and she doesnt seem to be getting any better Shes getting worse. Ive tried reseraching about this disease but its all the same thing.. Shes done renal biopsy and has been getting enjections for the last year 3 times a week.. What is their to do? Doctors wont tell us what are the options. So can someone help me please. Its a very scary moment for us and we dont wanna lose her.. So any advice would be appreciated please.
PLEASE VISIT WWW.LIVINGWITHLPHS.CO.UK FOR MORE INFORMATION ON LOIN PAIN HEMATURIA SYNDROME - THIS SITE HAS BEEN SET UP TO HELP RAISE AWARENESS ON THIS CONDITION, TO HAVE ALL INFORMATION ON THE CONDITION IN ONE PLACE AND FINALLY TO HELP AND SUPPORT ALL THOES THAT SUFFER WITH THE CONDITION. PLEASE VISIT FOR MORE INFORMATION ON THE LIVING WITH LPHS SUPPORT GROUP ON FACEBOOK. THANKS
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