A CASE STUDY ON PAUCI IMMUNE GLOMERULONEPHRITIS
Ganeshakumara M., K. Bhavani, Praveenkumar K., H. P. Sahana, Jahnavi G. and Dr. Nagarjuna D.*
.
Abstract
Rapidly progressive glomerulonephritis (RPGN) is a syndrome
signified by a precipitous loss of renal function, with features of
glomerulonephritis including dysmorphic erythrocyturia and
glomerular proteinuria. The immune system and the kidneys are
closely linked, and chronic kidney disease (CKD) often results from
various auto(immune) disorders. This is a case report of Pauci immune
glomerulonephritis also called as RPGN (rapidly progressive
glomerulonephritis) of which 35 year female patient was admitted in
hospital with illness of fever and cough, her past medical history
conveys that she is not a known case of hypertension and diabetes
mellitus and she doesn’t have any habits. On physical examination her
BP was found to be 110/70 mm of hg and pulse rate was 90 beats per
minute. On systemic examination diagnosis done with RFT, CBC, Direct
immunofluorescence And Histopathology Report, Vasculitis Profile. based on these reports
the diagnosis is confirmed as Pauci immune glomerulonephritis and vasculitis associated with
ANCA. Treatment is started by giving anticancer drug like Endoxan, methyl prednisolone,
IFA, Folvite and Sodium bicarbonate and supplements. Physician followed the guidelines for
the treatment of pauci immune glomerulonephritis, prescribing anticancer drug can helps to
prevent the active crescent’s with mitotic activity, and prescribing the corticosteroids and
immune suppressants can helps to treat the inflammation and over activity of immune system
can helps to reduce the patient severity. To increase the life expectancy of patient by giving
suitable treatment and advising to maintain self hygiene and Diet.
Keywords: Pauci immune glomerulonephritis, Rapidly progressive glomerulonephritis, Vasculitis associated with ANCA (Anti neutrophil cytoplasmic antibody), Chronic kidney disease (CKD).
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