Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Polyarteritis nodosa

Polyarteritis nodosa (PAN) is a rare, clinically heterogeneous, rheumatologic disease characterized by necrotizing inflammatory lesions affecting small- and medium-sized blood vessels. PAN most commonly affects skin, joints, peripheral nerves, the gut, and the kidney.

Proteinuria

Increased levels of protein in the urine.

Total: 1

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PMID (PMCID)
28197518 (5297566)	OTHER
	Hepatitis B viremia manifesting as polyarteritis nodosa and secondary membranous nephropathy.
	Balwani MR, Kute VB, Shah PR, Shah M, Shinde SG, Shah J, Trivedi HL. J Nephropharmacol. 2016;5(2):119-121.
	Renal involvement in hepatitis B-polyarteritis nodosa (HBV-PAN) usually occurs in the form of hypertension, microscopic hematuria, proteinuria but nephrotic range proteinuria or renal failure is very uncommon.