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Table 2 Differences between primary MN and IgG4-MN

From: IgG4-related kidney disease (IgG4-RKD) with membranous nephropathy as its initial manifestation: report of one case and literature review

Item

Primary MN

IgG4-MN

Clinical manifestations

Often without damaging other systems

Other with multi-system injuries including lacrimal gland inflammation, salivary gland inflammation, and pancreatitis

Laboratory tests

Renal function

Often normal

Often abnormal

Serum IgG4

Often not elevated

(Absolute or relative values) often elevated

Serum IgE

Often not elevated

Often elevated

PLA2R

Often positive

Negative

Pathology

Pathological IgG subtypes

Various

Mainly IgG4

Interstitial damage

Without plasma cell infiltration and often without interstitial damage

With plasma cell infiltration and often with interstitial damage

Treatment protocol

Hormone dosage

Typically adequate (Prednisone dose that was 1–2 mg/kg/d)

Generally medium and small dose (Prednisone dose that induced was 30–40 mg/d)

Withdrawal of hormone

Hormone are withdrawn regularly, and will be stopped when the condition is alleviated

Maintenance is required