Persistent Lymphadenopathy due to IgG4-Related Disease

<div class="floats-full-page floats-full-page-figure"><h2>Figure 3</h2><div class="floats-full-page-caption"><table>IgG (a) and IgG4 (b) stains, 4x magnification.  These stains show an IgG4+/IgG+ cell ratio estimated at 30% (black arrow head: IgG staining, solid black arrow = IgG4 staining).</table></div><div class="floats-full-page-content"><table class="table-group" width="800px"><tr class="fig-image" id="a"><td><img alt="158208.fig.003a" src="https://static-01.hindawi.com/articles/crii/volume-2012/158208/figures/158208.fig.003a.jpg" /></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(a) </b></td></tr></table></td></tr><tr class="fig-image" id="b"><td><img alt="158208.fig.003b" src="https://static-01.hindawi.com/articles/crii/volume-2012/158208/figures/158208.fig.003b.jpg" /></td></tr><tr class="fig-caption"><td align="center"><table><tr><td><b>(b) </b></td></tr></table></td></tr></table></div></div>

Figure 3 | Persistent Lymphadenopathy due to IgG4-Related Disease

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Figure 3: Persistent Lymphadenopathy due to IgG4-Related Disease

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Figure 3

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