INTRODUCTION Granulomatous inflammation is a distinctive ...
INTRODUCTION Granulomatous inflammation is a distinctive ...
INTRODUCTION Granulomatous inflammation is a distinctive ...
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Diagnos<strong>is</strong> <strong>is</strong> primarily made by imaging studies. In the case of E. granulosus, CT or MRI scans of<br />
brain typically demonstrate a spherical cystic lesion with smooth borders (Figure 15, 16) (Tuzun<br />
et al., 2002). When the internal images from the protoscolexes "hydatid sand" are seen, the image<br />
can be diagnostic. Midline shift and d<strong>is</strong>tortion of the ventricles are common. Lesions are usually<br />
not inflamed and thus do not have surrounding edema or enhancement. The cyst wall usually<br />
shows a rim of low signal intensity on both TI- and T2-weighted images. T2-weighted images are<br />
better than TI-weighted images in revealing the wall of the hydatid cyst because the low-signalintensity<br />
cystic wall contrasts well with the high-signal-intensity fluid content Cysts may be found<br />
outside the CNS, which suggests that the CNS lesion <strong>is</strong> also due to hydatid d<strong>is</strong>ease (Haliloglu et al.,<br />
1997). The CT appearance of E. multilocular<strong>is</strong> <strong>is</strong> less d<strong>is</strong>tinct. It may present as an ill-defined mass<br />
lesion and most cases will also have evidence of liver involvement (David et al., 2004).<br />
Figure 15. Hydatid. Axial contrast enhanced T1 weighted<br />
image reveals round well-circumscribed hypointense cyst.<br />
NoteMarked shift of midline structures to left. No contrast<br />
enhancement <strong>is</strong> seen. (Meric and Baki, 1998)<br />
Figure 16. Hydatid. Axial contrast enhanced T1<br />
weighted image reveals multiple cerebral cysts.<br />
Note shift of midline structures to left.. (Meric and<br />
Baki, 1998)<br />
In doubtful cases, serologic assays can be diagnostic. Enzyme-linked immunosorbent assay<br />
(ELISA) or indirect hemagglutination assays are readily available and can be confirmed by<br />
immuno blot assays. However, the sensitivity <strong>is</strong> not optimal for extrahepatic d<strong>is</strong>ease. For E.<br />
multilocular<strong>is</strong>, the EM2 ELISA with purified antigen <strong>is</strong> the confirmation test (David et al., 2004).