Anogenital granulomatosis: report of two cases

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F15%3A10290312" target="_blank" >RIV/00216208:11140/15:10290312 - isvavai.cz</a>
Alternative codes found
RIV/00669806:_____/15:10290312
Result on the web
<a href="http://onlinelibrary.wiley.com/doi/10.1111/ced.12490/epdf" target="_blank" >http://onlinelibrary.wiley.com/doi/10.1111/ced.12490/epdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1111/ced.12490" target="_blank" >10.1111/ced.12490</a>

Result language
angličtina
Original language name
Anogenital granulomatosis: report of two cases
Original language description
Anogenital granulomatosis (AGG) is a rare chronic inflammatory disorder of unknown aetiology. It presents clinically with swelling of the genital or anoperineal area, with histopathological findings of noncaseating giant cell granulomas. Some cases of AGG are associated with underlying systemic disease, mainly Crohn disease. We report two patients with AGG. The first was a young man with ulcerative colitiis treated with infliximab, which also alleviated the developing symptoms of AGG. The second was a young woman who was otherwise healthy. After the introduction of complex decongestive therapy, the oedema was considerably reduced in both patients.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FO - Dermatology and venereology
OECD FORD branch
—

Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2015
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Similar results(10)