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Cap polyposis and colitis cystica profunda: a rare association

Authors :
Riad Arana
Yann Parc
Nizar El-Murr
Magali Svrcek
Jacques Cosnes
Jean-François Fléjou
Service d'anatomie et cytologie pathologiques [CHU Saint-Antoine]
Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Saint-Antoine [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)
Université Pierre et Marie Curie - Paris 6 (UPMC)
CHU Saint-Antoine [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Source :
Histopathology, Histopathology, Wiley, 2013, 64 (4), pp.604-607. ⟨10.1111/his.12292⟩, Histopathology, 2013, 64 (4), pp.604-607. ⟨10.1111/his.12292⟩
Publication Year :
2013
Publisher :
HAL CCSD, 2013.

Abstract

International audience; : Cap polyposis and colitis cystica profunda (CCP) are two rare, benign and distinct colorectal conditions whose etiology remains unclear. A rare association between cap polyposis and CCP has already been described. In those cases, cystic glands were present in the submucosal layer of the cap polyps.(1,2) Interestingly, in the present case, lesions of CCP were not intermingled with cap polyps, but were distant from them. This article is protected by copyright. All rights reserved.

Details

Language :
English
ISSN :
03090167 and 13652559
Database :
OpenAIRE
Journal :
Histopathology, Histopathology, Wiley, 2013, 64 (4), pp.604-607. ⟨10.1111/his.12292⟩, Histopathology, 2013, 64 (4), pp.604-607. ⟨10.1111/his.12292⟩
Accession number :
edsair.doi.dedup.....5181edadf6dcdaf5fbfdbaeda8086cf2
Full Text :
https://doi.org/10.1111/his.12292⟩