tailieunhanh - Báo cáo y học: "Rectal mucosal prolapse syndrome as an unusual gastrointestinal manifestation of Sjögren's syndrome: a case report"

Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: TRectal mucosal prolapse syndrome as an unusual gastrointestinal manifestation of Sjögren's syndrome: a case report | Journal of Medical Case Reports BioMed Central Open Access Rectal mucosal prolapse syndrome as an unusual gastrointestinal manifestation of Sjogren s syndrome a case report Hideki Koga 1 Kayoko Shimizu2 Ken-ichi Tarumi2 Yoshito Sadahira3 Takayuki Matsumoto1 Mitsuo Iida1 and Ken Haruma2 Address Department of Medicine and Clinical Science Graduate School of Medical Sciences Kyushu University Maidashi Higashi-ku Fukuoka 812-8582 Japan 2Division of Gastroenterology Department of Medicine Kawasaki Medical School Japan and 3Department of Pathology Kawasaki Medical School Matsushima Kurashiki 701-0192 Japan Email Hideki Koga - kogahide@ Kayoko Shimizu - shimi@ Ken-ichi Tarumi - doronpa@ Yoshito Sadahira - sadapath@ Takayuki Matsumoto - kogahide@ Mitsuo lida - iidam@ Ken Haruma - kharuma@ Corresponding author Published 30 October 2009 Received 19 September 2009 Journal of Medical Case Reports 2009 3 85 doi l752-l947-3-85 Accepted 30 October 2009 This article is available from http content 3 l 85 2009 Koga et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Abstract Introduction Rectal mucosal prolapse syndrome histologically characterized by fibromuscular obliteration in the lamina propria hyperplastic glands and thickened muscularis mucosa causes rectal bleeding. Sjogren s syndrome is an autoimmune exocrinopathy that chiefly destroys the salivary and lacrimal glands by lympho-plasmacytic infiltration. Although various gastrointestinal manifestations have been reported in patients with Sjogren s syndrome there have not been to our .