| Literature DB >> 12928855 |
Atsushi Muraoka1, Nobuyuki Watanabe, Yoshihiro Ikeda, Yasutaka Kokudo, Akihiko Tatemoto, Yoshiyuki Sone, Shigeo Kagawa, Makoto Tsumura, Masaki Tsuruno, Junichi Kageyama, Kanji Kojima, Koichi Mizobuchi.
Abstract
We report the rare case of a gallbladder cyst arising from the foregut remnants. A 36-year-old woman was referred to our hospital after screening ultrasonography (US) detected a tumor in the gallbladder. On admission, she was well and her blood analyses were all normal. US showed a cystic mass with internal high-echoic lesions, and computed tomography (CT) demonstrated a protruding tumor with slight enhancement in the gallbladder. Angiography provided no additional information; however, sequential CT-arteriography (CTA) clearly demonstrated that this tumor was a cystic lesion. Surgical exploration was performed, first because of the difficulty in establishing a definite diagnosis, and also because the patient wanted the tumor removed. The resected specimen contained a unilocular cystic tumor that looked like a submucosal tumor. Histologically, the wall of the cyst was lined by ciliated stratified columnar epithelium with interspersed goblet cells and underlying smooth muscle fibers. The mass was finally diagnosed as a congenital ciliated foregut cyst of the gallbladder. Cysts of the gallbladder are uncommon and the majority are acquired. To our knowledge, this represents only the fourth report of a ciliated foregut cyst of the gallbladder in the literature. Although rare, an awareness of this entity could allow a preoperative diagnosis to be made, whereby surgical exploration may be avoided. CT-A is a very useful diagnostic tool, especially when the nature of the tumor presents a difficult differential diagnosis.Entities:
Mesh:
Year: 2003 PMID: 12928855 DOI: 10.1007/s00595-002-2555-2
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549