書誌事項
- タイトル別名
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- INCOMPLETE PEUTZ-JEGHERS SYNDROME WITH PSEUDOINVASION OF DUODENAL POLYP: REPORT OF A CASE
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A 37-year-old man was admitted to our hospital for the further examination and therapy of the duodenal tumor. Gastrointestinal endoscopy revealed a large polypoid lesion which had a rough, nodular surface in the duodenal bulb. And at the side of tumor edge, there were elevated lesions like a submucosal tumor. Endoscopic ultrasonography showed a slight hypere-choic mass derived from second to third layers of the duodenal wall. Cystic areas were contained within the tumor. Fine-needle aspiration biopsy was performed. The biopsy speci-men showed epithelial and Brunner's gland cells hyperplasia. Surgical resection was performed in consideration of the tumor size, and duodenal polypoid lesion measured 50× 43× 28mm in size. The tumor was diagnosed histologically as Peutz Jeghers (P-J) polyp with pseudoinvasion in the submucosa to subserosa. Additionally, another hamartomatous polyps were observed in the jejunum and ileum. Neither family history of intestinal polyposis nor muco-cutaneous pigmentation was observed, the case was diagnosed as incomplete Peutz-Jeghers Syndrome.
収録刊行物
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- 日本消化器内視鏡学会雑誌
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日本消化器内視鏡学会雑誌 48 (6), 1221-1227, 2006
一般社団法人 日本消化器内視鏡学会
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キーワード
詳細情報 詳細情報について
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- CRID
- 1390282679194281088
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- NII論文ID
- 130004254962
- 10018198340
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- NII書誌ID
- AN00192102
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- ISSN
- 18845738
- 03871207
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可