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Diffuse intestinal ganglioneuromatosis an uncommon manifestation of Cowden syndrome 被引量:5
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作者 Maria Teresa Herranz Bachiller Jesus Barrio Andrés +7 位作者 Fernando Pons Noelia Alcaide Suárez rafael ruiz-zorrilla Lorena Sancho del Val Sara Lorenzo Pelayo Carlos De La Serna Higuera Ramon Atienza Sánchez Manuel Perez Miranda 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2013年第2期34-37,共4页
Diffuse intestinal ganglioneuromatosis is a hamartomatous polyposis characterized by a disseminated, intramural or transmural proliferation of neural elements involving the enteric plexuses. It has been associated wit... Diffuse intestinal ganglioneuromatosis is a hamartomatous polyposis characterized by a disseminated, intramural or transmural proliferation of neural elements involving the enteric plexuses. It has been associated with MEN Ⅱ, neurofibromatosis type 1 and hamartomatous polyposis associated with phosphatase and tensin homolog mutation. We report the case of a female patient with a history of a breast and endometrial tumor who presented in a colonoscopy performed for rectal bleeding diffuse ganglioneuromatosis, which oriented the search for other characteristic findings of Cowden syndrome given the personal history of the patient. The presence of an esophagogastric polyposis was also noted. Cowden syndrome is characterized by skin lesions, but it is rarely diagnosed by these lesions, because they are usually overlooked. Intestinal polyposis is not a major diagnostic criterion but it is very useful for early diagnosis. The combination of colonic polyposis and glucogenic acanthosis should orient the diagnosis to Cowden syndrome. 展开更多
关键词 Ganglioneuromatosis Gastrointestinal poliposis PHOSPHATASE and TENSIN HOMOLOG Cowden síndrome HAMARTOMA
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