A 47-year-old male with Peutz Jeghers syndrome and metachronic polypoid lesions
نویسندگان
چکیده
doscopy. A double-balloon enteroscopy was performed for partially obstructive attacks of abdominal pain suspicious of small-bowel invaginations by big polyps; enteroscopy confirmed the diagnosis. A majority of polyps were localized in the jejunum, and a polypectomy of lesions greater than 1 cm was performed. Histology was consistent with harmatomatous polyps. The entire small bowel was explored using the oral route, and the cecum was reached through Bahuin’s valve (Figs. 1 and 2). Double-balloon enteroscopy, described by H. Yamamoto (1,2), is a first-line method small-bowel exploration that complements capsule endoscopy. Yamamoto described the total exploration of the small bowel by the oral route (the anal route is more common in Asian series). However, we have seen no references on the total exploration of the small bowel with this technique in our setting. In a study report of 635 enteroscopies (3) the median length of small bowel explored by double-balloon enteroscopy was 270 cm for the oral route and 150 cm for the anal route. Generally, a total exploration of the small bowel is possible using both the oral route and anal route in the same patient (4), but we found no references about the total exploration of the small bowel with this technique in our setting.
منابع مشابه
Giant solitary gastric Peutz-Jeghers polyp mimicking a malignant gastric tumor: the largest described in literature.
A solitary Peutz-Jeghers polyp is defined as a unique polyp occurring without associated mucocutaneous pigmentation or a family history of Peutz-Jeghers syndrome. Gastric solitary localization is a rare event, with only eight reported cases to date. We report herein the case of a 43-year old woman who presented with upper gastrointestinal bleeding, severe anemia, weight loss and asthenia. Endos...
متن کاملJejunoduodenal intussusception caused by a solitary polyp in a woman with Peutz-Jeghers syndrome: a case report
INTRODUCTION Peutz-Jeghers syndrome is a rare autosomal dominant disorder characterized by hamartomatous polyps and characteristic mucocutaneous pigmentation. The hamartomatous polyps of Peutz-Jeghers syndrome can cause intestinal occlusion, especially in the small intestine. Intussusception is seen frequently in children, but rarely in adults. CASE PRESENTATION We present the case of a 21-ye...
متن کاملA 21-year-old female patient with Peutz-Jeghers syndrome.
The paper describes a case of a 21-year-old woman admitted to the Department of Internal Medicine with signs and symptoms of microcytic anemia. The presence of characteristic skin lesions, results of laboratory tests and positive family history led to the diagnosis of a rare colonic polyposis, Peutz-Jeghers syndrome. The article presents also history, symptomatology, recommended tests and treat...
متن کاملA solitary Peutz-Jeghers type polyp in the jejunum of a 19 year-old male
A 19-year old male presented with melena and anemia. A duodenoscopy revealed no abnormalities, but a small bowel X-ray series demonstrated a large jejunal polyp. This 4 cm large polyp was visualised during peroperative small bowel endoscopy and was subsequently surgically removed. The polyp had the characteristic histologic appearance of a Peutz-Jeghers type polyp, but the patient had no other ...
متن کاملPeutz - Jeghers syndrome associated with gastrointestinal carcinoma
Patients with the Peutz-Jeghers syndrome carry a slight, though definite, increased risk of gastrointestinal carcinoma.The malignant potentiality of Peutz-Jeghers hamartomatous polyps, generally considered benign, is supported by this report. Two cases of metastasising gastrointestinal carcinoma associated with the Peutz-Jeghers syndrome are described in a 56 year old female and her 29 year old...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2007