Solitary Peutz-Jeghers-type Polyp of the Stomach
نویسندگان
چکیده
منابع مشابه
A giant and extensive solitary Peutz–Jeghers-type polyp in the antrum of stomach
RATIONALE A solitary Peutz-Jeghers-type polyp is a hamartomatous polyp which without either mucocutaneous pigmentation or a family history of Peutz-Jeghers syndrome (PJS). It can occur in all of the gastrointestinal tract, but it is extremely rare in the stomach. PATIENT CONCERNS A 53-year-old man was admitted to the local hospital with left upper abdominal pain lasting 2 weeks. A gastroscopy...
متن کاملSolitary Peutz-Jeghers Polyp in a Paediatric Patient
Hamartomatous polyps of Peutz-Jeghers are mostly found in patients affected by Peutz-Jeghers syndrome (PJS), but they can be rarely encountered in the general population. It is unclear whether a solitary Peutz-Jeghers polyp (PJP) is an incomplete form of PJS or a separate entity. We report a case of solitary PJP in a paediatric patient in whom the other features of PJS were absent. The patient ...
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 کاملA rare case report of A solitary gastric Peutz-Jeghers type polyp.
Peutz-Jegher syndrome (PJS) is a rare, autosomal-dominant disorder characterized by hamartomatous polyps in any part of the alimentary tract, and almost always associated with intestinal polyposis and mucocutaneous pigmentation (1). Rarely, solitary PJP arise inpatients without other features of PJS. A review of the English literature revealed only 6 published cases since 1989. Here, we would l...
متن کاملSolitary Peutz-Jeghers-type hamartomatous polyp as a cause of recurrent acute pancreatitis.
a diagnosis of acute pancreatitis. The patient had experienced abdominal pain, nausea, and vomiting. In the 2 months prior to admission, he had been admitted and treated for acute pancreatitis twice in another hospital. He had no history of alcohol intake or habitual drug use. The physical examination was unremarkable except for epigastric tenderness, but his amylase level was markedly raised (...
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ژورنال
عنوان ژورنال: Internal Medicine
سال: 2020
ISSN: 0918-2918,1349-7235
DOI: 10.2169/internalmedicine.4811-20