Rapunzel Syndrome: A Rare Presentation with Giant Gastric Ulcer
نویسندگان
چکیده
منابع مشابه
Rapunzel Syndrome: A Rare Presentation with Giant Gastric Ulcer
The Rapunzel syndrome refers to an uncommon and rare form of trichobezoar that extends past the stomach into the small intestines. The Rapunzel syndrome is usually found in young female patients with a history of psychiatric disorders, mainly trichotillomania and trichophagia. We describe a case of Rapunzel syndrome in a 15-year-old girl who presented with abdominal pain, vomiting, and weight l...
متن کاملThe Rapunzel syndrome: a rare presentation of trichobezoar.
CASE HISTORY A five-year old girl was admitted in 1985 with an eight-day history of epigastric pain and vomiting. The pain was occasional and not severe. She had lost weight, to 13-1 kg, and was pale and thin. There was a tender epigastric mass. The haemoglobin concentration was 12-8 g/dl. Her mother said the child regularly pulled and ate the sleeves of her cardigans. An ultrasound scan showed...
متن کاملRapunzel Syndrome: A Rare Postpartum Case
The Rapunzel syndrome describes a disorder in which a significant amount of hair is swallowed, forming a trichobezoar that extends past the stomach into the small intestines. Given the indigestible nature of hair, it subsequently leads to obstruction within the gastrointestinal system. Clinically, patients may present with symptoms of gastrointestinal obstruction, including abdominal complaints...
متن کاملGiant gastric trichobezoar in a young female with Rapunzel syndrome: case report
Rapunzel syndrome is an extremely rare complication of a gastric trichobezoar in. We report here the unusual case of a case of a 16 years old girl presented with severe abdominal pain and vomiting. Clinical examination revealed a malnourished girl, with presence of a mobile and sensitive abdominal mass of 20x15 cm witch filled the upper quadrant. An abdominal computed tomography scan showed a h...
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ژورنال
عنوان ژورنال: Case Reports in Medicine
سال: 2014
ISSN: 1687-9627,1687-9635
DOI: 10.1155/2014/267319