Rapunzel Syndrome Case Report: A 13-year-old Girl
نویسندگان
چکیده
منابع مشابه
'Rapunzel syndrome' trichobezoar in a 7-year-old girl: a case report
BACKGROUND Rapunzel syndrome is a rare type of trichobezoar with an extension of the hair into the small bowel. Clinical presentation is deceptive and vague ranging from abdominal mass to gastrointestinal symptoms. CASE PRESENTATION We present a 7 years old girl with Rapunzel syndrome, where the trichobezoar was not suspected at all especially with negative history of trichophagia. In majorit...
متن کاملRapunzel Syndrome - Trichobezoar in a 9 Year Old Girl: A Case Report
We here report a case of 9 years old girl presented in casualty with an acute abdomen and small bowel obstruction and on laprotomy a large trichobezoar was revealed extending into small intestine along with intussuception. Rapunzel syndrome is a rare but potentially fatal trichobezoar. Trichobezoar, an underdiagnosed entity, has to be considered in the differential diagnosis of abdominal pain a...
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Abstract Acute inflammation of the gallbladder can occur without gallstones. Acalculous cholecystitis typically develops in critically ill patients in the intensive care unit. Patients on parenteral nutrition, with extensive burns, sepsis, major operations, multiple organ trauma or prolonged illness with multiple organ system failure are at risk for developing acalculous cholecystitis. The ass...
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BACKGROUND SHORT syndrome is a rare genetic congenital defects condition. The frequency of the disease still remains unknown. CASE PRESENTATION We report the two-year-four-month old female with SHORT syndrome who present growth retardation and dysmorphic features (triangular-shaped face, prominent forehead, ocular depression, lipodystrophy at the lumbar region and around elbows), consistent w...
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Prolidase deficiency is a rare autosomal recessive disorder characterized by recurrent and nonhealing skin ulcers along with facial dysmorphism and mental retardation. We report a 13-year-old girl who has clinical manifestation of Proliodase deficiency. It is a very rare disorder and no such case has been reported so far from Pakistan.
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ژورنال
عنوان ژورنال: International Journal of Trichology
سال: 2012
ISSN: 0974-7753
DOI: 10.4103/0974-7753.111202