Rapunzel syndrome in a 7-year-old boy: A case report
نویسندگان
چکیده
منابع مشابه
Pediatric acute-onset neuropsychiatric syndrome in a 6.5-year-old boy: A case report
Background: “Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections”, or PANDAS, is a syndrome characterized by acute-onset obsessive-compulsive disorder (OCD) and/or tics accompanied by the neuropsychiatric symptoms. This case is reported because of its rarity. Case report: A 6.5-year-old boy with swollen tonsils, high-grade fever and rash was admitted to Ami...
متن کامل'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 کاملXanthogranulomatous pyelonephritis report of a case in a 5 year old boy
Xanthogranulomatous pyelonephritis is an unusual type of the kidney infection which is characterized by infiltration of mononuclear inflammatory cells and lipid laden macrophages ( foam cells). It is manifested by a firm, lobulated and yellowish kidney mass which is difficult to differentiate from renal cell carcinoma grossly. Six out of 1000 cases of cryonic pyelonephritis which are treated su...
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...
متن کاملAutoimmune Polyglandular Syndrome Type 2 (APS-2) in a 70-Year-Old Woman: A Case Report
Type2 autoimmune polyglandular (Schmidt) syndrome is defined by the occurrence of at least 2 out of 3 of the following manifestations, Addison's disease, Hypothyroidism and Type 1 diabetes mellitus. APS2 is a rare condition with an incidence of 1–2/100 000 per year. Prevalence of APS-2 is most happening in the range of 20-40 years of age. Here we present a patient who complained about loss of ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International Journal of Surgery Science
سال: 2019
ISSN: 2616-3462,2616-3470
DOI: 10.33545/surgery.2019.v3.i4i.298