A Rare Case of Gastrointestinal Obstruction: Bouveret Syndrome
نویسندگان
چکیده
منابع مشابه
Bouveret syndrome: A fatal diagnostic dilemma of gastric outlet obstruction.
The patient presented in this study was a 54-year-old woman complaining of nausea and vomiting, onset preceding four days, with no significant past medical history and an unremarkable surgical history. The patient was afebrile and hypertensive. Physical examination revealed a non-tender abdomen, and initial laboratory evaluation revealed elevated blood glucose level, ketonuria, leukocytosis, el...
متن کاملA Rare Case of Intestinal Obstruction due to Taenia Saginata
Intestinal obstruction may be duo to various mechanical or functional reasons. Worms, especially Ascaris worms are one of the mechanical reasons of intestinal obstruction. Obstruction due to Taenia saginata is a rare phenomenon. Here we report a case of intestinal obstruction due to Taenia saginata infection in a 30 year-old male patient undergoing laparatomy with the diagnosis of intestinal ob...
متن کاملGastric outlet obstruction due to gall stones (Bouveret syndrome).
Gastric outlet obstruction by gall stone is a rare complication of a common disorder. Two cases are reported here. The investigations are conducted along the same lines as for pyloric stenosis. The diagnosis can be made with a barium meal or gastroscopy. Treatment is by surgical intervention after adequate resuscitation.
متن کاملA Rare Case of Budd Chiari Syndrome in a Child
A 7-year- old male child presented with the complaints of tense abdominal distension and swelling over feet since 1 month. The patient had repeated episodes of similar complaints since last two years with partial or complete relief after taking various forms of allopathic therapy. On imaging, Budd-Chiari syndrome was diagnosed which was hallmarked by occluded Inferior venacava (IVC), caudate lo...
متن کاملPrepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report
Klinefelter syndrome is characterised by advancing testicular function deterioration causing aspermatogenesis and androgen deficiency. Klinefelter patients characteristically have complete male sex differentiation, and genital anomalies are infrequently associated. Penoscrotal malformations at birth are very rare in this syndrome. Nonetheless, it is important to know the association, as one 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: Journal of Gastrointestinal & Digestive System
سال: 2015
ISSN: 2161-069X
DOI: 10.4172/2161-069x.1000277