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esophageal achalasia/vomiting

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Vomiting and feeling fat--coincidence of achalasia and bulimia nervosa.

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OBJECTIVE In clinical practice it is often difficult to distinguish between organic and psychological vomiting. METHODS We present a case of a 34-year-old woman with an 18-month history of vomiting with the initial diagnosis of bulimia nervosa (BN). However, the patient showed an unusual vomiting

[Vomiting and denutrition caused by inspiratory achalasia of the cardia].

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[Uncontrollable vomiting of pregnancy symptomatic of unrecognized cardiospasm].

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An unusual case of vomiting and weight loss in pregnancy -- Oesophageal achalasia.

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Esophageal involvement in congenital Chagas' disease. Report of a case with megaesophagus.

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A full-term infant developed dysphagia, vomiting, and regurgitation immediately after birth. On examination at 5 months of age, he was malnourished and had radiographically proven megaesophagus. On direct examination his blood was positive for Trypanosoma cruzi. Additionally an enzyme immunoassay

Intramural esophageal bronchogenic cyst mimicking achalasia in a toddler.

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Bronchogenic cysts are congenital malformations of the tracheobronchial tree. We describe a 20-month-old male who presented with persistent non-bilious emesis; manometry and imaging were consistent with esophageal achalasia. During a planned laparoscopic Heller myotomy, an intramural bronchogenic

Childhood achalasia in Zaria, Nigeria.

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OBJECTIVE To study the presentation, management and outcome of achalasia of the oesophagus in children. METHODS A retrospective case study. METHODS Ahmadu Bello University Teaching Hospital, Zaria, Nigeria. METHODS Seven children managed for achalasia of the oesophagus in a period of 19

[Efficacy and safety of peroral endoscopic myotomy in the treatment of achalasia cardia].

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OBJECTIVE To evaluate the efficacy and safety of peroral endoscopic myotomy (POEM) for achalasia cardia (AC). METHODS A total of 62 patients with AC were enrolled and treated with POEM in the Third Xiangya Hospital, Central South University from April 2012 to October 2014. The symptoms and

Esophageal Achalasia: An Uncommon Complication during Pregnancy Treated Conservatively.

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A 38-year-old Caucasian woman, gravida 3 para 2, was admitted at 29 weeks of gestation because of vomiting, dysphagia for solids and liquids, and loss of weight. An enlargement of the anterior left neck region was noted on the palpation of the thyroid gland. An MRI of the neck showed a marked

Spontaneous perforation of the esophagus in a patient with achalasia.

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Esophageal perforation in achalasia is rare. The risk would mainly follow pneumatic dilatation, and spontaneous perforation has not been described. We report a case of spontaneous rupture of the midesophagus in a 56-year-old woman with treated achalasia in whom the perforation occurred during a meal

Carcinoma in situ within an area of Barrett esophagus in a dog with megaesophagus.

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A 10-y-old Irish Setter was presented with a history of recurrent episodes of regurgitation and vomiting, with more recent development of tachypnea. Megaesophagus had been diagnosed in the dog 2 y prior to this presentation. A solitary polypoid mass present immediately rostral to the lower

Efficacy of the transthoracic modified Heller myotomy in children with achalasia--a 21-year experience.

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From 1974 to 1995, 19 children with achalasia of the esophagus have been treated at our institution. Presenting symptoms included vomiting (n = 14), dysphagia (n = 13), failure to thrive (n = 6), and odynophagia (n = 1). Diagnosis was established by a barium swallow in 19, with eight also undergoing

Spontaneous pneumomediastinum due to achalasia: a case report.

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Spontaneous pneumomediastinum (SPM) is a rare and benign clinical entity characterized by free air around mediastinal structures. Precipitating factors include violent cough, asthma, inhalational drugs, labor and exercise. We report a case of SPM due to achalasia which to the best of our knowledge,

[Practice guideline of peroral endoscopic myotomy of achalasia: Zhongshan experience].

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Peroral endoscopic myotomy (POEM) is a novel clinical technique developed in 2010, and has been widely accepted for treating achalasia and esophageal motility disorders, because of its minimal invasiveness and good efficacy. Zhongshan Hospital has published the practice guideline (the

Successful treatment of achalasia in childhood by pneumatic dilatation.

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Ten consecutive patients (ages 10 to 17) with achalasia of the esophagus diagnosed by radiographic, manometric, and endoscopic criteria were treated by forceful dilatations of the lower esophageal sphincter. A good to excellent response was seen in eight of the ten patients, manifested by
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