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subcutaneous emphysema/vomă

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Vomiting-induced surgical emphysema and pneumomediastinum: a self-remitting or life-threatening condition?

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A previously well 18-year-old male presented with a 3-day history of vomiting, abdominal pain and increasing neck swelling. X-rays demonstrated both pneumomediastinum and cervical surgical emphysema and initial efforts were centred upon excluding Boerhaave syndrome (vomiting-induced oesophageal

Subcutaneous emphysema following severe vomiting after emerging from general anesthesia.

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Postoperative nausea and vomiting-related subcutaneous emphysema is an unexpected complication, especially after uneventful surgery and anesthesia. Here we report and discuss two cases of subcutaneous emphysema following severe retching and vomiting which resolved spontaneously after several days.

[Subcutaneous emphysema caused by postoperative vomiting].

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The authors present 3 cases of subcutaneous emphysema after postoperative vomiting treated during a 4-year period. All patients were female, they underwent positioning during general anaesthesia--rotation on their abdomen and they vomited postoperatively with subsequent development of subcutaneous

Pneumomediastinum, bilateral pneumothorax, pleural effusion, and surgical emphysema after routine apicectomy caused by vomiting.

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Mediastinal and subcutaneous emphysema may occur after dental and oral surgery as a result of iatrogenic introduction of air or injury to the tracheobronchial tree. We report a patient who developed emphysema and pneumothorax after dentoalveolar surgery, which made diagnosis and management

Delayed surgical emphysema, pneumomediastinum and bilateral pneumothoraces after postoperative vomiting.

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We describe a case of surgical emphysema, pneumomediastinum and bilateral pneumothoraces which occurred some hours after general anaesthesia for a repeat laparoscopy and followed persistent nausea and vomiting. We report the case because of the unexpected and delayed appearance, which led to delay

Vomiting-induced pneumomediastinum and subcutaneous emphysema does not always indicate Boerhaave's syndrome: report of six cases.

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Spontaneous pneumomediastinum is an uncommon, self-limiting condition resulting from alveolar rupture in young adults. Because of the ambiguous presentation and the general lack of awareness of this condition, its diagnosis is often delayed, missed, or confused with spontaneous esophageal

Subcutaneous emphysema in vomiting of pregnancy.

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A case of subcutaneous emphysema following post-operative vomiting.

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Mediastinal and subcutaneous emphysema in diabetic coma with vomiting.

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Massive subcutaneous emphysema and sudden airway compromise after postoperative vomiting.

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Vomiting-induced pneumomediastinum as a result of recurrent Boerhaave's syndrome

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Vomiting-induced pneumomediastinum can be a result of barotrauma causing alveolar rupture or Boerhaave's syndrome. Although a rare cause of secondary pneumomediastinum, Boerhaave's syndrome allows extravasation of air and fluid due to oesophageal perforation. We report a case of a 20-year-old female

Vomiting in pregnancy resulting in oesophageal perforation in a 15-year-old.

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Spontaneous perforation of the oesophagus is extremely rare in children, as is perforation due to vomiting in pregnancy. We report the case of a 15-year-old in whom vomiting in early pregnancy resulted in oesophageal perforation with subcutaneous emphysema causing marked facial swelling in the

Postpartum pneumomediastinum manifested by surgical emphysema. Should we always worry about underlying oesophageal rupture?

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Spontaneous pneumomediastinum during labour is a rare, usually benign and self-limiting condition. It often presents with chest or neck pain and surgical emphysema. The latter sign is easy to demonstrate but often missed during clinical assessment if the condition is not included in the differential
Background: Previous literature on epidural pneumatosis (pneumorrhachis, or air in epidural cavity) associated with forceful vomiting in a patient with diabetic ketoacidosis (DKA) has consisted of individual case reports without
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