World journal of gastroenterology · 2013
Spontaneous intramural duodenal hematoma in type 2B von Willebrand disease.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Eichele Derrick D, Ross Meredith, Tang Patrick, Hutchins Grant F, Mailliard Mark
Аннотация
Intramural duodenal hematoma is a rare cause of a proximal gastrointestinal tract obstruction. Presentation of intramural duodenal hematoma most often occurs following blunt abdominal trauma in children, but spontaneous non-traumatic cases have been linked to anticoagulant therapy, pancreatitis, malignancy, vasculitis and endoscopy. We report an unusual case of spontaneous intramural duodenal hematoma presenting as an intestinal obstruction associated with acute pancreatitis in a patient with established von Willebrand disease, type 2B. The patient presented with abrupt onset of abdominal pain, nausea, and vomiting. Computed tomography imaging identified an intramural duodenal mass consistent with blood measuring 4.7 cm × 8.7 cm in the second portion of the duodenum abutting on the head of the pancreas. Serum lipase was 3828 units/L. Patient was managed conservatively with bowel rest, continuous nasogastric decompression, total parenteral nutrition, recombinant factor VIII (humateP) and transfusion. Symptoms resolved over the course of the hospitalization. This case highlights an important complication of an inherited coagulopathy.
Предметные рубрики MeSH
Abdominal PainAcute DiseaseBlood TransfusionCoagulantsCombined Modality TherapyDecompressionDuodenal DiseasesDuodenal ObstructionEndoscopy, Digestive SystemEndosonographyFactor VIIIHematomaHumansMaleNauseaPancreatitisParenteral Nutrition, TotalTomography, X-Ray ComputedTreatment OutcomeVomitingYoung Adultvon Willebrand Disease, Type 2