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Hemorrhagic shock due to submucosal esophageal hematoma along with mallory-weiss syndrome: A case report

BACKGROUND: Esophageal submucosal hematoma is a rare condition. Although the exact etiology remains uncertain, vessel fragility with external factors is believed to have led to submucosal bleeding and hematoma formation; the vessel was ruptured by a sudden increase in pressure due to nausea, and the...

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Detalles Bibliográficos
Autores principales: Oba, Jiro, Usuda, Daisuke, Tsuge, Shiho, Sakurai, Riki, Kawai, Kenji, Matsubara, Shun, Tanaka, Risa, Suzuki, Makoto, Takano, Hayabusa, Shimozawa, Shintaro, Hotchi, Yuta, Usami, Kenki, Tokunaga, Shungo, Osugi, Ippei, Katou, Risa, Ito, Sakurako, Mishima, Kentaro, Kondo, Akihiko, Mizuno, Keiko, Takami, Hiroki, Komatsu, Takayuki, Nomura, Tomohisa, Sugita, Manabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516938/
https://www.ncbi.nlm.nih.gov/pubmed/36186194
http://dx.doi.org/10.12998/wjcc.v10.i27.9911
Descripción
Sumario:BACKGROUND: Esophageal submucosal hematoma is a rare condition. Although the exact etiology remains uncertain, vessel fragility with external factors is believed to have led to submucosal bleeding and hematoma formation; the vessel was ruptured by a sudden increase in pressure due to nausea, and the hematoma was enlarged by antiplatelet or anticoagulant therapy. Serious conditions are rare, with a better prognosis. We present the first known case of submucosal esophageal hematoma-subsequent hemorrhagic shock due to Mallory-Weiss syndrome. CASE SUMMARY: A 73-year-old female underwent endovascular treatment for an unruptured cerebral aneurysm. The patient received aspirin and clopidogrel before surgery and heparin during surgery, and was well during the surgery. Several hours after returning to the ICU, she complained of chest discomfort, vomited 500 mL of fresh blood, and entered hemorrhagic shock. Esophageal submucosal hematoma with Mallory-Weiss syndrome was diagnosed through an endoscopic examination and computed tomography. In addition to a massive fluid and erythrocyte transfusion, we performed a temporary compression for hemostasis with a Sengstaken-Blakemore (S-B) tube. Afterwards, she became hemodynamically stable. On postoperative day 1, we performed an upper gastrointestinal endoscopy and confirmed no expansion of the hematoma nor any recurring bleeding; therefore, we removed the S-B tube and clipped the gastric mucosal laceration at the esophagogastric junction. We started oral intake on postoperative day 10. The patient made steady progress, and was discharged on postoperative day 33. CONCLUSION: We present the first known case of submucosal esophageal hematoma subsequent hemorrhagic shock due to Mallory-Weiss syndrome.