Spontaneous splenic rupture and Anisakis appendicitis presenting as abdominal pain: a case report
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  • 作者:Joaquín Valle (1)
    Elisa Lopera (1)
    María Eugenia Sánchez (2)
    Rocío Lerma (3)
    Javier López Ruiz (4)
  • 刊名:Journal of Medical Case Reports
  • 出版年:2012
  • 出版时间:December 2012
  • 年:2012
  • 卷:6
  • 期:1
  • 全文大小:637KB
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  • 作者单位:Joaquín Valle (1)
    Elisa Lopera (1)
    María Eugenia Sánchez (2)
    Rocío Lerma (3)
    Javier López Ruiz (4)

    1. Department of Emergency Medicine, Hospital “Valle de los Pedroches,-Calle Juan Del Rey Calero, S/N, Pozoblanco, 14400, Córdoba, Spain
    2. Department of Pathology, Hospital “Valle de los Pedroches,-Calle Juan Del Rey Calero, S/N, Pozoblanco, 14400, Córdoba, Spain
    3. Department of Radiology, Hospital ,“Valle de los Pedroches,,-Calle Juan Del Rey Calero, S/N, Pozoblanco, 14400, Córdoba, Spain
    4. Department of Surgery, Hospital ,“Valle de los Pedroches,,-Calle Juan Del Rey Calero, S/N, Pozoblanco, 14400, Córdoba, Spain
文摘
Introduction Anisakidosis, human infection with nematodes of the family Anisakidae, is caused most commonly by Anisakis simplex. Acquired by the consumption of raw or undercooked marine fish or squid, anisakidosis occurs where such dietary customs are practiced, including Japan, the coastal regions of Europe and the United States. Rupture of the spleen is a relatively common complication of trauma and many systemic disorders affecting the reticuloendothelial system, including infections and neoplasias. A rare subtype of rupture occurring spontaneously and arising from a normal spleen has been recognized as a distinct clinicopathologic entity. Herein we discuss the case of a woman who presented to our institution with appendicitis secondary to Anisakis and spontaneous spleen rupture. Case presentation We report the case of a 53-year-old Caucasian woman who presented with hemorrhagic shock and abdominal pain and was subsequently found to have spontaneous spleen rupture and appendicitis secondary to Anisakis simplex. She underwent open surgical resection of the splenic rupture and the appendicitis without any significant postoperative complications. Histopathologic examination revealed appendicitis secondary to Anisakis simplex and splenic rupture of undetermined etiology. Conclusions To the best of our knowledge, this report is the first of a woman with the diagnosis of spontaneous spleen rupture and appendicitis secondary to Anisakis simplex. Digestive anisakiasis may present as an acute abdomen. Emergency physicians should know and consider this diagnosis in patients with ileitis or colitis, especially if an antecedent of raw or undercooked fish ingestion is present. Spontaneous rupture of the spleen is an extremely rare event. Increased awareness of this condition will enhance early diagnosis and effective treatment. Further research is required to identify the possible risk factors associated with spontaneous rupture of the spleen.

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