First sliding Amyand hernia harbouring appendicular schistosomiasis: Case reportShow others and affiliations
2019 (English)In: International Journal of Surgery Case Reports, E-ISSN 2210-2612, Vol. 63, p. 143-146Article in journal (Refereed) Published
Abstract [en]
Introduction: Amyand's hernia (AH) is rare, schistosomiasis of the appendix is very uncommon, and both conditions coexisting together is an extremely rare event. Pre-operative diagnosis of each of the two conditions is usually difficult. To the best of our knowledge, the current paper is first to report both these two conditions in coexistence. Presentation of case: A 31-year old man who had no comorbidities was admitted electively as a day case of non-complicated right indirect inguinal hernia. Further history and physical examination were unremarkable. Intraoperatively the patient was found to have right sliding AH with appendicular schistosomiasis (AS). The patient underwent Lichtenstein repair of the hernia with appendectomy. On follow up he was referred to infectious disease clinic, and the post-operative course was uneventful. Conclusions: Intraoperative identification of non-typical hernia sac before its opening should alert the surgeon to the possibility of sliding hernia and the presence of an organ as a part of the sac. Rare causes of appendicular masses like schistosomiasis granuloma should be considered in endemic areas or immigrants from these areas, despite the difficulty of preoperative diagnosis. Management should follow general guidelines of appendectomy, hernia repair and dealing with the associated pathology if present.
Place, publisher, year, edition, pages
Elsevier, 2019. Vol. 63, p. 143-146
Keywords [en]
Case report, Inguinal hernia, Intestinal schistosomiasis, Tropical disease
National Category
Surgery Health Care Service and Management, Health Policy and Services and Health Economy Gastroenterology and Hepatology
Research subject
Individual and Society VIDSOC
Identifiers
URN: urn:nbn:se:his:diva-17781DOI: 10.1016/j.ijscr.2019.09.014ISI: 000493909500033PubMedID: 31585325Scopus ID: 2-s2.0-85072758444OAI: oai:DiVA.org:his-17781DiVA, id: diva2:1359991
2019-10-102019-10-102024-01-17Bibliographically approved