{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T20:04:52Z","timestamp":1649189092871},"reference-count":9,"publisher":"Index Copernicus","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pol Przegl Chir"],"published-print":{"date-parts":[[2019,12,9]]},"abstract":"<jats:p>Introduction: Spontaneous Cholecystocutaneous Fistula occurs as a result of complication from untreated gall bladder stone disease infrequently seen in surgical practice due to early diagnosis of gall stone disease with imaging and appropriate and prompt antibiotic and surgical treatment. Case report: We report our experience with a 40-year-old woman who presented with a yellowish discharge from the umbilicus. Abdominal examination revealed a sinus opening at the umbilicus with the yellowish discharge and a vague mass in the right hypochondrium. CT fistulogram showed tract extending form the umbilicus to the gall bladder. Open cholecystectomy with excision of the fistulous tract was carried out. Histopathological examination showed chronic inflammation of the gall bladder with the fistulous tract lined by inflammatory granulation tissue. Post-operative recovery was normal and uneventful. The patient was normal in follow-up. Cholecystocutaneous fistula is a rare clinical entity. The diagnosis is established with CT and MRCP. Surgery remains the mainstay of treatment.\n\n<\/jats:p>","DOI":"10.5604\/01.3001.0013.6277","type":"journal-article","created":{"date-parts":[[2019,12,9]],"date-time":"2019-12-09T11:39:50Z","timestamp":1575891590000},"page":"62-65","source":"Crossref","is-referenced-by-count":0,"title":["Spontaneous Cholecystocutaneous Fistula: A rare clinical Entity"],"prefix":"10.5604","volume":"93","author":[{"given":"Amit","family":"Gupta","sequence":"first","affiliation":[{"name":"Department of Surgery, All India Institute of Medical Sciences, Rishikesh, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Manoj","family":"Joshua","sequence":"additional","affiliation":[{"name":"Department of Surgery, All India Institute of Medical Sciences, Rishikesh, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Navin","family":"Kumar","sequence":"additional","affiliation":[{"name":"Department of General Surgery, All India Institute of Medical Sciences, Rishikesh, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Udit","family":"Chauhan","sequence":"additional","affiliation":[{"name":"Department of Radiology, All India Institute of Medical Sciences, Rishikesh, India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sweety","family":"Gupta","sequence":"additional","affiliation":[{"name":"Department of Radiation Oncology, All India Institute of Medical Sciences, Rishikesh, India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"3689","reference":[{"key":"195097r1","unstructured":"Schippers H.J.W., Toorenvliet B.R.: A late complication of cholecystitis. NedTijdschr Geneeskd., 2018; 22: 162."},{"key":"195097r2","doi-asserted-by":"crossref","unstructured":"Wang Y.F., Chen H.Q.: Hepatobiliary and Pancreatic: Spontaneous cholecystocutaneousfistula. J Gastroenterol Hepatol., 2019; 34(1): 11.","DOI":"10.1111\/jgh.14285"},{"key":"195097r3","doi-asserted-by":"crossref","unstructured":"Rinzivillo N.M.A., Danna R., Leanza V., Lodato M., Marchese S. et al.: CaseReport: Spontaneous cholecystocutaneous fistula, a rare cholethiasis complication.F1000Research., 2017; 6: 1768.","DOI":"10.12688\/f1000research.12235.1"},{"key":"195097r4","unstructured":"Shinde R., Chatterjee A., Chattopadhyay B.: Cholecystocutaneous Fistula \u2013 ARare Presentation, 2014; 1(5): 242\u2013244."},{"key":"195097r5","doi-asserted-by":"crossref","unstructured":"Gerrard A., Date R.: Delayed Spontaneous Passage of Gallstones via CholecystocutaneousFistula. ACG case reports J., 2017; 4: e102.","DOI":"10.14309\/crj.2017.102"},{"key":"195097r6","doi-asserted-by":"crossref","unstructured":"Maynard W., McGlone E.R., Deguara J.: Unusual aetiology of abdominal wallabscess: cholecystocutaneous fistula presenting 20 years after open subtotalcholecystectomy. BMJ, 2016; 2016: bcr2015213326.","DOI":"10.1136\/bcr-2015-213326"},{"key":"195097r7","doi-asserted-by":"crossref","unstructured":"Sayed L., Sangal S., Finch G.: Spontaneous cholecystocutaneous fistula: a rarepresentation of gallstones. J Surg case reports., 2010; 5: 5.","DOI":"10.1093\/jscr\/2010.5.5"},{"key":"195097r8","doi-asserted-by":"crossref","unstructured":"Kapoor Y., Singh G., Khokhar M.: Spontaneous cholecystocutaneous fistula--not an old time story. Indian J Surg., 2013; 75(Suppl. 1): 188\u2013191.","DOI":"10.1007\/s12262-012-0560-2"},{"key":"195097r9","unstructured":"Malik A.H., Nadeem M., Ockrim J.: Complete laparoscopic management ofcholecystocutaneous fistula. Ulster Med J., 2007; 76(3): 166\u2013167."}],"container-title":["Polish Journal of Surgery"],"original-title":[],"link":[{"URL":"https:\/\/ppch.pl\/gicid\/pdf\/01.3001.0013.6277","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/ppch.pl\/gicid\/pdf\/01.3001.0013.6277","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,5]],"date-time":"2021-05-05T11:34:25Z","timestamp":1620214465000},"score":1,"resource":{"primary":{"URL":"https:\/\/ppch.pl\/gicid\/01.3001.0013.6277"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,12,9]]},"references-count":9,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2021,2,11]]}},"URL":"https:\/\/doi.org\/10.5604\/01.3001.0013.6277","relation":{},"ISSN":["0032-373X","2299-2847"],"issn-type":[{"value":"0032-373X","type":"print"},{"value":"2299-2847","type":"electronic"}],"subject":[],"published":{"date-parts":[[2019,12,9]]}}}