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dc.contributor.authorDiktas, Husrev
dc.contributor.authorGorenek, Levent
dc.contributor.authorFiliz, Ali Ilker
dc.contributor.authorKivanc, Mert
dc.contributor.authorOncul, Oral
dc.contributor.authorAcar, Ali
dc.contributor.authorSucullu, Ilker
dc.contributor.authorBaylan, Orhan
dc.date.accessioned2021-03-03T12:30:17Z
dc.date.available2021-03-03T12:30:17Z
dc.date.issued2010
dc.identifier.citationAcar A., Sucullu I., Baylan O., Filiz A. I. , Diktas H., Kivanc M., Oncul O., Gorenek L., "Coexistence of pancreatic tuberculosis with systemic brucellosis: a case report", CENTRAL EUROPEAN JOURNAL OF MEDICINE, cilt.5, sa.5, ss.573-576, 2010
dc.identifier.issn1895-1058
dc.identifier.othervv_1032021
dc.identifier.otherav_2e7336cc-391e-43bb-90cc-484d597c9f3c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/35778
dc.identifier.urihttps://doi.org/10.2478/s11536-009-0143-1
dc.description.abstractIsolated pancreatic tuberculosis is an extremely rare clinical entity and is difficult to diagnose particularly in immunocompetent individuals. Clinical findings and symptomatology of brucellosis are often similar to tuberculosis thus making the differentiation amongst the two entities difficult. We report a case of pancreatic tuberculosis with systemic brucellosis in a 29 year old veterinarian who presented with epigastric pain and loss of appetite. Initial investigations revealed leukocytosis with moderately elevated transaminase, gamma glutamyl transferase, amylase and lipase levels. Imaging studies revealed an anechoic multiloculated cyst in the body and tail of the pancreas. Given the patient's occupational risk coupled with the presence of a positive Brucella agglutination test (with a titer of 1:320); a diagnosis of pancreatitis secondary to brucellosis was given. In addition to standard pancreatitis therapy of bowel rest with intravenous fluid/electrolyte replacement, anti-brucellosis therapy was also administered. The patient's initial response to therapy was positive however, 6 weeks into therapy, his abdominal pain recurred and repeat CT scan revealed the development of a pseudocyst in the pancreas. After failing a second attempt at conservative supportive therapy, the patient underwent an explorative laparotomy. Histological examination of the resected pancreatic specimen showed necrosis and was positive for tuberculosis by polymerase chain reaction. Herein, we describe the first case reported in the medical literature of the coexistence of systemic brucellosis with pancreatic tuberculosis. We suggest that the possibility of the coexistence of brucellosis with tuberculosis be kept in mind when assessing pancreatitis patients in endemic regions and in individuals with occupational risk hazards.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectTemel Tıp Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.titleCoexistence of pancreatic tuberculosis with systemic brucellosis: a case report
dc.typeMakale
dc.relation.journalCENTRAL EUROPEAN JOURNAL OF MEDICINE
dc.contributor.departmentGulhane Military Medical Academy , ,
dc.identifier.volume5
dc.identifier.issue5
dc.identifier.startpage573
dc.identifier.endpage576
dc.contributor.firstauthorID2209385


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