dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorLima, Talles Bazeia
dc.creatorDomingues, Maria Aparecida Custódio
dc.creatorCaramori, Carlos Antonio
dc.creatorSilva, Giovanni Faria
dc.creatorOliveira, Cássio Vieira de
dc.creatorYamashiro, Fábio da Silva
dc.creatorFranzoni, Letícia de Campos
dc.creatorSassaki, Lígia Yukie
dc.creatorRomeiro, Fernando Gomes
dc.date2016-07-07T12:33:59Z
dc.date2016-10-25T21:43:48Z
dc.date2016-07-07T12:33:59Z
dc.date2016-10-25T21:43:48Z
dc.date2013
dc.date.accessioned2017-04-06T10:44:24Z
dc.date.available2017-04-06T10:44:24Z
dc.identifierWorld Journal of Gastroenterology, v. 19, n. 34, p. 5750-5753, 2013.
dc.identifier2219-2840
dc.identifierhttp://hdl.handle.net/11449/140470
dc.identifierhttp://acervodigital.unesp.br/handle/11449/140470
dc.identifier10.3748/wjg.v19.i34.5750
dc.identifier2937965588168990
dc.identifierhttp://dx.doi.org/10.3748/wjg.v19.i34.5750
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/950757
dc.descriptionParacoccidioidomycosis is a systemic granulomatous disease caused by fungus, and must be considered in the differential diagnosis of intra-abdominal tumors in endemic areas. We report a rare case of paracoccidioidomycosis in the pancreas. A 45-year-old man was referred to our institution with a 2-mo history of epigastric abdominal pain that was not diet-related, with night sweating, inappetence, weight loss, jaundice, pruritus, choluria, and acholic feces, without signs of sepsis or palpable tumors. Abdominal ultrasonography (US) showed a solid mass of approximately 7 cm × 5.5 cm on the pancreas head. Abdominal computerized tomography showed dilation of the biliary tract, an enlarged pancreas (up to 4.5 in the head region), with dilation of the major pancreatic duct. The patient underwent exploratory laparotomy, and the surgical description consisted of a tumor, measuring 7 to 8 cm with a poorly-defined margin, adhering to posterior planes and mesenteric vessels, showing an enlarged bile duct. External drainage of the biliary tract, Rouxen-Y gastroenteroanastomosis, lymph node excision, and biopsies were performed, but malignant neoplasia was not found. Microscopic analysis showed chronic pancreatitis and a granulomatous chronic inflammatory process in the choledochal lymph node. Acid-alcohol resistant bacillus and fungus screening were negative. Fine-needle aspiration of the pancreas was performed under US guidance. The smear was compatible with infection by Paracoccidioides brasiliensis. We report a rare case of paracoccidioidomycosis simulating a malignant neoplasia in the pancreas head.
dc.languageeng
dc.relationWorld Journal of Gastroenterology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectParacoccidioidomycosis
dc.subjectPancreas
dc.subjectFungus infection
dc.subjectPancreatic tumors
dc.subjectDifferential diagnosis
dc.titlePancreatic paracoccidioidomycosis simulating malignant neoplasia: case report
dc.typeOtro


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