Progressive disseminated histoplasmosis presenting like chronic parenchymal liver disease with ascites: a rare case report and discussion.

dc.contributor.authorBanerjee, Arnab
dc.date.accessioned2015-11-12T09:23:20Z
dc.date.available2015-11-12T09:23:20Z
dc.date.issued2014-10
dc.description.abstractA 82 year old diabetic and hypertensive Muslim man presented with ascites along with features of portal hypertension. Though it initially seemed to be a primary case of chronic parenchymal liver disease, investigations revealed it to be a case of Progressive Disseminated Histoplasmosis (PDH) with bilateral adrenomegaly, hepatosplenomegaly and ascites. The ascites was high SAAG in nature and no evidence of malignancy or tuberculosis could be found. The patient was treated with liposomal amphotericin B and was subsequently discharged on oral itraconazole therapy. On follow-up he was found to be significantly better at 3 months.en_US
dc.identifier.citationSushma Maram, Ramalingam Krishnan, Naidu Jupalli N, Lakshmi Tatireddy V. Progressive disseminated histoplasmosis presenting like chronic parenchymal liver disease with ascites: a rare case report and discussion. International Journal of Research in Medical Sciences. 2014 Oct-Dec; 2(4): 1699-1701.en_US
dc.identifier.issn2320-6071
dc.identifier.issn2320-6012
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/165523
dc.language.isoenen_US
dc.source.urihttps://www.msjonline.org/?mno=164531en_US
dc.subjectProgressive disseminated histoplasmosisen_US
dc.subjectAdrenomegalyen_US
dc.subjectAscitesen_US
dc.subjectChronic parenchymal liver diseaseen_US
dc.titleProgressive disseminated histoplasmosis presenting like chronic parenchymal liver disease with ascites: a rare case report and discussion.en_US
dc.typeArticleen_US
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