Incidental diagnosis of renal tuberculosis in an adolescent submitted to videolaparoscopic nefrectomy

Genitourinary tuberculosis is rare in children. The aim of this study is to describe an unusual case of renal tuberculosis in a 16 years old girl, diagnosed with Hinman Syndrome and chronic renal failure. During a hematuria investigation the cystourethrogram revealed grade V right vesicoureteral ref...

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Published inPediatric Urology Case Reports Vol. 3; no. 5; p. 158
Main Authors Talini, Carolina, Neves de Carvalho, Bruna Cecília, Silveira, Antonio Ernesto da, Amarante, Antonio Carlos Moreira, Antunes, Letícia Alves
Format Journal Article
LanguageEnglish
Published Prof. Dr. Hayrettin Öztürk 01.09.2016
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Summary:Genitourinary tuberculosis is rare in children. The aim of this study is to describe an unusual case of renal tuberculosis in a 16 years old girl, diagnosed with Hinman Syndrome and chronic renal failure. During a hematuria investigation the cystourethrogram revealed grade V right vesicoureteral reflux and small bladder. Ultrasonography demonstrated various cysts in left kidney with irregular content, suggesting dysplastic multicystic kidney. Scintigraphy showed functional exclusion of the left kidney. Total laparoscopic nephrectomy was proposed. Gregoir right ureteral reimplantation and Mitrofanoff mechanism using the distal left ureter were also indicated. During surgery presence of multiple cysts in the left kidney with caseous aspect, left ureter obstruction with caseous content in the lumen and bladder mucosa with friable and thickened wall were found. Histopathological study revealed chronic necrotizing granulomatous inflammation. Mantoux tuberculin skin test was strongly reactive, and family history was positive for pulmonary tuberculosis 10 years earlier. This paper shows the importance of bringing extrapulmonary tuberculosis to the roll of differential diagnosis of hematuria. Early treatment is important to avoid disease progression with functional loss of the organs as happened in this case.
ISSN:2148-2969
2148-2969
DOI:10.14534/PUCR.2016520780