Colonic malakoplakia in a pediatric renal transplant recipient case report

Author:

Valencia Deray Kristen G1ORCID,Kellermayer Richard2,Gomez Alexis C3,Patel Kalyani R4,Imani Peace5,Kitagawa Seiji2,Bocchini Claire E1,Orjuela Alvaro5

Affiliation:

1. Division of Infectious Diseases, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA

2. Division of Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA

3. Division of Pediatric Nephrology, Department of Pediatrics, Boston Children’s Hospital, Boston, MA, USA

4. Department of Pathology & Immunology, Baylor College of Medicine, Houston, TX, USA

5. Division of Pediatric Nephrology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA

Abstract

Malakoplakia is a rare, chronic granulomatous disease that mainly affects the genitourinary system of immunocompromised adults. It is caused by a bactericidal deficit in macrophages and, therefore, the treatment includes antimicrobials that reach high concentrations in macrophages. To our knowledge, we present the first case of malakoplakia in a pediatric solid organ transplant recipient. Our patient is a 15-year-old male renal transplant recipient who presented with recurrent diarrhea. Blood, urine, and gastrointestinal pathogen panel testing were positive for enteroaggregative Escherichia coli. A colonoscopy revealed diffuse malakoplakia. He had a complete resolution of symptoms with trimethoprim-sulfamethoxazole therapy. Unfortunately, his malakoplakia recurred after 9 months prompting the transition of therapy to oral gentamicin with subsequent remission. Malakoplakia should be considered in the differential of solid organ transplant recipients with recurrent gastrointestinal infections.

Publisher

SAGE Publications

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