We read with great interest the article by Sato et al., recently published in Pediatric Nephrology, who presented a patient with atypical Pneumocystis jiroveci pneumonia (PCP) with multiple nodular granulomas after rituximab therapy for refractory nephrotic syndrome [1]. We would like to present a case of our patient who, interestingly, revealed a different clinical course compared with that described by Sato and colleagues.
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