Volume 19, Issue 5 pp. E115-E120
Case Report

Fatal rituximab-associated lung injury syndrome in a patient treated with rituximab for recurrence of post-transplant nephrotic syndrome

Ryszard Grenda

Corresponding Author

Ryszard Grenda

Department of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, Warsaw, Poland

Ryszard Grenda, MD, PhD, Oddział Nefrologii, Transplantacji Nerek i Nadciśnienia Tętniczego (Department of Nephrology, Kidney Transplantation and Hypertension), Instytut Pomnik – Centrum Zdrowia Dziecka, Aleja Dzieci Polskich 20, 04-730 Warszawa, Polska

Tel.: +48228157449

Fax: +48228151541

E-mail: [email protected]

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Wioletta Jarmużek

Wioletta Jarmużek

Department of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, Warsaw, Poland

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Jacek Rubik

Jacek Rubik

Department of Nephrology, Kidney Transplantation and Hypertension, The Children's Memorial Health Institute, Warsaw, Poland

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Marek Migdał

Marek Migdał

Intensive Care Unit, Department of Anesthesiology and Intensive Care, The Children's Memorial Health Institute, Warsaw, Poland

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Maciej Pronicki

Maciej Pronicki

Department of Pathology, The Children's Memorial Health Institute, Warsaw, Poland

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First published: 30 April 2015
Citations: 10

Abstract

Rituximab (anti-B CD20 ab.) in recently widely used in renal transplantation. Case history: A 10-yr-old patient with end-stage renal failure due to multidrug-resistant NS was transplanted with renal graft from deceased donor and presented immediate recurrence of NS. PF was started on day 3 and patient received MP pulses, however with no effect. Rituximab (4 × 375 mg/m2) was administered. Chest radiographs taken at that time were normal. Partial remission was achieved and the patient was discharged in good condition. Sequential recurrence appeared two wk afterward. Twelve sessions of PF were performed and six pulses of MP were given, effecting a partial remission. Three months after the last dose of rituximab, patient was admitted with increasing respiratory failure, requiring mechanical ventilation. Infectious background, including CMV, BKV, mycoplasma, and pneumocystis, was not confirmed. The patient was treated with MP pulses, IVIG, and a variety of antibiotics. Ground-glass opacity was confirmed on lung CT images. Respiratory failure worsened, despite aggressive ventilation and patient passed away after three wk at ICU. A destruction of alveolar epithelium and extended pulmonary fibrosis was confirmed in the autopsy report. The case represents a fatal RALI.

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