Rituximab-induced pneumonitis mimicking miliary tuberculosis

Abstract

Rituximab, a chimeric anti-CD20 monoclonal antibody, is commonly being used in combination with chemotherapy regimens in the standard treatment of B-cell non-Hodgkin lymphoma (NHL) [1]. Rituximab is considered to be a relatively safe drug but recently, severe and fatal interstitial lung disease (ILD) was noted with an occurrence rate of 0.01-0.03% [2]. Computed tomography (CT) patterns of rituximabinduced ILD include focal (54%) or diffused (9%) alveolar patterns and macronodules (3%), or groundglass patterns (34%) [2]. In this regard, we report a patient with NHL in whom ILD developed after six cycles of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone) therapy with diffused micronodules mimicking miliary tuberculosis (TB). R-CHOP was discontinued and the patient gradually recovered.This 54-year-old housewife, who initially presented with abdominal fullness due to intra-abdominal lymphadenopathy, was diagnosed with diffused large B-cell lymphoma. She was treated with R-CHOP three times a week. Several days after the sixth cycle of treatment she reported dyspnoea, fever and cough. Physical examination was unremarkable. Pulse oximetry and analysis of arterial blood gases confirmed the presence of hypoxaemia. A chest radiography and CT scan ( fig. 1) showed bilateral diffuse micronodules. Bone marrow biopsy revealed no granuloma or malignancy, and acid-fast stains and culture for mycobacteria were negative. The patient underwent bronchoscopy with bronchoalveolar lavage and transbronchial biopsies. Culture for bacteria, fungi and mycobacteria were all negative. PCR did not detect any Pneumocystis jiroveci DNA. The transbronchial biopsy revealed interstitial fibrosis and type II pneumocyte hyperplasia ( fig. 2). No granuloma or malignancy was observed. We prescribed supportive treatment without specific medications (including steroids) and her symptoms improved. 4 months later, CT of the chest also revealed marked improvement and she was asymptomatic.The common differential diagnosis of randomly distributed micronodules on CT patterns includes miliary TB, miliary fungus and haematogenous metastasis [3]. Because the patient lived in a TB-endemic region and was in an immunocompromised state, we took miliary TB as the first consideration. The final diagnosis of rituximab-induced ILD was mainly made based on the lack of pathological or microbial infection evidence and the dramatic improvement in the patient's condition after the discontinuation of R-CHOP.The time to onset of rituximab-induced ILD is usually classified as early (day 1), delayed (days 7-21) or late (.30 days). Mechanisms leading to late-onset ILD remain unclear. A potential explanation may be the induction and release of cytokines following rituximab binding to CD20 + cells [2,4]. Because the patient was treated concomitantly with cytotoxic drugs, we recognise that it is difficult to completely rule out cytotoxic FIGURE 1 Chest computed tomography scan revealing diffused micronodules over bilateral lung field. LETTER 587 drug-i...

Drug-Related Pneumonitis During Mammalian Target of Rapamycin Inhibitor Therapy: Radiographic Pattern-Based Approach in Waldenström Macroglobulinemia as a Paradigm

“…In the present study, 70% of the patients received rituximab with or without bortezomib, which might have contributed to the higher frequency because both agents have been reported to be associated with pneumonitis in some previous reports [7,[17][18][19][20][21][22]. Also, rituximab has recently been used to treat interstitial lung diseases [23,24].…”