Skip to main content

Plastic bronchitis due to adenoviral infection: a case report



Plastic bronchitis (PB) frequently occurs as a serious postoperative complication of the Fontan procedure. The definitive causes of PB are unknown.

Case presentation

Herein, we report a pediatric case of PB secondary to adenoviral infection. A 4-year-old girl was admitted to the general pediatric ward for cough since 2 weeks and fever since 11 days. Consolidated lesions were noted in the right upper and both lower lung lobes. Extracorporeal membrane oxygenation was performed because the patient’s respiratory failure remained unalleviated despite the use of a ventilator. Bronchial dendritic casts were extracted using flexible bronchoscopy, and the patient’s breathing improved. Pathological examination of the dendritic cast confirmed the diagnosis of type I PB. The exfoliated cells of sputum and cells from bronchoalveolar lavage fluid were positive for adenoviral antigen. Human adenovirus 7 was detected by next-generation sequencing of the bronchoalveolar lavage fluid. The patient recovered and was discharged 39 days after admission without recurrence of cough or wheezing.


PB due to human adenovirus 7 infection should be considered in children with persistent respiratory failure. Flexible bronchoscopy should be performed early to confirm diagnosis and to remove any airway obstruction.

Peer Review reports


Plastic bronchitis (PB), which is characterized by the formation of endobronchial casts of undefined etiology, results in confined or extensive bronchial blockage, ventilation defects, dysfunctional gas transfer, and even life-threatening respiratory and circulatory failure [1]. Cases of PB are divided into the following two types: type I (inflammatory casts) predominantly involves fibrin with dense eosinophilic infiltration and is usually the underlying cause of inflammatory lung disease, and type II (acellular casts) predominantly involves mucin, without any acute inflammatory infiltration and occasional appearance of few mononuclear cells [2]. Pediatric cases of PB have been reported in several diseases, such as asthma, allergic diseases, cystic fibrosis, and acute chest syndrome associated with sickle-cell disease [3]. Current studies focus on Fontan treatment for the therapeutic management of complicated cases of childhood congenital heart diseases-induced PB, which is an important complication with a mortality rate of approximately 4–14% [4]. Human adenovirus 7, an important member of the human adenovirus family, a main cause of acute respiratory tract infection, especially among the Asian population, including that in our area, can cause pharyngeal conjunctival fever, acute encephalitis, and even fatal pneumonia [5]. To our knowledge, pediatric cases of PB secondary to adenovirus 7 infection have not been reported. Herein, we report the case of a child with human adenovirus 7 infection associated with fatal PB, and highlight the clinical features, diagnosis, and therapy for this rare condition.

Case presentation

A 4-year-old girl was referred to the general pediatric ward because of intractable hypoxemia, cough since 2 weeks, and fever since 11 days. Her highest body temperature was 40.6 °C. Peripheral blood cell counts were within the normal range, and etiological examination was not performed due to technical limitations. Azithromycin, ceftriaxone, cefoperazone sodium, and sulbactam sodium were previously administrated in the given order at a local hospital for infection. In the emergency department, face-mask ventilation was administered to maintain the blood oxygen saturation level over 95%. The patient is the second child of non-consanguineous parents, and with an uneventful birth and medical history. On physical examination, coarse breath sounds and wet rales were observed in both lungs. The suprasternal and supraclavicular fossa showed obvious depression.

Laboratory examinations on admission showed increased white blood cell count 21.33 × 109 cells/L (normal range, 4.0–12.0 × 109/L) with 91.4% neutrophils, hemoglobin level of 121 g/L (normal range, 110–155 g/L), platelets 258 × 1012/L (normal range, 100–400 × 109/L), hypersensitive C-reactive protein level of 44.97 mg/L (normal range, < 8 mg/L), and procalcitonin level of 25.73 ng/mL (normal range, < 0.46 ng/mL). Biochemical examination revealed reduction in albumin (normal range, 32.0–52.0 g/L), and increase in alanine aminotransferase (103 U/L, normal range, < 50 U/L) and aspartate aminotransferase levels (216 U/L, normal range, 15–60 U/L). Immunofluorescence of exfoliated cells of sputum for adenoviral, respiratory syncytial virus, influenza virus, and parainfluenza virus were weakly positive for the adenoviral antigen. RNA of Mycoplasma pneumoniae in sputum, antibodies for Mycoplasma pneumoniae and Chlamydia pneumoniae in blood, and 16S rRNA screening for gram-positive and gram-negative bacteria, and multiple blood cultures (e.g., L-form bacteria, anaerobic bacteria, fungus) were negative. The results of tests related to the tuberculosis antibody—enzyme-linked immunospot, tuberculin, (1, 3) B-D glucan, and Galactomannan were negative.

Chest radiography and computed tomography (CT) scans indicated features of consolidation and progressive worsening, especially in the right upper and both lower lung lobes. Signs of airway obstruction (e.g., finger-in-glove pattern or bronchiectasis disappearance) were not obvious. (Fig. 1a-b). Ultrasound examination showed bilateral pleural effusion of approximately 0.77 cm and 1.74 cm thickness in the left and right sides, respectively. Additionally, peritoneal (maximum depth 5.0 cm) and pelvic (maximum depth 2.1 cm) effusions were noted. Thoracentesis was performed 6 days after admission, and approximately 50 mL of slightly turbid, yellowish pleural effusion fluid was collected.

Fig. 1

Radiology findings. a Chest radiography scan shows consolidation in the right upper and both lower lung lobes; b Chest computed tomography (CT) scan shows consolidation in the right upper and both lower lung lobes; c Chest CT scan shows significant resorption of the consolidated lesions; d Chest CT scan shows an almost complete disappearance of the consolidated lesions

Although antibiotics such as sulperazone, meropenem, voriconazole, and linezolid; corticosteroids; inhaled oxygen; and additional supportive treatments such as parenteral nutrition and external cooling were administered, the patient experienced type II respiratory failure with face-mask oxygen inhalation (Fig. 2). Her white blood cell count decreased to 1.45 × 109/L with a neutrophil count of 0.87 × 109/L. Anemia (hemoglobin, 86 g/L) and thrombocytopenia (platelets, 78 × 109/L) were noted 5 days after admission. Bone marrow examination showed significant granulocyte proliferation, consistent with infection. Mechanical ventilation was adopted. However, the patient’s respiratory failure did not alleviate, and airway obstruction was speculated. Extracorporeal membrane oxygenation (ECMO) was implemented on the 7th day after admission, and flexible bronchoscopy was performed on the 8th day after admission. Flexible bronchoscopy showed complete obstruction of the right bronchiole by a white and elastic substance (Fig. 3a). Tree-like plastic casts were removed from the bronchi (Fig. 3b). Pathological examination showed flaky and cellulose-like necrotic tissue with extensive eosinophil infiltration consistent with type I PB (Fig. 3c). Immunofluorescence of bronchoalveolar lavage fluid (BALF) cells for respiratory viruses was positive for the adenoviral antigen and negative for respiratory syncytial virus, influenza virus and parainfluenza virus. Pathogen analysis of BALF was performed by next-generation sequencing (BGISEQ-50), and the data were compared with pathogen sequences deposited in the 4 Microbial Genome Databases, which included 3446 species of bacteria, 206 species of fungi, 4152 species of viruses, and 140 species of parasites. The amplified sequences showed a 99.80% match with that of the human adenovirus 7. BALF and pleural effusion cultures were negative.

Fig. 2

Diagrammatic representation of the treatment and outcome

Fig. 3

Findings of bronchoscopic and histopathological examinations. a Flexible bronchoscopy showed complete obstruction of the right bronchiole by a white and elastic substance. b A bronchial tree-like plastic dendritic cast was extracted using flexible bronchoscopy. c Hematoxylin-eosin staining of the bronchial tree-like casts shows flaky cellulose-like necrotic tissue with extensive eosinophilic infiltration (× 100)

Type II respiratory failure improved after the plastic casts were successfully removed. ECMO support lasted for 7 days, and a subsequent flexible bronchoscopy performed 15 days after admission showed no recurrence of bronchial tree-like plastic casts. Chest radiography and CT showed gradual resorption of the pulmonary consolidation (Fig. 1c), and eventually, ventilator support was removed. Nebulized inhaled corticosteroid was administered on all 39 days; methylprednisolone was administered for 11 days to inhibit systemic inflammation. Antibiotics (meropenem, voriconazole, linezolid, and cefoperazone), intravenous immunoglobulin (IVIG), red blood cells and plasma, albumin infusion, and parenteral nutrition were additionally administered (Fig. 2). The patient was discharged 39 days after admission and continued to receive nebulized inhaled hormone therapy for 7 days. During the subsequent one-year follow-up, chest CT demonstrated improvement of obstructive features (emphysema or atelectasis) (Fig. 1d), with no complaints of recurrent cough or wheezing.

Discussion and conclusion

PB is an acute and critical pediatric condition, which causes extremely severe cardiopulmonary failure. Histopathology examination of specimens from our patient revealed patchy, fibrinoid, necrotic tissue with extensive acute and chronic inflammatory cell infiltration, and eventually, a diagnosis of type I PB was rendered. Hence, in patients with irreversible respiratory failure, PB should be considered as a differential diagnosis. CT scan may yield a finger-in-glove pattern in case of widespread plugging of the central airways. In this case, there was no central airway blockage, and only suggested signs of atelectasis were observed.

Accurate epidemiological data of this rare condition are still lacking. Most cases have been reported in children with congenital cardiac defects. Recently, new etiologies of PB have been identified, such as human bocavirus, influenza virus, and adenovirus B1 infections; tumor infiltration; and lung transplantation [3, 6,7,8,9,10,11,12]. To the best of our knowledge, this is the first case of human adenovirus 7 infection-induced PB. Adenovirus-induced pneumonia is a common virus-induced pneumonia in China, characterized by acute fever, radiological features of consolidation, and ineffective outcomes with antibiotic therapy [13]. As human cells are permissive to the growth and replication of human adenoviruses, the virus replicates in the airway epithelium, inducing toxic inflammatory storm (similar to that in our case), and eventually, cell lysis and cell death. Serious cases of human adenovirus infection present with exfoliation of epithelium, infiltration of inflammatory cells and mucus in the bronchial cavity, and occlusion of the bronchial lumen (obstructive bronchitis). This may have been the risk factor for PB in our case. Moreover, direct infection, inflammatory storm, hypoxemia, and carbon dioxide retention may impair the functions of other important organs (e.g., liver) [14]. Hence, human adenovirus 7 should be investigated as a causative pathogen in patients with PB.

The clinical manifestations of PB are diverse; the main features include cough, chest pain, wheezing, shortness of breath, severe respiratory distress, severe systemic hypoxia, and death due to cardiopulmonary failure and multiple organ dysfunction [15]. Besides cough, persistent high fever, damage to liver functions, and multi-serous cavity effusion were observed in our patient with type II respiratory failure, which remained unalleviated despite ventilator support and necessitated ECMO support.

The gold standard for the diagnosis of PB is the detection of bronchial dendritic casts with flexible bronchoscopy [16]. To date, there is no effective anti-adenovirus treatment. IVIG and corticosteroids were suggested for severe adenovirus pneumonia. Removal of the airway-occluding plastic casts using flexible bronchoscopy and bronchoalveolar lavage was most vital for treating PB [17]. Recently, other treatments of PB have mainly focused on percutaneous thoracic intervention after the Fontan procedure, including the administration of low-dose azithromycin, inhaled bronchodilators, and use of recombinant human DNase [18,19,20]. In addition, nebulization with N-acetylcysteine and biphasic cuirass ventilation have also been reported [21]. Similarly, in our case, hypoxemia was resolved after removal of the plastic casts. ECMO aided patient recovery during the critical period of respiratory failure, and therefore, may be a good method of life support before removal of plastic casts in patients with PB and in similar situations [22].

In conclusion, PB due to human adenovirus 7 infection should be considered as a differential diagnosis in children with unalleviated respiratory failure. Flexible bronchoscopy should be performed early to confirm the diagnosis of PB and to clear airway obstructions. Although the disease progresses rapidly, the prognosis of PB caused by human adenovirus 7 infection was satisfactory with timely and effective treatment.

Availability of data and materials

The datasets generated and/or analyzed during the current study are available.



Bronchoalveolar lavage fluid


Extracorporeal membrane oxygenation


Intravenous immunoglobulin


Next-generation sequencing


Plastic bronchitis


  1. 1.

    Hasan RA, Black C, Reddy R. Plastic bronchitis in children. Fetal Pediatr Pathol. 2012;31:87–93.

    Article  Google Scholar 

  2. 2.

    Seear M, Hui H, Magee F, et al. Bronchial casts in children: a proposed classification based on nine cases and a review of the literature. Am J Respir Crit Care Med. 1997;155:364–70.

    CAS  Article  Google Scholar 

  3. 3.

    Raghuram N, Pettignano R, Gal AA, et al. Plastic bronchitis: an unusual complication associated with sickle cell disease and the acute chest syndrome. Pediatrics. 1997;100:139–42.

    CAS  Article  Google Scholar 

  4. 4.

    Caruthers RL, Kempa M, Loo A, et al. Demographic characteristics and estimated prevalence of Fontan-associated plastic bronchitis. Pediatr Cardiol. 2013;34:256–61.

    Article  Google Scholar 

  5. 5.

    Murtagh P, Giubergia V, Viale D, et al. Lower respiratory infections by adenovirus in children. Clinical features and risk factors for bronchiolitis obliterans and mortality. Pediatr Pulmonol. 2009;44:450–6.

    Article  Google Scholar 

  6. 6.

    Hasegawa M, Inamo Y, Fuchigami T, et al. Bronchial casts and pandemic (H1N1) 2009 virus infection. Emerg Infect Dis. 2010;16:344–6.

    Article  Google Scholar 

  7. 7.

    Jikui D, Yuejie Z, Chengrong L, et al. Plastic bronchitis in three children associated with 2009 influenza a(H1N1) virus infection. Chest. 2010;138:1486–8.

    Article  Google Scholar 

  8. 8.

    Kim S, Cho HJ, Han DK, et al. Recurrent plastic bronchitis in a child with 2009 influenza a (H1N1) and influenza B virus infection. J Korean Med Sci. 2012;27:1114–9.

    Article  Google Scholar 

  9. 9.

    Lu Z, Zheng Y. Plastic bronchitis associated with adenovirus infection. Lancet Infect Dis. 2018;18:474.

    Article  Google Scholar 

  10. 10.

    Oikawa J, Ogita J, Ishiwada N, et al. Human Bocavirus DNA detected in a boy with plastic bronchitis. Pediatr Infect Dis J. 2009;28:1035–6.

    Article  Google Scholar 

  11. 11.

    Kuperman T, Wexler ID, Shoseyov D, et al. Plastic bronchitis caused by neoplastic infiltrates in a child. Pediatr Pulmonol. 2006;41:893–6.

    Article  Google Scholar 

  12. 12.

    Michael E, Kalpaj P, Sif H, et al. Plastic bronchitis complicating primary graft dysfunction after lung transplantation. Ann Thorac Surg. 2014;98:1849.

    Article  Google Scholar 

  13. 13.

    Gupta P, Tobias JD, Goyal S, et al. Prolonged mechanical support in children with severe adenoviral infections: a case series and review of the literature. J Intensive Care Med. 2011;26:267–72.

    Article  Google Scholar 

  14. 14.

    Lai CY, Lee CJ, Lu CY, et al. Adenovirus serotype 3 and 7 infection with acute respiratory failure in children in Taiwan, 2010-2011. PLoS One. 2013;8:e53614.

    CAS  Article  Google Scholar 

  15. 15.

    Tin J, Kozak FK, Moxham JP, et al. Casting a look at pediatric plastic bronchitis. Int J Pediatr Otorhinolaryngol. 2015;79:1658–61.

    Article  Google Scholar 

  16. 16.

    Preciado D, Verghese S, Choi S. Aggressive bronchoscopic management of plastic bronchitis. Int J Pediatr Otorhinolaryngol. 2010;74:820–2.

    Article  Google Scholar 

  17. 17.

    Soyer T, Yalcin Ş, Emiralioğlu N, et al. Use of serial rigid bronchoscopy in the treatment of plastic bronchitis in children. J Pediatr Surg. 2016;51:1640–3.

    Article  Google Scholar 

  18. 18.

    Schultz KD, Oermann CM. Treatment of cast bronchitis with low-dose oral azithromycin. Pediatr Pulmonol. 2003;35:139–43.

    Article  Google Scholar 

  19. 19.

    Manna SS, Shaw J, Tibby SM, et al. Treatment of plastic bronchitis in acute chest syndrome of sickle cell disease with intratracheal rhDNase. Arch Dis Child. 2003;88:626.

    CAS  Article  Google Scholar 

  20. 20.

    DePopas EM, Veress LA, Ahmed F, et al. Percutaneous thoracic duct intervention to treat plastic bronchitis related to Fontan palliation. Pediatr Pulmonol. 2017;52:E97–E101.

    Article  Google Scholar 

  21. 21.

    Okada S, Muneuchi J, Nagatomo Y, et al. Successful treatment of protein-losing Enteropathy and plastic bronchitis by biphasic cuirass ventilation in a patient with failing Fontan circulation. Int Heart J. 2018;59:873–6.

    Article  Google Scholar 

  22. 22.

    Millar JE, Bartnikowski N, von Bahr V, et al. Extracorporeal membrane oxygenation (ECMO) and the acute respiratory distress syndrome (ARDS): a systematic review of pre-clinical models. Intensive Care Med Exp. 2019;7:18.

    Article  Google Scholar 

Download references


We thank the patient and his parents for permitting us to use the data and and the National Natural Science Foundation (81170016 & 81470214) and Zhejiang Provincial Program for the Cultivation of High-Level Innovative Health Talents.


This work was supported by the National Natural Science Foundation (81170016 & 81470214) and the Zhejiang Provincial Program for the Cultivation of High-Level Innovative Health Talents. The funding provided support for the cost of next-generation sequencing and publication for the patient.

Author information




LFT conceptualized and designed the study, and reviewed and revised the manuscript. FZZ drafted the initial manuscript. LQ collected data. JXY was responsible for the follow-up. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

Corresponding author

Correspondence to Lan Fang Tang.

Ethics declarations

Ethics approval and consent to participate

The Ethics Committee of Zhejiang University Medical College has agreed to the retrospective case report, arguing that there is no ethical dispute in the study.

Consent for publication

Written informed consent for publication was obtained from the parent of the child described in this case report.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhang, F.Z., Qin, L., Yuan, J.X. et al. Plastic bronchitis due to adenoviral infection: a case report. BMC Pediatr 20, 61 (2020).

Download citation


  • Plastic bronchitis
  • Human adenovirus 7
  • Bronchoscopy
  • Extracorporeal membrane oxygenation