• Users Online: 26
  • Print this page
  • Email this page


 
 Table of Contents  
LETTER TO EDITOR
Year : 2021  |  Volume : 10  |  Issue : 3  |  Page : 368-369

Granulomatosis with polyangiitis and dengue fever: A rare association


1 Department of Respiratory Medicine, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, Uttar Pradesh, India
2 Department of Psychiatry, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, Uttar Pradesh, India

Date of Submission05-Jun-2021
Date of Decision17-Jul-2021
Date of Acceptance21-Jul-2021
Date of Web Publication13-Sep-2021

Correspondence Address:
Dr. Manoj Pandey
Assistant Professor, Department of Respiratory Medicine, GSVM Medical College, Kanpur, Uttar Pradesh
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijrc.ijrc_68_21

Rights and Permissions

How to cite this article:
Pandey A, Pandey M, Kumar H, Natasha. Granulomatosis with polyangiitis and dengue fever: A rare association. Indian J Respir Care 2021;10:368-9

How to cite this URL:
Pandey A, Pandey M, Kumar H, Natasha. Granulomatosis with polyangiitis and dengue fever: A rare association. Indian J Respir Care [serial online] 2021 [cited 2021 Dec 2];10:368-9. Available from: http://www.ijrc.in/text.asp?2021/10/3/368/325887



Sir,

A 45-year-old female presented to us with the complaint of bleeding gums, rashes, and fever from the past 20 days. She also had dyspnea on exertion and mild nonproductive cough from the past 1 week. On further inquiry, she had red discoloration of urine and stool. There was no history of diabetes, hypertension, or tuberculosis. On examination, the patient had hemorrhagic spots over the buccal mucosa and petechial rashes all over the body. Other examination findings were within the normal limits. With the above complaint, a differential diagnosis of novel coronavirus disease 2019 along with viral hemorrhagic fever, idiopathic thrombocytopenic purpura, aplastic anemia, and hematological malignancy was kept in consideration. The patient was kept on empirical broad-spectrum antibiotics along with other supportive treatments. On further investigation her platelet count was-38,000/ml which when repeated further reduced to <10,000/ml. Serum urea was 34 mg/dl and serum creatinine was 0.60 mg/dl. immunoglobulin M, immunoglobulin G, and NS1 Ag for dengue were positive. Urine examination revealed the presence of blood with red blood cell count of 30–35/HPF. Stool examination for occult blood was also positive. Reverse transcription-polymerase chain reaction of her nasopharyngeal swab for COVID-19 was negative. As the patient had complaint of nonproductive cough and exertional dyspnea, a Chest X-ray was done which showed the presence of nonhomogeneous opacity in the bilateral middle and lower zones [Figure 1]. In view of chest X-ray findings high-resolution computed tomography of the thorax was advised which showed the presence of bilateral upper, middle and lower lobe infiltrates with ground-glass opacities [Figure 2]. Sputum for gram stain, acid-fast bacilli, and aerobic culture and sensitivity were negative. In view of computed tomography findings, a possibility of diffuse alveolar hemorrhage was suspected and based on that bronchoscopy was performed which revealed increase in hemorrhagic fluid on sequential Bronchoalveolar lavage when collected from the right middle lobe [Figure 3]. The platelet count of the patient just before bronchoscopy was 75,000/ml. The ANCA profile was positive with C-ANCA titer of 1:640.
Figure 1: Chest X-ray showing presence of nonhomogenous opacity in the bilateral middle and lower zones

Click here to view
Figure 2: High-resolution computed tomography thorax showing presence of bilateral upper, middle and lower lobe infiltrates with ground glass opacities

Click here to view
Figure 3: Increase in hemorrhagic fluid on sequential bronchoalveolar lavage when collected from the right middle lobe

Click here to view


Based on the above findings, the diagnosis of Granulomatosis with Polyangiitis (GPA) and Dengue fever was made. The patient showed response within 2 weeks of starting steroids and immunosuppressive therapy.

GPA is an ANCA-associated necrotizing vasculitis predominantly affecting small-sized arteries.[1] The upper and lower respiratory tract along with kidneys are most commonly and severely affected organs. Its prevalence ranges from 2.3 to 146 cases per million with the incidence of 0.4–11.9 cases per million person per year. Most commonly, it presents in older adults but cases have been reported in all age groups.[2] The cause for the development of GPA is not known but few studies have shown a higher prevalence of antibodies against Epstein–Barr virus and cytomegalovirus in patients with GPA.[3] Its association with respiratory syncytial virus infection have also been given in some studies.[4]

In our case, the patient initially had Dengue fever which is a Flavi viral infection commonly prevalent in India. During dengue infection, there is the increase in the levels of cytokines and chemokines in the blood which activates the complement system and immune cells. The anti NS-1 antibody produced during dengue infection are partially responsible for its reactivity with endothelial cells.[5]

To our knowledge, till now only one study conducted by Ghosh et al.[6] has shown the association of GPA with dengue fever. It may be hypothesized that dengue infection could have precipitated GPA in an otherwise rare category of the population. As there is overlap in the clinical manifestation of COVID-19 and dengue fever, the possibility of COVID infection should always be kept into consideration.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Jennette JC, Falk RJ, Bacon PA, Basu N, Cid MC, Ferrario F, et al. 2012 revised international chapel hill consensus conference nomenclature of vasculitides. Arthritis Rheum 2013;65:1-11.  Back to cited text no. 1
    
2.
Kitching AR, Anders HJ, Basu N, Brouwer E, Gordon J, Jayne DR, et al. ANCA-associated vasculitis. Nat Rev Dis Primers 2020;6:71.  Back to cited text no. 2
    
3.
Lidar M, Lipschitz N, Langevitz P, Barzilai O, Ram M, Porat-Katz BS, et al. Infectious serologies and autoantibodies in Wegener's granulomatosis and other vasculitides: Novel associations disclosed using the Rad BioPlex 2200. Ann N Y Acad Sci 2009;1173:649-57.  Back to cited text no. 3
    
4.
Multz AS, Keil K, Karpel JP. Respiratory syncytial virus infection in an adult with Wegener's granulomatosis. Chest 1992;101:1717-8.  Back to cited text no. 4
    
5.
Lin CF, Lei HY, Liu CC, Liu HS, Yeh TM, Chen SH et al. Autoimmunity in dengue virus infection.. WHO Regional Office for South-East Asia. Dengue Bull 2004 Dec; 28: 51-57.  Back to cited text no. 5
    
6.
Ghosh A, Banerjee A, Saha S, Pande A, Ghosh B. Wegener's granulomatosis with dengue fever: An unusual association. Int J Rheum Dis 2012;15:e47-9.  Back to cited text no. 6
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
References
Article Figures

 Article Access Statistics
    Viewed238    
    Printed0    
    Emailed0    
    PDF Downloaded9    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]