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Disseminated BCG Disease in an Infant with Severe Combined Immunodeficiency | OMICS International| Abstract
2476-213X

Journal of Clinical Infectious Diseases & Practice
Open Access

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  • Case Report   
  • J Clin Infect Dis Pract 2016, Vol 1(2): 112
  • DOI: 10.4172/2476-213X.1000112

Disseminated BCG Disease in an Infant with Severe Combined Immunodeficiency

Anirban Mandal1*, Amitabh Singh2, Puneet Kaur Sahi3 and Bhavika Rishi4
1Department of Pediatrics, Sitaram Bhartia Institute of Science and Research, New Delhi, , India
2Department of Pediatrics, Chacha Nehru Bal Chikitsalaya, , New Delhi, India
3Department of Pediatrics, Kalawati Saran Children’s Hospital, New Delhi, , India
4Department of Pathology, Lady Harding Medical College, New Delhi, , India
*Corresponding Author : Anirban Mandal, Attending Consultant, Department of Pediatrics, Sitaram Bhartia Institute Of Science And Research, New Delhi, India, Tel: 8826836670, Email: anirban.nrs@gmail.com

Received Date: Oct 06, 2016 / Accepted Date: Oct 21, 2016 / Published Date: Oct 24, 2016

Abstract

BCG (Bacillus Calmette Guerin) being a live attenuated vaccine may cause disseminated disease (BCGiosis) in patients with impaired immunity. Patients with severe combined immunodeficiency (SCID) having defect in both cellular and humoral immunity are predisposed to a host of live vaccine related complications, especially BCG.

We report a 6 month-old baby boy with fever for 5 months, generalized rash for 3 months, cough and cold for 1 month, poor feeding and weight loss over last 1 month. He had an uneventful perinatal period and received BCG at birth. Examination revealed mild pallor, generalized erythematous papular rash with central crusting and splenohepatomegaly. Skin biopsy and culture confirmed BCG infection while computed tomography of abdomen and skeletal survey showed disseminated involvement. Immunological investigations were suggestive of an underlying SCID. The infant showed improvement with antitubercular therapy combined with intravenous immunoglobulin and other supportive measures.

The case highlights the possible risk of such rare yet lethal complication of BCG especially at places where it is given routinely at birth or in the neonatal period and also emphasizes the need for neonatal screening for SCID in such regions.

Keywords: Primary immunodeficiency; Adverse event following immunization; Hematopoietic stem cell transplantation; Neonatal screening

Citation: Mandal A, Singh A, Sahi PK, Rishi B (2016) Disseminated BCG Disease in an Infant with Severe Combined Immunodeficiency. J Clin Infect Dis Pract 1:112. Doi: 10.4172/2476-213X.1000112

Copyright: © 2016 Mandal A et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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