Pneumococcal vaccine failure: can it be a primary immunodeficiency? 2014

Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
Hospital Pediátrico de Coimbra, Centro Hospitalar e Universitário de coimbra, Coimbra, Portugal.

Vaccine failure is a rare condition and the need to investigate a primary immunodeficiency is controversial. We present the case of a 4-year-old boy, with complete antipneumococcal vaccination, who had necrotising pneumonia with pleural effusion and severe pancytopaenia with need for transfusion. A vaccine-serotype Streptococcus pneumoniae was isolated in the blood culture. On follow-up, detailed medical history, laboratory and genetic investigation led to the diagnosis of X linked dyskeratosis congenita. Dyskeratosis congenita is an inherited disorder that causes shortening or dysfunction of telomeres, affecting mainly rapidly dividing cells (particularly in the skin and haematopoietic system). It leads to bone marrow failure, combined immunodeficiency and predisposition to cancer. The confirmation of this diagnosis allows genetic counselling and medical monitoring of these patients, in order to detect early complications such as bone marrow aplasia or malignancies.

UI MeSH Term Description Entries
D007153 Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. Antibody Deficiency Syndrome,Deficiency Syndrome, Immunologic,Deficiency Syndromes, Antibody,Deficiency Syndromes, Immunologic,Immunologic Deficiency Syndrome,Immunological Deficiency Syndromes,Antibody Deficiency Syndromes,Deficiency Syndrome, Antibody,Deficiency Syndrome, Immunological,Deficiency Syndromes, Immunological,Immunological Deficiency Syndrome,Syndrome, Antibody Deficiency,Syndrome, Immunologic Deficiency,Syndrome, Immunological Deficiency,Syndromes, Antibody Deficiency,Syndromes, Immunologic Deficiency,Syndromes, Immunological Deficiency
D008297 Male Males
D010996 Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. Effusion, Pleural,Effusions, Pleural,Pleural Effusions
D011018 Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. Pneumococcal Pneumonia,Pneumococcal Pneumonias,Pneumonias, Pneumococcal
D011859 Radiography Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film). Radiology, Diagnostic X-Ray,Roentgenography,X-Ray, Diagnostic,Diagnostic X-Ray,Diagnostic X-Ray Radiology,X-Ray Radiology, Diagnostic,Diagnostic X Ray,Diagnostic X Ray Radiology,Diagnostic X-Rays,Radiology, Diagnostic X Ray,X Ray Radiology, Diagnostic,X Ray, Diagnostic,X-Rays, Diagnostic
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D013296 Streptococcus pneumoniae A gram-positive organism found in the upper respiratory tract, inflammatory exudates, and various body fluids of normal and/or diseased humans and, rarely, domestic animals. Diplococcus pneumoniae,Pneumococcus
D017211 Treatment Failure A measure of the quality of health care by assessment of unsuccessful results of management and procedures used in combating disease, in individual cases or series. Failure, Treatment,Failures, Treatment,Treatment Failures
D019871 Dyskeratosis Congenita A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. (from Int J Paediatr Dent 2000 Dec;10(4):328-34) The X-linked form is also known as Zinsser-Cole-Engman syndrome and involves the gene which encodes a highly conserved protein called dyskerin. Dyskeratosis Congenita, X-Linked,Zinsser-Cole-Engman Syndrome,Congenita, X-Linked Dyskeratosis,Dyskeratosis Congenita, X Linked,Syndrome, Zinsser-Cole-Engman,X-Linked Dyskeratosis Congenita,X-Linked Dyskeratosis Congenitas,Zinsser Cole Engman Syndrome

Related Publications

Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
January 1980, Progress in clinical and biological research,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
November 2014, Pediatrics,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
July 2014, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
January 1996, European journal of clinical pharmacology,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
May 1987, The New England journal of medicine,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
August 1986, American family physician,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
December 1981, American journal of diseases of children (1960),
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
April 2007, Journal of hepatology,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
May 2004, Inflammatory bowel diseases,
Rita Moinho, and Ana Brett, and Gisela Ferreira, and Sónia Lemos
April 2006, Vaccine,
Copied contents to your clipboard!