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1.
Arch Pediatr ; 24(5S): 5S14-5S17, 2017 May.
Artigo em Francês | MEDLINE | ID: mdl-28622776

RESUMO

Iron is essential for proper functioning of the host immune system as well as an essential nutrient for growth of various pathogens. Iron deficiency increases infection susceptibility, specially those due to intracellular pathogens. At the opposite, excess iron stores could increase the virulence of some pathogens. Hepcidin synthesis is increased during the acute inflammation phase; leading to decreased iron intestinal absorption and retention of the metal within macrophages. This is considered to result from a defense mechanism of the child to limit the availability of iron for extracellular pathogens. On the other hand, iron affect innate immune responses by influencing IFN-γ or NF-kB pathways in macrophages. Consequently, iron enhances host resistance to intracellular pathogens but excess iron may alter immune system.


Assuntos
Deficiências de Ferro , Infecções Oportunistas/etiologia , Animais , Suscetibilidade a Doenças , Humanos , Imunidade Inata , Ferro da Dieta/administração & dosagem , Infecções Oportunistas/prevenção & controle
2.
Arch Pediatr ; 24(5): 471-475, 2017 May.
Artigo em Francês | MEDLINE | ID: mdl-28365190

RESUMO

Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis, is a rare cause of lymphadenopathy in children. This benign disease can mimic lymphoma and misleads doctors. It was first described in Asia, where it occurred especially in young women. Recent publications show that it can also affect teenagers and young adults in Caucasian populations. The pathophysiology remains unknown. Three hypotheses have been raised for this disease: the role of viruses (in particular HHV-8), genetic predisposition (two alleles in HLA class II genes were found more frequently in patients with Kikuchi disease), and an autoimmune cause because of the correlation with lupus erythematosus. Few cases have been reported in Europe so far. In this article, we report three cases of Kikuchi disease observed in less than 2 months in a single hospital in France. All three patients were teenagers who presented with lymphadenopathy, either isolated or combined with fever, weakness, and weight loss. In all of them, the hypermetabolic activity of the lymph node on the PET scanner misled us to suspect lymphoma. The diagnosis of Kikuchi disease was finally made, for all patients, after 2 weeks in the hospital based on lymph node biopsy. Based on this report, we highlight that early biopsy in presence of lymphadenopathy can avoid unnecessary extensive investigations. Moreover, in this rare disease, it is very surprising to come across three cases that are not family-related, in such a short period of time. This strengthens the hypothesis of the possible implication of an environmental factor in the pathophysiology of Kikuchi disease.


Assuntos
Linfadenite Histiocítica Necrosante/diagnóstico , Linfoma/diagnóstico , Adolescente , Biópsia , Diagnóstico Diferencial , Feminino , Fluordesoxiglucose F18 , Linfadenite Histiocítica Necrosante/patologia , Humanos , Linfonodos/patologia , Linfadenopatia/etiologia , Linfadenopatia/patologia , Linfoma/patologia , Masculino , Tomografia por Emissão de Pósitrons
3.
Arch Pediatr ; 18(11): 1234-46, 2011 Nov.
Artigo em Francês | MEDLINE | ID: mdl-22019286

RESUMO

The annual meeting of the Infectious Disease Society of America (IDSA) ; which brought together nearly 5000 participants from over 80 countries in Vancouver, Canada, October 21 to 24, 2010 ; provided a review of the influenza (H1N1) 2009 pandemic, evaluated vaccination programmes and presented new vaccines under development. With 12,500 deaths in the United States in 2009-2010, the influenza (H1N1) 2009 pandemic was actually less deadly than the seasonal flu. But it essentially hit the young, and the toll calculated in years of life lost is high. The monovalent vaccines, whether live attenuated or inactivated with or without adjuvants, were well tolerated in toddlers, children, adults and pregnant women. In order to protect infants against pertussis, family members are urged to get their booster shots. The introduction of the 13-valent Pneumococcal conjugated vaccine in the beginning of 2010 may solve - but for how long ? - the problem of serotype replacement, responsible for the re-increasing incidence of invasive Pneumococcal infections observed in countries that had introduced the 7-valent vaccine. The efficacy of a rotavirus vaccine has been confirmed, with a reduction in hospitalization in the United States and a reduction in gastroenteritis-related deaths in Mexico. In the United States, vaccination of pre-adolescents against human papillomavirus (HPV) has not resulted in any specific undesirable effects. Routine vaccination against chicken pox, recommended since 1995, has not had an impact on the evolution of the incidence of shingles. Vaccination against shingles, recommended in the United States for subjects 60 years and over, shows an effectiveness of 55 %, according to a cohort study (Kaiser Permanente, Southern California). Although some propose the development of personalized vaccines according to individual genetic characteristics, the priority remains with increasing vaccine coverage, not only in infants but also in adults and the elderly. Vaccine calendars that cover a whole lifetime should be promoted, since the vaccination of adults and seniors is a determining factor of good health at all ages.


Assuntos
Influenza Humana/prevenção & controle , Vacinação/estatística & dados numéricos , Vacinação/normas , Vacinas , Adolescente , Criança , Pré-Escolar , Humanos , Esquemas de Imunização , Lactente , Recém-Nascido , Vacinas contra Influenza/imunologia , Influenza Humana/epidemiologia , Pandemias , Estados Unidos , Vacinas Virais
4.
Med Mal Infect ; 41(5): 278-90, 2011 May.
Artigo em Francês | MEDLINE | ID: mdl-21489733

RESUMO

The annual meeting of the Infectious Disease Society of America (IDSA); which brought together nearly 5000 participants from over 80 countries in Vancouver, Canada, October 21 to 24, 2010; provided a review of the influenza (H1N1) 2009 pandemic, evaluated vaccination programmes and presented new vaccines under development. With 12,500 deaths in the United States in 2009-2010, the influenza (H1N1) 2009 pandemic was actually less deadly than the seasonal flu. But it essentially hit the young, and the toll calculated in years of life lost is high. The monovalent vaccines, whether live attenuated or inactivated with or without adjuvants, were well tolerated in toddlers, children, adults and pregnant women. In order to protect infants against pertussis, family members are urged to get their booster shots. The introduction of the 13-valent Pneumococcal conjugated vaccine in the beginning of 2010 may solve--but for how long?--the problem of serotype replacement, responsible for the re-increasing incidence of invasive Pneumococcal infections observed in countries that had introduced the 7-valent vaccine. The efficacy of a rotavirus vaccine has been confirmed, with a reduction in hospitalization in the United States and a reduction in gastroenteritis-related deaths in Mexico. In the United States, vaccination of pre-adolescents against human papillomavirus (HPV) has not resulted in any specific undesirable effects. Routine vaccination against chicken pox, recommended since 1995, has not had an impact on the evolution of the incidence of shingles. Vaccination against shingles, recommended in the United States for subjects 60 years and over, shows an effectiveness of 55%, according to a cohort study (Kaiser Permanente, Southern California). Although some propose the development of personalized vaccines according to individual genetic characteristics, the priority remains with increasing vaccine coverage, not only in infants but also in adults and the elderly. Vaccine calendars that cover a whole lifetime should be promoted, since the vaccination of adults and seniors is a determining factor of good health at all ages.


Assuntos
Vacinação , Congressos como Assunto , Humanos
5.
Arch Pediatr ; 17(8): 1220-7, 2010 Aug.
Artigo em Francês | MEDLINE | ID: mdl-20598868

RESUMO

Biology, genetics and environment of childhood solid tumours set them apart from adult solid tumours. The nature of the progenitor cells from which these tumours arise, and their immature tissue environment, allows childhood solid tumours to develop with fewer defects in cell regulatory processes. Constitutional molecular defects are known to play a role in childhood solid tumours, as shown by the increased incidence of embryonic cancers in children carrying malformations associated with childhood cancer. These rare diagnoses are commonly missed. In this article, we reviewed the spectrum of these tumour predisposition syndromes.


Assuntos
Aberrações Cromossômicas/classificação , Neoplasias/etiologia , Adulto , Criança , Predisposição Genética para Doença , Humanos , Incidência , Neoplasias/embriologia , Neoplasias/epidemiologia , Neoplasias/genética
6.
Hum Mutat ; 28(8): 790-6, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17397038

RESUMO

Hirschsprung disease (HSCR) stands as a model for genetic dissection of complex diseases. In this model, a major gene, RET, is involved in most if not all cases of isolated (i.e., nonsyndromic) HSCR, in conjunction with other autosomal susceptibility loci under a multiplicative model. HSCR susceptibility alleles can harbor either heterozygous coding sequence mutations or, more frequently, a polymorphism within intron 1, leading to a hypomorphic RET allele. On the other hand, about 30% of HSCR are syndromic. Hitherto, the disease causing gene has been identified for eight Mendelian syndromes with HSCR: congenital central hypoventilation (CCHS), Mowat-Wilson (MWS), Bardet-Biedl (BBS), Shah-Waardenburg (WS4), cartilage-hair-hypoplasia (CHH), Smith-Lemli-Opitz (SLO), Goldberg-Sprintzsen (GSS), and hydrocephalus due to congenital stenosis of the aqueduct of sylvius (HSAS). According to the HSCR syndrome, the penetrance of HSCR trait varies from 5 to 70%. Trisomy 21 (T21) also predisposes to HSCR. We were able to collect a series of 393 patients affected by CCHS (n = 173), WS4 (n = 24), BBS (n = 51), MWS (n = 71), T21 (n = 46), and mental retardation (MR) with HSCR (n = 28). For each syndrome, we studied the RET locus in two subgroups of patients; i.e., with or without HSCR. We genotyped the RET locus in 393 patients among whom 195 had HSCR, and compared the distribution of alleles and genotypes within the two groups for each syndrome. RET acts as a modifier gene for the HSCR phenotype in patients with CCHS, BBS, and Down syndrome, but not in patients with MWS and WS4. The frequent, low penetrant, predisposing allele of the RET gene can be regarded as a risk factor for the HSCR phenotype in CCHS, BBS, and Down syndrome, while its role is not significant in MWS and WS4. These data highlight the pivotal role of the RET gene in both isolated and syndromic HSCR.


Assuntos
Alelos , Epistasia Genética , Doença de Hirschsprung/genética , Proteínas Proto-Oncogênicas c-ret/genética , Feminino , Frequência do Gene , Genótipo , Humanos , Masculino , Penetrância , Síndrome
7.
J Med Genet ; 43(5): 419-23, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16443855

RESUMO

BACKGROUND: In Hirschsprung's disease (HSCR), a hypomorphic allele of a major gene, RET, accounts for most isolated (non-syndromic) cases, along with other autosomal susceptibility loci under a multiplicative model. However, some syndromic forms of HSCR are monogenic entities, for which the disease causing gene is known. OBJECTIVE: To determine whether RET could be considered a modifier gene for the enteric phenotype on the background of a monogenic trait. METHODS: The syndromic HSCR entities studied were congenital central hypoventilation (CCHS) and Mowat-Wilson syndrome (MWS), caused by PHOX2B and ZFHX1B gene mutations, respectively. The RET locus was genotyped in 143 CCHS patients, among whom 44 had HSCR, and in 30 MWS patients, among whom 20 had HSCR. The distribution of alleles, genotypes, and haplotypes was compared within the different groups. To test the interaction in vivo, heterozygous mice were bred for a null allele of Phox2b and Ret genes. RESULTS: RET was shown to act as a modifier gene for the HSCR phenotype in patients with CCHS but not with MWS. The intestine of double heterozygote mice was indistinguishable from their littermates. A loss of over 50% of each gene function seemed necessary in the mouse model for an enteric phenotype to occur. CONCLUSIONS: In CCHS patients, the weak predisposing haplotype of the RET gene can be regarded as a quantitative trait, being a risk factor for the HSCR phenotype, while in MWS, for which the HSCR penetrance is high, the role of the RET predisposing haplotype is not significant. It seems likely that there are both RET dependent and RET independent HSCR cases.


Assuntos
Alelos , Doença de Hirschsprung/genética , Mutação , Proteínas Proto-Oncogênicas c-ret/genética , Animais , Mapeamento Cromossômico , Análise Mutacional de DNA , Feminino , Frequência do Gene , Haplótipos , Doença de Hirschsprung/diagnóstico , Proteínas de Homeodomínio/genética , Humanos , Masculino , Camundongos , Linhagem , Fenótipo , Polimorfismo de Nucleotídeo Único , Síndrome , Fatores de Transcrição/genética
8.
Med Mal Infect ; 35(3): 170-2, 2005 Mar.
Artigo em Francês | MEDLINE | ID: mdl-15878818

RESUMO

Many Mycoplasma pneumoniae extra respiratory infections have already been reported. The authors report the case of an eight year old child, presenting with acute transverse myelitis, with a PCR proven involvement of M. pneumoniae in CSF as well as the presence of specific IgM in blood. Acute transverse myelitis may have many causes, most of the time viral. The mechanisms of neurological involvement in M. pneumoniae infections are still unclear, but several points indicate an immune reaction. Corticotherapy first i.v. then per os has proved to be an efficient treatment for acute myelitis. Antibiotherapy is discussed because of the undocumented mechanisms of neurological involvement related to the mycoplasma.


Assuntos
Mycoplasma pneumoniae/patogenicidade , Mielite Transversa/microbiologia , Corticosteroides/uso terapêutico , Criança , DNA Bacteriano , Humanos , Imunoglobulina M/sangue , Masculino , Mycoplasma pneumoniae/genética , Mielite Transversa/tratamento farmacológico , Mielite Transversa/patologia , Reação em Cadeia da Polimerase
10.
Arch Pediatr ; 11(12): 1457-61, 2004 Dec.
Artigo em Francês | MEDLINE | ID: mdl-15596334

RESUMO

UNLABELLED: Discal calcification in childhood is rare. Calcifications are occasionally discovered during routine examinations. Generally, the calcification process is confined to the nucleus pulposus of the intervertebral disc. CASES REPORT: We describe the cases of two children, five and seven years old who presented with acute low back pain. The patients underwent a CT scan, which demonstrated a posterolateral calcified disc hernia. DISCUSSION: Only a few cases with evidence of calcification of the herniated portion of the disc have been previously described. The clinical picture is composed of pain and functional limitation. The radiographic picture consists of the association of morphological and structural alterations of vertebral bodies adjacent to one or more disc calcifications usually centrally sited, sometimes associated with anterior or posterior herniations. The surgical decompression of the nerve root could be necessary.


Assuntos
Calcinose/diagnóstico , Doenças da Coluna Vertebral/diagnóstico , Dor nas Costas/etiologia , Criança , Pré-Escolar , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino
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