• Aucun résultat trouvé

Les indications inflammatoires :

IV.3 Autres indications :

IV.3.2 Les indications inflammatoires :

Il existe de nombreuses dermatoses dites «sensibles aux stéroïdes» et d'autres affections inflammatoires de la peau susceptibles de faire l'objet d'un traitement par immunosuppresseurs macrolides.

Des rapports de cas et de petites études ont été publiés dans la littérature sur l'utilisation de macrolides dans l'alopécie areata ,la maladie de Behçet, le pyoderma gangrenosum, le lichen sclérodermie ,le lupus érythémateux cutané, le lichen sclerosus, maladie du greffon contre l'hôte et la dermatite atopique et l’urticaire.

Marsland et Griffiths Expert Opin. Enquête Drugs (2004) 13 (2)ont fait une étude sur 129 autres dermatoses. Ces maladies ont toutes des cellules T autoréactives impliqués dans au moins une partie de leur pathogenèse .

Les macrolides sont largement utilisés pour traiter les infections des tissus mous et des voies respiratoires en raison de leur efficacité contre les bactéries à Gram négatif et à Gram positif notamment des staphylococcies cutannées et des infections à streptocoques.

Des preuves croissantes suggèrent que les antibiotiques macrolides ont à la fois des propriétés anti-inflammatoires et immunomodulatrices et sont donc bénéfique pour les maladies inflammatoires notamment en dermatologie pédiatrique. C’est en partant de ce principe que l’utilisation des macrolides a connu un effet rebond durant les dernières décennies en vue de l’accroissement de leurs indications thérapeutiques .Leur succès dans le traitement des maladies inflammatoires de la peau a conduit à leur raffinement pour des applications topiques et systémiques .Malgré le petit nombre d’études éclairant les mécanismes anti-inflammatoires et immunomodulateurs de les macrolides, il existe des preuves solides fournissant un soutien au profit de l'utilisation de ce type de médicament à long terme et à faible dose pour traiter certaines dermatoses inflammatoires sur lesquelles l es macrolides exercent des effets potentiellement immunomodulateurs dans le tels que la dermatite atopique ,le psoriasis, la rosacée , etc …. Bien que des études supplémentaires soient nécessaire, le traitement par macrolides dans certaines dermatoses chroniques a le potentiel de modifier la morbidité et éventuellement améliorer la gravité de ces pathologies. Des essais comparatifs randomisés bien conçus et bien alimentés sont nécessaires.

Dans cette thèse qui traite de la place des macrolides dans le traitement des pathologies dermatologiques en pédiatrie , nous présentons une collection de recherches bibliographiques et d’études cliniques et rapports de cas traitant des avantages potentiels des antibiotiques macrolides dans le traitement de certaines dermatoses qui ont été principalement classés comme non infectieuses.

RESUME

Titre: La place des macrolides en dermatologie pédiatrique Auteur : El Harfaoui Yassine

Rapporteur : Pr Fatima Jabouirik

Mots clés : Macrolide immunosuppresseur ; Dermatologie pédiatrique ; Indication inflammatoire ; Indication infectieuse

Les macrolides sont des molécules à propriétés antibiotiques, qui ont des macrocycles de lactone souvent associés à des sucres neutres ou aminés. Elles constituent une famille d'antibiotiques capables de diffuser dans les tissus, voire à l'intérieur des cellules.

Les antibiotiques macrolides ont à la fois des propriétés anti-inflammatoires et immunomodulatrices et sont donc bénéfiques pour les maladies inflammatoires notamment en dermatologie pédiatrique . C’est en partant de ce principe que l’utilisation des macrolides s’avère relativement efficace dans le traitement de dermatoses inflammatoires tels que la dermatite atopique ,le psoriasis, la rosacée.

Bien que des études supplémentaires soient nécessaire, le traitement par macrolides dans certaines dermatoses chroniques a le potentiel de modifier la morbidité et éventuellement améliorer la gravité de ces pathologies. Des essais comparatifs randomisés bien conçus et bien alimentés sont nécessaires. Leur succès dans le traitement des maladies inflammatoires de la peau a conduit à leur raffinement pour des applications topiques et systémiques .

Malgré le petit nombre d’études éclairant les mécanismes anti-inflammatoires et immunomodulateurs des macrolides, il existe des données solides fournissant un soutien au profit de l'utilisation de ce type de médicament à long terme et à faible dose .

Cependant la recherche d’autres macrolides immunosuppresseurs a conduit au développement de nouveaux agents dotés de profils moléculaires améliorés pour le traitement des maladies de la peau.

ABSTRACT

Title : The place of macrolides in pediatric dermatology Author :El Harfaoui Yassine

Reporter : Pr Fatima Jabouirik

Keywords : Macrolide ; Immunosuppressive ; Pediatric Dermatology ; Inflammatory Indication ; Infectious indication

Macrolides are molecules with antibiotic properties, which have lactone macrocycles often associated with neutral or amine sugars. They constitute a family of antibiotics able to diffuse in the tissues, even inside the cells.

The macrolide are antibiotics that have both anti-inflammatory and immunomodulatory properties and are therefore beneficial for inflammatory diseases, particularly in pediatric dermatology. It is from this principle that the use of macrolides is relatively effective in the treatment of inflammatory dermatoses such as atopic dermatitis, psoriasis, rosacea .

Although additional studies are needed, treatment with macrolides in some chronic dermatoses has the potential to alter morbidity and possibly improve the severity of these conditions. Well-designed and well-informed randomized controlled trials are needed. Their success in the treatment of inflammatory skin diseases has led to their refinement for topical and systemic applications.

Despite the small number of studies illuminating the anti-inflammatory and immunomodulatory mechanisms of macrolides, there is strong evidence supporting benefit from the use of this type of drug in the long term and low dose.

However the search for other immunosuppressive macrolides has led to the development of new agents with improved molecular profiles for the treatment of skin diseases.

ﺺﺨﻠﻣ

ناﻮﻨﻌﻟا لﺎﻔطﻸﻟ ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا ﻲﻓ تاﺪﯿﻟوﺮﻛﺎﻤﻟا ﻊﺿو : فﺮط ﻦﻣ ﻦﯿﺳﺎﯾ يوﺎﻓﺮﺤﻟا : فﺮﺸﻤﻟا ﻚﯾرﻮﺑﺎﺟ ﺔﻤطﺎﻗ رﻮﺴﯿﻓوﺮﺒﻟا : ﺔﯿﺳﺎﺳﻷا تﺎﻤﻠﻜﻟا ،ﺔﻋﺎﻨﻤﻟا تﺎﻄﺒﺜﻣ ،ﺪﯿﻟوﺮﻛﺎﻤﻟا : طﻷا ﺐط ،ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا ﻔ ،ﻲﻠﺒﮭﻤﻟا بﺎﮭﺘﻟﻻا ،لﺎ ﺔﯾﺪﻌﻣ ةرﺎﺷإ ﻋ ﺐﻟﺎﻐﻟا ﻲﻓ يﻮﺘﺤﺗ ﻲﺘﻟاو ،ﺔﯾﻮﯿﺤﻟا تادﺎﻀﻤﻠﻟ ﺺﺋﺎﺼﺧ تاذ تﺎﺌﯾﺰﺟ ﻲھ تاﺪﯿﻟوﺮﻛﺎﻤﻟا ﻰﻠ ةﺪﯾﺎﺤﻤﻟا تﺎﯾﺮﻜﺴﻟﺎﺑ ﺔﻄﺒﺗﺮﻣ ﺔﯿﻧﻮﺘﻛﻻ ﺔﯿﻧﻮﺘﻛﺎﻣ تﺎﺟارد ﻦﻣ ﺔﻠﺋﺎﻋ ﻞﻜﺸﺗ ﺎﮭﻧإ ﺔﯿﻨﻣﻷا وأ ﺔﯾﻮﯿﺤﻟا تادﺎﻀﻤﻟا .ﺎﯾﻼﺨﻟا ﻞﺧاد ﻰﺘﺣ ،ﺔﺠﺴﻧﻷا ﻲﻓ رﺎﺸﺘﻧﻻا ﻰﻠﻋ ةردﺎﻗ ةﺪﯿﻔﻣ ﻲﮭﻓ ﻲﻟﺎﺘﻟﺎﺑو ﺔﻋﺎﻨﻤﻟاو تﺎﺑﺎﮭﺘﻟﻼﻟ ةدﺎﻀﻣ صاﻮﺧ ﺪﯾﻻوﺮﻛﺎﻤﻟ ﺔﯾﻮﯿﺤﻟا تادﺎﻀﻤﻠﻟ ضاﺮﻣﻸﻟ ﺔﯿﺑﺎﮭﺘﻟﻻا ماﺪﺨﺘﺳا نأ أﺪﺒﻤﻟا اﺬھ ﻦﻣ .لﺎﻔطﻷا ىﺪﻟ ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا ﻲﻓ ﺔﺻﺎﺧ ، جﻼﻋ ﻲﻓ ﺎﯿﺒﺴﻧ لﺎﻌﻓ تاﺪﯿﻟوﺮﻛﺎﻤﻟا ﺔﯿﻓﺪﺼﻟاو ﻲﺒﺗﺄﺘﻟا ﺪﻠﺠﻟا بﺎﮭﺘﻟا ﻞﺜﻣ ﺔﯿﺑﺎﮭﺘﻟﻻا ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا تاﺪﯿﻟوﺮﻛﺎﻤﻟﺎﺑ جﻼﻌﻟا نﺈﻓ ،تﺎﺳارﺪﻟا ﻦﻣ ﺪﯾﺰﻣ ﻰﻟإ ﺔﺟﺎﺤﻟا ﻦﻣ ﻢﻏﺮﻟا ﻰﻠﻋ .ﻚﻟذ ﻰﻟإ ﺎﻣو ﺔﯾﺪﯾرﻮﻟاو هﺬھ ةﺪﺷ ﻦﯿﺴﺤﺗ ﺎﻤﺑرو ﺔﺿاﺮﻤﻟا ﺮﯿﯿﻐﺗ ﻰﻠﻋ ةرﺪﻘﻟا ﮫﻟ ﺔﻨﻣﺰﻤﻟا ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا ﺾﻌﺑ ﻲﻓ ا اﻮﺷ تاذ ةﺎﺸﻌﻣ برﺎﺠﺘﻟ ﺔﺟﺎﺣ ﻚﻟﺎﻨھ . تﻻﺎﺤﻟ ھ ﻲﻓ ﺎﮭﺣﺎﺠﻧ ىدأ ةﺮﯿﻨﺘﺴﻣو اﺪﯿﺟ ﺎﻤﯿﻤﺼﺗ ﺔﻤﻤﺼﻣ ﺪ ﻮﻤﻟا تﺎﻘﯿﺒﻄﺘﻠﻟ ﺎﮭﻨﯿﺴﺤﺗ ﻰﻟإ ﺔﯿﺑﺎﮭﺘﻟﻻا ﺪﻠﺠﻟا ضاﺮﻣأ جﻼﻋ ﺿ ﺔﯾزﺎﮭﺠﻟاو ﺔﯿﻌ . ،ﺔﻋﺎﻨﻤﻟاو تﺎﺑﺎﮭﺘﻟﻼﻟ ةدﺎﻀﻤﻟا تاﺪﯿﻟوﺮﻛﺎﻤﻟا تﺎﯿﻟآ ءﻲﻀﺗ ﻲﺘﻟا تﺎﺳارﺪﻟا ﺔﻠﻗ ﻦﻣ ﻢﻏﺮﻟا ﻰﻠﻋو ﻲﻓ تارﺪﺨﻤﻟا ﻦﻣ عﻮﻨﻟا اﺬھ ماﺪﺨﺘﺳا ﻦﻣ ةدﺎﻔﺘﺳﻻا ﻢﻋﺪﺗ ﺔﯾﻮﻗ ﺔﻟدأ كﺎﻨﮭﻓ ا ﺔﻀﻔﺨﻨﻣو ﻞﯾﻮﻄﻟا ىﺪﻤﻟ .ﺔﻋﺮﺠﻟا ةﺪﯾﺪﺟ ﻞﻣاﻮﻋ ﺮﯾﻮﻄﺗ ﻰﻟإ ىﺮﺧﻷا ﺔﻌﺗﺎﻨﻤﻠﻟ ﺔﻄﺒﺜﻤﻟا تاﺪﯿﻟوﺮﻛﺎﻤﻟا ﻦﻋ ﺚﺤﺒﻟا ىدأ ﺪﻘﻓ ، ﻚﻟذ ﻊﻣو ﺰﺟ ﺢﻣﻼﻣ ناذ ﯾ . ﺔﯾﺪﻠﺠﻟا ضاﺮﻣﻷا جﻼﻌﻟ ﺔﻨﺴﺤﻣ ﺔﯿﺌ

[1] http://127.0.0.1/ressources/cours%20internat/section5/25macrolides-et-apparentes.pdf [2] https://docplayer.fr/8883877-Macrolides-et-apparentes-groupe-mls-macrolides-lincosamines-synergistines.html [3] http://unt-ori2.crihan.fr/unspf/2014_Rennes_Tomasi_Macrolides/co/Biogenese.html [4] https://pharmatox.files.wordpress.com/2016/01/6-macrolides-sby-2015.pdf [5] https://sci-hub.tw/https://doi.org/10.1016/S0515-3700(08)70116-2 [6] http://127.0.0.1/ressources/cours%20internat/section5/25macrolides-et-apparentes.pdf [7] https://pharmacomedicale.org/medicaments/par-specialites/item/macrolides [8] https://medicament.ooreka.fr/astuce/voir/520591/macrolides [9] https://sci-hub.tw/https://doi.org/10.1016/S0515-3700(08)70116-2 [10] https://sci-hub.tw/https://doi.org/10.1016/S0515-3700(08)70116-2 [11] file:///C:/Users/yaya/Downloads/25macrolides-et-apparentes.pdf [12] file:///C:/Users/yaya/Downloads/25macrolides-et-apparentes.pdf [13] file:///C:/Users/yaya/Downloads/25macrolides-et-apparentes.pdf [14] https://sci-hub.tw/https://doi.org/10.1016/S0515-3700(08)70116-2 [15] http://127.0.0.1/ressources/cours%20internat/section5/25macrolides-et-apparentes.pdf [16] http://127.0.0.1/ressources/cours%20internat/section5/25macrolides-et-apparentes.pdf

[17] Lassus A. Comparative studies of azithromycin in skin and soft tissue

infections and sexually transmitted infectionsby Neisseria and

Chlamydia species. J AntimicrobChemother 1990;25(Suppl A):115–21

[18] Amaya-Tapia G, Aguirre-Avalos G, Andrade-Villanueva J, et al.

Once-daily azithromycin in the treatment of adult skin and skin-structure infections. J Antimicrob Chemother 1993;31(Suppl E):129–35

[19] Langtry HD, Balfour JA. Azithromycin. A review of its use in paediatric

infectious diseases. Drugs 1998;56:273–97

[20] Treadway G, Reisman A. Tolerability of 3-day, oncedaily azithromycin

suspension versus standard treatments for community-acquired paediatric infectious diseases. Int J Antimicrob Agents 2001;18:427–31.

[21] Fernandez-Obregon AC. Azithromycin for the treatment of acne. Int J

Dermatol 2000;39:45–50

[22] Gruber F, Grubisic-Greblo H, Kastelan M, et al. Azithromycin compared

with minocycline in the treatment of acne comedonica and papulo-pustulosa. J Chemother 1998;10:469–73

[23] Parsad D, Pandhi R, Nagpal R, Negi KS. Azithromycin monthly pulse vs

daily doxycycline in the treatment of acne vulgaris. J Dermatol 2001;28:1–4

[24] Elewski BE. A novel treatment for acne vulgaris and rosacea. J Eur Acad

Dermatol Venereol 2000;14:423–4. 26. Bowden FJ, Savage J. Donovanosis: treatment with azithromycin. Int J STD AIDS 1998;9:61–

[25] Bowden FJ, Savage J. Donovanosis: treatment with azithromycin. Int J

STD AIDS 1998;9:61–2

[26] Woodward C, Fisher MA. Drug treatment of common STDs: Part I.

Herpes, syphilis, urethritis, chlamydia and gonorrhea. Am Fam Phys 1999;60:1387–94.

[27] Martin DH, Sargent SJ, Wendel GD, Jr, et al. Comparison of

azithromycin and ceftriaxone for the treatment of chancroid. Clin Infect Dis 1995;21:409–14.

[28] Wolkenstein P, Grob JJ, Bastuji-Garin S, Ruszczynski S, Roujuea JC,

Revuz J. French people and skin diseases: results of a survey using a representative sample. Arch Dermatol 2003;139:1614—9.

[29] Pawin H, Chivot M, Beylot C, Faure M, Poli F, Revuz J, et al. Living

with acne. A study of adolescents’ personal experiences. Dermatology 2007;215:308—14.

[30] Ballanger F, Baudry P, N’Guyen JM, Khammari A, Dréno B. Heredity: a

prognostic factor for acne. Dermatology 2006;212:145—9.

[31] Capitanio B, Sinagra JL, Ottaviani M, Bordignon V, Amantea A,

Picardo M. Smoker’s acne: a new clinical entity? Br J Dermatol 2007;157:1040—85.

[32] Zouboulis CC, Böhm M. Neuroendocrine regulation of sebocytes: a

pathogenetic link between stress and acne. Exp Dermatol 2004;13:31— 5.

[33] Burkhart CG, Burkhart CN. Expanding the microcomedone theory and

acne therapeutics: Propionibacterium acnes biofilm produces biological glue that holds corneocytes together to form plug. J Am Acad Dermatol 2007;57:722—4.

[34] Jeremy AH, Holland DB, Roberts SG, Thomson KF, Cunliffe WJ.

Inflammatory events are involved in acne lesion initiation. J Invest Dermatol 2003;121:20—7.

[35] Jarrousse V, Castex-Rizzi N, Khammari A, Charveron M, Dréno B.

Modulation of integrins and filaggrin expression by Propionibacterium acnes extracts on keratinocytes. Arch Dermatol Res 2007;299:441—7.

[36] Plantin P, Société franc¸aise de dermatologie pédiatrique. Acne in the

newborn and infants. Ann Dermatol Vénéréol 2008;135:518—20.

[37] Krakowski AC, Eichenfield LF. Pediatric acne: clinical presentations,

evaluation, and management. J Drugs Dermatol 2007;6:589—93.

[38] Cunliffe W, Baron S, Coulson IH. A clinical and therapeutic study of 29

patients with infantile acne. Br J Dermatol 2001;145:463—6.

[39] Herane MI, Ando I. Acne in infancy and acne genetics. Dermatology

2003;206:24—8.

[40] Jansen T, Burgdorf WH, Plewig G. Pathogenesis and treatment of acne

in childhood. Pediatr Dermatol 1997;14:17—21.

[41] Hello M, Prey S, Léauté-Labrèze C, Khammari A, Dréno B, Stalder JF,

[42] Barnes CJ, Eichenfield LF, Lee J, Cunningham BB. A practical approach

for the use of oral isotretinoine in infantile acne. Pediatr Dermatol 2005;22:166—9.

[43] Chew EW, Bingham A, Durrows D. Incidence of acne vulgaris in

patients with infantile acne. Clin Exp Dermatol 1990;15:376—7.

[44] Marcoux D, Mccuaig CC, Powell J. Prepubertal acne: clinical

presentation, evaluation and treatment. J Cutan Med Surg 1998;2:2—6.

[45] Mann MW, Ellis SS, Mallory SB. Infantile acne as initial sign of an

adrenocortical tumor. J Am Acad Dermatol 2007;56(Suppl. 2):S15—8.

[46] Torrelo A, Pastor MA, Zambrano A. Severe acne infantum successfully

treated with isotretinoin. Pediatr Dermatol 2005;22:357—9.

[47] Chivot M. Poussées inflammatoires et aggravations d’acné sous

isotrétinoïne orale. Ann Dermatol Venereol 2001;128:224—8.

[48] Faure M, Pawin H, Poli F, Revuz J, Beylot C, Chivot M, et al. Factors

influencing the clinical evaluation of facial acne. Acta Derm Venereol 2009;89:369—71.

[49] Bernier V, Weill FX, Hirigoyen V, Elleua C, Feyler A, Labreze C, et al.

Skin colonization by Malassezia species in neonates. A prospective study and relationship with neonatal cephalic pustulosis. Arch Dermatol 2002;138:215—8.

[50] Thiboutot DM, Weiss J, Bucko A, Eichenfield L, Jones T, Clark S, et al.

Adapalen-benzoyl peroxide, a fixed-dose combination for the treatment of acne vulgaris: results of a multicenter, randomized, controlled study. J

[51] Traitement de l’acné par voie locale et générale. Recommandations.

Afssaps, novembre 2007.

[52] Strahan JE, Raimer S. Isotretinoin and the controversy of psychiatric

adverse effects. Int J Dermatol 2006;45:789—99.

[53] Dreno B, Chosidow O. Isotretinoin and psychiatric sides effects: facts

and hypothesis. Expert Rev Dermatol 2008;3: 711—20.

[54] Gold MH. Acne vulgaris: lasers, light sources and photodynamic

therapy-an update 2007. Expert Rev Anti Infect Ther 2007;5:1059—69.

[55] Goulden V. Guidelines for the management of acne vulgaris in

adolescents. Pediatr Drugs 2003;5:301—13.

[56] Cantatore-Francis JL, Glick SA. Childhood acne: evaluation and

management. Dermatol Ther 2006;19:202—9.

[57] Leauté-Labrèze C, Gautier C, Labbé L, Taieb A. Acné infantile et

isotrétinoïne. Ann Dermatol Venereol 1998;125:132—4.

[58] Sarazin F, Dompmartin A, Nivot S, Letessier D, Leroy D. Treatment of

an infantile acne with oral isotretinoin. Eur J Dermatol 2004;14:71—2

[59] http://www.afssaps.fr/var/afssaps_site/storage/original/application/d82a1

ce33e d6ece279f8a5e04c6c0551.pdf

[60] http://www.infectiologie.com/site/medias/_documents/consensus/erysipe

lelong-00.pdf

[61] D. D. Balci, N. Duran, B. Ozer, R. Gunessacar, Y. Onlen, and J. Z.

super-antigen production in patients with psoriasis,” European Journal of Dermatology, vol. 19, pp. 238– 242, 2009.

[62] M. Komine and K. Tamaki, “An open trial of oral macrolide treatment

for psoriasis vulgaris,” Journal of Dermatology, vol. 27, no. 8, pp. 508– 512, 2000

[63] J. Tamaoki, J. Kadota, and H. Takizawa, “Clinical implications of the

immunomodulatory effects of macrolides,” The American Journal of Medicine, vol. 117, supplement 9, pp. 5s–11s, 2004

[64] C. M. Owen, R. J. G. Chalmers, T. O’Sullivan, and C. E. M. Griffiths,

“A systematic review of antistreptococcal interventions for guttate and chronic plaque psoriasis,” British Journal of Dermatology, vol. 145, no. 6, pp. 886–890, 2001.

[65] J. K. Wilson, S. N. Al-Suwaidan, D. Krowchuk, and S. R. Feldman,

“Treatment of psoriasis in children: is there a role for antibiotic therapy and tonsillectomy?” Pediatric Dermatology, vol. 20, no. 1, pp. 11–15, 2003.

[66] H. Valdimarsson, H. Sigmundsdottir, and I. Jonsdottir, “Is psoriasis

induced by streptococcal super antigens and maintained by M- protein specific T cells that cross react with keratin?” Clinical & Experimental Immunology, vol. 107, pp. 21–24, 1997.

[67] J. C. Prinz, “Psoriasis vulgaris- a sterile anti-bacterial skin reaction

mediated by cross reactive T cells? An immunological view of the patho physiology of psoriasis,” Clinical and Experimental Dermatology, vol. 26, pp. 326–332, 2001.

[68] C. Matzaroglou, D. Velissaris, A. Karageorgos, M. Marangos, E.

Panagiotopoulos, and M. Karanikolas, “SAPHO syndrome diagnosis and treatment: report of five cases and review of the literature,” The Open Orthopaedics Journal, vol. 3, pp. 100–106, 2009.

[69] A. Ohshima, M. Takigawa, and Y. Tokura, “CD8+ cell changes in

psoriasis associated with roxithromycin-induced clinical improvement,” European Journal of Dermatology, vol. 11, no. 5, pp. 410–415, 2001

[70] S. Konno, M. Adachi, K. Asano, K. Okamoto, and T. Takahashi,

“Inhibition of human T-lymphocyte activation by macrolide antibiotic, roxithromycin,” Life Sciences, vol. 51, no. 24, pp. 231–236, 1992

[71] H. Wakita, Y. Tokura, F. Furukawa, and M. Takigawa, “The macrolide

antibiotic, roxithromycin suppresses IFNγ-mediated immunological functions of cultured normal human keratinocytes,” Biological and Pharmaceutical Bulletin, vol. 19, no. 2, pp. 224–227, 1996.

[72] V. N. Saxena and J. Dogra, “Long-term oral azithromycin in chronic

plaque psoriasis: a controlled trial,” European Journal of Dermatology, vol. 20, no. 3, pp. 329–333, 2010.

[73] K. Tamaki, “Antipruritic effect of macrolide antibiotics,” Journal of

Dermatology, vol. 27, no. 1, pp. 66–67, 2000

[74] M. Polat, N. Lenk, B. Yalcin et al., “Efficacy of erythromycin for

psoriasis vulgaris,” Clinical and Experimental Dermatology, vol. 32, no. 3, pp. 295–297, 2007

[76] J. Q. Del Rosso, “Systemic therapy for rosacea: focus on oral antibiotic

therapy and safety,” Cutis, vol. 66, supplement 4, pp. 7–13, 2000.

[77] P. Humbert, P. Treffel, J. F. Chapuis, S. Buchet, C. Derancourt, and P.

Agache, “The tetracyclines in dermatology,” Journal of the American Academy of Dermatology, vol. 25, no. 4, pp. 691– 697, 1991.

[78] O. Bakar, Z. Demirc¸ay, M. Yuksel, G. Haklar, and Y. Sanisoglu, “The

effect of azithromycin on reactive oxygen species in rosacea,” Clinical and Experimental Dermatology, vol. 32, no. 2, pp. 197–200, 2007.

[79] A. Fernandez-Obregon, “Oral use of azithromycin for the treatment of

acne rosacea,” Archives of Dermatology, vol. 140, no. 4, pp. 489–490, 2004.

[80] S. Modi, M. Harting, and T. Rosen, “Azithromycin as an alternative

rosacea therapy when tetracyclines prove problematic,” Journal of Drugs in Dermatology, vol. 7, no. 9, pp. 898–899, 2008.

[81] M. Akhyani, A. H. Ehsani, M. Ghiasi, and A. K. Jafari, “Comparison of

efficacy of azithromycin vs. doxycycline in the treatment of rosacea: a randomized open clinical trial,” International Journal of Dermatology, vol. 47, no. 3, pp. 284– 288, 2008

[82] J. H. Kim, Y. S. Oh, and E. H. Choi, “Oral azithromycin for treatment of

intractable rosacea,” Journal of Korean Medical Science, vol. 26, no. 5, pp. 694–696, 2011.

[83] A. M. Chamot, C. L. Benhamou, M. F. Kahn, L. Beraneck, G. Kaplan,

and A. Prost, “Acne- pustulosis- hyperostosis- osteitis syndrome. Results of a national survey: 85 cases,” Revue du Rhumatisme et des Maladies Osteo-Articulaires, vol. 54, pp. 187–196, 1987

[84] M. Colina, A. Lo Monaco, M. Khodeir, and F. Trotta,

“Propionibacterium acnes and SAPHO syndrome: a case report and literature review,” Clinical and Experimental Rheumatology, vol. 25, no. 3, pp. 457–460, 2007.

[85] T. Schaeverbeke, L. Lequen, B. de Barbeyrac et al., “Propionibacterium

acnes isolated from synovial tissue and fluid in a patient with oligoarthritis associated with acne and pustulosis,” Arthritis & Rheumatism, vol. 41, pp. 1889–1893, 1998

[86] T. Kirchhoff, S. Merkesdal, H. Rosenthal et al., “Diagnostic

management of patients with SAPHO syndrome: use of MR imaging to guide bone biopsy at CT for microbiological and histological work-up,” European Radiology, vol. 13, no. 10, pp. 2304–2308, 2003.

[87] G. Assmann, O. Kueck, T. Kirchhoff et al., “Efficacy of antibiotic

therapy for SAPHO syndrome is lost after its discontinuation: an interventional study,” Arthritis Research and Therapy, vol. 11, no. 5, article R140, 2009

[88] C. Matzaroglou, D. Velissaris, A. Karageorgos, M. Marangos, E.

Panagiotopoulos, and M. Karanikolas, “SAPHO syndrome diagnosis and treatment: report of five cases and review of the literature,” The Open

[89] P. K. Sharma, T. P. Yadav, R. K. Gautam, N. Taneja, and L.

Satyanarayana, “Erythromycin pityriasis rosea: a doubleblind, placebo-controlled clinical trial,” Journal of the American Academy of Dermatology, vol. 42, no. 2, pp. 241–244, 2000.

[90] A. Rasi, L. Tajziehchi, and S. Savabi-Nasab, “Oral erythromycin is

ineffective in the treatment of pityriasis rosea,” Journal of Drugs in Dermatology, vol. 7, no. 1, pp. 35–38, 2008.

[91] A. Chuh, A. Lee, V. Zawar, G. Sciallia, and W. Kempf, “Pityriasis

rosea—an update,” Indian Journal of Dermatology, Venereology and Leprology, vol. 71, no. 5, pp. 311–315, 2005.

[92] H. Mensing and S. Krausse, “Erythromycin treatment for bullous

pemphigoid,” Medizinische Klinik, vol. 85, no. 8, pp. 481–484, 1990

[93] G. Altomare, G. L. Capella, C. Fracchiolla, and E. Frigerio, “Treatment

of bullous pemphigoid with erythromycin: a reappraisal,” European Journal of Dermatology, vol. 9, no. 7, pp. 583–585, 1999

[94] B. J. Fox, R. B. Odom, and R. F. Findlay, “Erythromycin therapy in

bullous pemphigoid: possible anti-inflammatory effects,” Journal of the American Academy of Dermatology, vol. 7, no. 4, pp. 504–510, 1982.

[95] STEWART GE 2nd: Histopathology of chronic urticaria. Clin. Rev.

Allergy. Immunol. (2002) 23:195-200

[96] HIDE M, FRANCIS DM, GRATTAN CE et al.: Autoantibodies against

the high- affinity IgE receptor as a cause of histamine release in chronic urticaria.N. Engl. J. Med. (1993) 328:1599-1604

[97] KIKUCHI Y, KAPLAN AP: A role for C5a in augmenting IgG-dependent

histamine release from basophils in chronic urticaria.

J. Allergy Clin. Immunol.(2002)

109:114-118.

[98] OKAYAMA Y, BENYON RC, LOWMAN MA, CHURCH MK: In vitro

effects of H1-antihistamines on histamine and PGD2 release from mast cells of human lung, tonsil, and skin. Allergy (1994) 49:246-253

[99] KAPLAN AP: Clinical practice. Chronic urticaria and angioedema. N.

Engl. J. Med. (2002) 346:175-179.

Easy-to-digest background article on clinical aspects of urticaria

[100] ERBAGCI Z: The leukotriene receptor antagonist montelukast in the

treatment of chronic idiopathic urticaria: a single-blind, placebo-controlled, crossover clinical study. J. Allergy Clin. Immunol.(2002)

110:484-488.

[101] GRATTAN CE, O’DONNELL BF, FRANCIS DM et al.: Randomized

double- blind study of cyclosporin in chronic ‘idiopathic’ urticaria.Br. J.

Dermatol. (2000) 143:365-372.

[102] ELLIS CN, DRAKE LA, PRENDERGAST MM et al.: Cost of atopic

dermatitis and eczema in the United States. J. Am. Acad. Dermatol.(2002)

46:361-370

[103] COOKSON WO, MOFFATT MF: The genetics of atopic dermatitis.Curr. Opin. Allergy Clin. Immunol.(2002) 2:383-387.

[104] LEUNG DY: Atopic dermatitis and the immune system: the role of

superantigens and bacteria. J. Am. Acad. Dermatol.(2001) 45:S13-16.

[105] AKDIS M, TRAUTMANN A, KLUNKER S, BLASER K, AKDIS CA:

Cytokine network and dysregulated apoptosis in atopic dermatitis. Acta

Odontol. Scand. (2001) 59:178-182

[106]

Au moment d'être admis à devenir membre de la profession médicale, je

Documents relatifs