Étude de onze nouveaux cas congolais de maladie de Kawasaki

作者: J. R. Mabiala Babela , L. C. Ollandzobo Ikobo , R. E. Nika , G. Moyen

DOI: 10.1007/S13149-015-0445-2

关键词: AirwayRetrospective cohort studyIncidence (epidemiology)Angular cheilitisMucocutaneous Lymph Node SyndromeMedicineSurgeryKawasaki diseaseErythemaEpidemiology

摘要: Kawasaki's disease (KD) is a rarely described entity in Africa. The purpose of this work to describe the clinical, biological and evolutionary aspects KD Congolese child. This retrospective study 11 cases collected from 2003 2014 at University Hospital Brazzaville. diagnosis was based on criteria proposed by Mucocutaneous Lymph Node Syndrome Research Commitee validated Center for Disease Control grouping major originally Kawasaki updated American Heart Association. sex-ratioM/F 2.7 mean age 16.5 ± 5.9 months (range 9 43 months). average intake time 12.8 days 6 30). In nine there complete form. symptoms began with an invasion upper airway 8 cases. Achieving oropharyngeal form oral enanthema strawberry tongue / or angular cheilitis; it associated perineal erythema 7 Reaching end realized swelling and/or redness peeling finger gloves flap toes. latter occurred 3.5 16) after start fever. treatment acetylsalicylic acid administered all children, within varying between 4 15 admission. defervescence obtained 5.3 2.6 11). hospital stay 16.6 9.7 (range: 25 days). evolution discharge considered favorable However, no control echocardiography performed. remains ubiquitous condition but variable incidence one continent another. arrival twodimensional ultrasound should enable systematic investigation coronary abnormalities catch up unnoticed past also prevent complications related there.

参考文章(23)
Alexandra F Freeman, Stanford T Shulman, Kawasaki disease: summary of the American Heart Association guidelines. American Family Physician. ,vol. 74, pp. 1141- 1148 ,(2006)
Kensuke Harada, Intravenous γ‐Globulin Treatment in Kawasaki Disease Pediatrics International. ,vol. 33, pp. 805- 810 ,(1991) , 10.1111/J.1442-200X.1991.TB02612.X
M. Caquard, G. Parlier, D. Siret, Forme familiale de la maladie de Kawasaki : à propos de 2 cas dans une fratrie Archives De Pediatrie. ,vol. 13, pp. 453- 455 ,(2006) , 10.1016/J.ARCPED.2006.02.012
HIROSHI YANAGAWA, YOSIKAZU NAKAMURA, MAYUMI YASHIRO, RITEI UEHARA, IZUMI OKI, KAZUNORI KAYABA, Incidence of Kawasaki disease in Japan: the nationwide surveys of 1999-2002. Pediatrics International. ,vol. 48, pp. 356- 361 ,(2006) , 10.1111/J.1442-200X.2006.02221.X
Donald Y.M. Leung, H.Cody Meissner, Stanford T. Shulman, Wilbert H. Mason, Michael A. Gerber, Mary P. Glode, Barry L. Myones, J.Gary Wheeler, Robin Ruthazer, Patrick M. Schlievert, Prevalence of superantigen-secreting bacteria in patients with Kawasaki disease The Journal of Pediatrics. ,vol. 140, pp. 742- 746 ,(2002) , 10.1067/MPD.2002.123664
B Schiller, A Fasth, G Bjorkhem, G Elinder, Kawasaki disease in Sweden: incidence and clinical features. Acta Paediatrica. ,vol. 84, pp. 769- 774 ,(1995) , 10.1111/J.1651-2227.1995.TB13753.X
A. Bourrillon, La maladie de Kawasaki sous toutes ses facettes Archives De Pediatrie. ,vol. 15, pp. 825- 828 ,(2008) , 10.1016/S0929-693X(08)71928-6
Ritei Uehara, Ermias D. Belay, Epidemiology of Kawasaki Disease in Asia, Europe, and the United States Journal of Epidemiology. ,vol. 22, pp. 79- 85 ,(2012) , 10.2188/JEA.JE20110131
Ahmad Shamsizadeh, Tahereh Ziaei Kajbaf, Maryam Razavi, Bahman Cheraghian, Clinical and epidemiological characteristics of kawasaki disease. Jundishapur Journal of Microbiology. ,vol. 7, pp. 0- 0 ,(2014) , 10.5812/JJM.11014