Otitis media as a sign of Wegener's granulomatosis in childhood

被引：0

作者：

Atula, T

Honkanen, V

Tarkkanen, J

Jero, J

机构：

[1] Univ Helsinki, Cent Hosp, Dept Otorhinolaryngol, FI-00029 Helsinki, Finland

[2] Univ Helsinki, Cent Hosp, Dept Pediat, FI-00029 Helsinki, Finland

[3] Univ Helsinki, Cent Hosp, Dept Pathol, FI-00029 Helsinki, Finland

来源：

ACTA OTO-LARYNGOLOGICA | 2000年

关键词：

facial nerve paralysis; middle ear infection; paediatric; Wegener's granulomatosis;

D O I：

暂无

中图分类号：

R76 [耳鼻咽喉科学];

学科分类号：

100213 ;

摘要：

Wegener's granulomatosis (WG) is a rare disease among paediatric patients. Chronic otitis media with or without facial nerve dysfunction is a known manifestation of the disease among adults. A case of a 15-year-old boy with WG, whose initial symptoms were acute otitis media and Facial nerve paralysis, is presented. The otorhinolaryngological manifestations, as well as diagnostic and current treatment modalities in paediatric patients with WG, are discussed.

引用

页码：48 / 50

页数：3

共 50 条

[1] Refractory otitis media as the first manifestation of Wegener's granulomatosis
Antunes Rossini, Bruno Almeida
Bogaz, Eduardo Amaro
Yonamine, Fernando Kaoru
Gurgel Testa, Jose Ricardo
Penido, Norma de Oliveira
[J]. BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY, 2010, 76 (04) : 541 - 541
[2] Chronic otitis media and facial paralysis as a presenting feature of Wegener's granulomatosis
Shiva, Prasad B. N.
Balasubramanian, R.
[J]. SINGAPORE MEDICAL JOURNAL, 2009, 50 (04) : E155 - E157
[3] Wegener's granulomatosis presenting with bilateral chronic otitis media and facial paralysis
Guvenc, M. G.
Edizer, D. T.
Korkut, N.
[J]. TURKISH ARCHIVES OF OTORHINOLARYNGOLOGY, 2010, 48 (01) : 42 - 46
[4] Wegener's granulomatosis in childhood and adolescence
Frosch, M.
[J]. MONATSSCHRIFT KINDERHEILKUNDE, 2006, 154 (09) : 880 - 885
[5] Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
Bohm, Marek
Fernandez, Maria Isabel Gonzalez
Ozen, Seza
Pistorio, Angela
Dolezalova, Pavla
Brogan, Paul
Barbano, Giancarlo
Sengler, Claudia
Klein-Gitelman, Marisa
Quartier, Pierre
Fasth, Anders
Herlin, Troels
Terreri, Maria Teresa R. A.
Nielsen, Susan
van Rossum, Marion A. J.
Avcin, Tadej
Rodolfo Castell, Esteban
Foeldvari, Ivan
Foell, Dirk
Kondi, Anuela
Kone-Paut, Isabelle
Kuester, Rolf-Michael
Michels, Hartmut
Wulffraat, Nico
Ben Amer, Halima
Malattia, Clara
Martini, Alberto
Ruperto, Nicolino
[J]. PEDIATRIC RHEUMATOLOGY, 2014, 12
[6] Clinical features of childhood granulomatosis with polyangiitis (wegener’s granulomatosis)
Marek Bohm
Maria Isabel Gonzalez Fernandez
Seza Ozen
Angela Pistorio
Pavla Dolezalova
Paul Brogan
Giancarlo Barbano
Claudia Sengler
Marisa Klein-Gitelman
Pierre Quartier
Anders Fasth
Troels Herlin
Maria Teresa R A Terreri
Susan Nielsen
Marion A J van Rossum
Tadej Avcin
Esteban Rodolfo Castell
Ivan Foeldvari
Dirk Foell
Anuela Kondi
Isabelle Koné-Paut
Rolf-Michael Kuester
Hartmut Michels
Nico Wulffraat
Halima Ben Amer
Clara Malattia
Alberto Martini
Nicolino Ruperto
[J]. Pediatric Rheumatology, 12
[7] A Rare Vasculitis in Childhood: Wegener's Granulomatosis
Civilibal, Mahmut
Duru, Nilgun Selcuk
Elevli, Murat
Hekimsoy, Sibel
Durali, Kemal
[J]. HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, 2011, 49 (03): : 114 - 116
[8] Granulomatous mastitis as presenting sign of Wegener's granulomatosis
Stappaerts, I
Colpaert, C
Verbraecken, J
Van Marck, E
Vermeire, P
[J]. ACTA CLINICA BELGICA, 1999, 54 (04): : 207 - 210
[9] Early diagnosis of Wegener's granulomatosis presenting with bilateral facial paralysis and bilateral serous otitis media
Ferri, Emanuele
Armato, Enrico
Capuzzo, Paolo
Cavaleri, Stefano
Ianniello, Ferdinando
[J]. AURIS NASUS LARYNX, 2007, 34 (03) : 379 - 382
[10] Wegener's granulomatosis as a rare cause of hemoptysis in childhood
Heckmann, M
Weber, K
Reineck, P
Schüler, D
Geidel, C
Steiss, JO
[J]. KLINISCHE PADIATRIE, 2006, 218 (01): : 20 - 21

← 1 2 3 4 5 →