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Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)

Bohm, Marek (author)
Gonzalez Fernandez, Maria I (author)
Ozen, Seza (author)
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Pistorio, Angela (author)
Dolezalova, Pavla (author)
Brogan, Paul (author)
Barbano, Giancarlo (author)
Sengler, Claudia (author)
Klein-Gitelman, Marisa (author)
Quartier, Pierre (author)
Fasth, Anders, 1945 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Herlin, Troels (author)
Terreri, Maria Teresa R A (author)
Nielsen, Susanne (author)
van Rossum, Marion A J (author)
Avcin, Tadej (author)
Castell, Esteban R (author)
Foeldvari, Ivan (author)
Foell, Dirk (author)
Kondi, Anuela (author)
Koné-Paut, Isabelle (author)
Kuester, Rolf-Michael (author)
Michels, Hartmut (author)
Wulffraat, Nico (author)
Amer, Halima B (author)
Malattia, Clara (author)
Martini, Alberto (author)
Ruperto, Nicolino (author)
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 (creator_code:org_t)
2014-05-26
2014
English.
In: Pediatric Rheumatology. - : Springer Science and Business Media LLC. - 1546-0096. ; 12:18
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Abstract Background Granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis (WG), belongs to the group of ANCA-associated necrotizing vasculitides. This study describes the clinical picture of the disease in a large cohort of GPA paediatric patients.Children with age at diagnosis ≤ 18 years, fulfilling the EULAR/PRINTO/PRES GPA/WG classification criteria were extracted from the PRINTO vasculitis database. The clinical signs/symptoms and laboratory features were analysed before or at the time of diagnosis and at least 3 months thereafter and compared with other paediatric and adult case series (>50 patients) derived from the literature. Findings The 56 children with GPA/WG were predominantly females (68%) and Caucasians (82%) with a median age at disease onset of 11.7 years, and a median delay in diagnosis of 4.2 months. The most frequent organ systems involved before/at the time of diagnosis were ears, nose, throat (91%), constitutional (malaise, fever, weight loss) (89%), respiratory (79%), mucosa and skin (64%), musculoskeletal (59%), and eye (35%), 67% were ANCA-PR3 positive, while haematuria/proteinuria was present in > 50% of the children. In adult series, the frequency of female involvement ranged from 29% to 50% with lower frequencies of constitutional (fever, weight loss), ears, nose, throat (oral/nasal ulceration, otitis/aural discharge), respiratory (tracheal/endobronchial stenosis/obstruction), laboratory involvement and higher frequency of conductive hearing loss than in this paediatric series. Conclusions Paediatric patients compared to adults with GPA/WG have similar pattern of clinical manifestations but different frequencies of organ involvement.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Keyword

Wegener’s granulomatosis; Granulomatosis with polyangiitis; Clinical study; Clinical picture of disease; Comparison with literature

Publication and Content Type

ref (subject category)
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