Literature DB >> 15770507

Tendonitis in variant hyperimmunoglobulinaemia D and periodic fever syndrome--a rare disease with a new symptom.

Sven Armbrust1, Joost P H Drenth, Carmen Schröder, Ester Domning, Ernestine Poeschl, Siegfried K W Wiersbitzky.   

Abstract

UNLABELLED: Hyperimmunoglobulinaemia D syndrome (HIDS) is defined as recurrent fever, generalised lymphadenitis, abdominal pain, arthritis and raised polyclonal serum IgD >100 IU/ml. The cause is a mutation in the mevalonate kinase gene. Other periodic fever syndromes are known. We report a new patient and describe orbital tendonitis as a hitherto unreported symptom
CONCLUSION: Without any underlying cause, the tendonitis must be seen as new symptom of variant hyperimmunoglobulinaemia D syndrome. We speculate that the inflammation of the Tenon spatium is similar to the process of inflammation of the connective tissue in the joint in hyperimmunoglobulinaemia D syndrome where deposits of C3 and IgM are present. Variant hyperimmunoglobulinaemia D syndrome can be present in one family.

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Year:  2005        PMID: 15770507     DOI: 10.1007/s00431-005-1652-9

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  17 in total

Review 1.  Hereditary periodic fever.

Authors:  J P Drenth; J W van der Meer
Journal:  N Engl J Med       Date:  2001-12-13       Impact factor: 91.245

2.  Hyperimmunoglobulinemia D in idiopathic retinal vasculitis.

Authors:  Y Kumano; T Nagato; K Kurihara; H Kikukawa; M Goto; Y Kawano; Y Ohnishi; H Inomata
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1997-06       Impact factor: 3.117

3.  Hyperimmunoglobulinaemia D and periodic fever: a new syndrome.

Authors:  J W van der Meer; J M Vossen; J Radl; J A van Nieuwkoop; C J Meyer; S Lobatto; R van Furth
Journal:  Lancet       Date:  1984-05-19       Impact factor: 79.321

4.  Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.

Authors:  H M Hoffman; J L Mueller; D H Broide; A A Wanderer; R D Kolodner
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

5.  Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

Authors:  J P Drenth; L Cuisset; G Grateau; C Vasseur; S D van de Velde-Visser; J G de Jong; J S Beckmann; J W van der Meer; M Delpech
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

6.  Limited efficacy of thalidomide in the treatment of febrile attacks of the hyper-IgD and periodic fever syndrome: a randomized, double-blind, placebo-controlled trial.

Authors:  J P Drenth; A G Vonk; A Simon; R Powell; J W van der Meer
Journal:  J Pharmacol Exp Ther       Date:  2001-09       Impact factor: 4.030

Review 7.  IgD immune complex vasculitis in a patient with hyperimmunoglobulinemia D and periodic fever.

Authors:  B W Boom; M R Daha; B J Vermeer; J W van der Meer
Journal:  Arch Dermatol       Date:  1990-12

8.  Simvastatin treatment for inflammatory attacks of the hyperimmunoglobulinemia D and periodic fever syndrome.

Authors:  Anna Simon; Elizabeth Drewe; Jos W M van der Meer; Richard J Powell; Richard I Kelley; Anton F H Stalenhoef; Joost P H Drenth
Journal:  Clin Pharmacol Ther       Date:  2004-05       Impact factor: 6.875

9.  Clinical and immunological studies in patients with an increased serum IgD level.

Authors:  I Hiemstra; J M Vossen; J W van der Meer; C M Weemaes; T A Out; B J Zegers
Journal:  J Clin Immunol       Date:  1989-09       Impact factor: 8.317

10.  Cytokine activation during attacks of the hyperimmunoglobulinemia D and periodic fever syndrome.

Authors:  J P Drenth; M van Deuren; J van der Ven-Jongekrijg; C G Schalkwijk; J W van der Meer
Journal:  Blood       Date:  1995-06-15       Impact factor: 22.113

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