دورية أكاديمية
Farber lipogranulomatosis with predominant joint involvement mimicking juvenile idiopathic arthritis.
| العنوان: | Farber lipogranulomatosis with predominant joint involvement mimicking juvenile idiopathic arthritis. |
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| المؤلفون: | Kostik MM; Hospital Pediatric Department, Saint-Petersburg State Pediatric Medical University, Lytovskaya 2, Saint-Petersburg, Russia, 194100, kost-mikhail@yandex.ru., Chikova IA, Avramenko VV, Vasyakina LI, Le Trionnaire E, Chasnyk VG, Levade T |
| المصدر: | Journal of inherited metabolic disease [J Inherit Metab Dis] 2013 Nov; Vol. 36 (6), pp. 1079-80. Date of Electronic Publication: 2013 Feb 06. |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley Country of Publication: United States NLM ID: 7910918 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2665 (Electronic) Linking ISSN: 01418955 NLM ISO Abbreviation: J Inherit Metab Dis Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: 2019- : [Hoboken, NJ] : Wiley Original Publication: [Lancaster, Eng.] MTP Press. |
| مواضيع طبية MeSH: | Arthritis/*diagnosis , Arthritis/*etiology , Arthritis, Juvenile/*diagnosis , Farber Lipogranulomatosis/*complications , Farber Lipogranulomatosis/*diagnosis, Arthritis, Juvenile/etiology ; Child ; Diagnosis, Differential ; Humans ; Male |
| مستخلص: | The case of a 10-year-old boy with Farber lipogranulomatosis with predominant joint involvement, subacute, laryngeal and tongue granulomas, microcytic anemia, elevated ESR and CRP, is presented. The boy had no signs of CNS and internal organ involvement. The disease manifested at 6 months; at 11 months the boy had widespread granulomatous polyarthritis with contractures, and juvenile idiopathic arthritis (JIA) was suggested. All antirheumatic therapies failed. Immunologic assessment revealed elevated serum interleukin-1β, increased T-helper, NK and CD25-positive cells, and circulating immune complexes. Our case with predominant rheumatologic manifestations illustrates a differential diagnosis of JIA. |
| References: | Genomics. 1999 Dec 1;62(2):223-31. (PMID: 10610716) |
| تواريخ الأحداث: | Date Created: 20130207 Date Completed: 20140715 Latest Revision: 20211021 |
| رمز التحديث: | 20240628 |
| DOI: | 10.1007/s10545-012-9573-z |
| PMID: | 23385296 |
| قاعدة البيانات: | MEDLINE |
Find this article in full text from Springer Verlag. 
Full Text Finder | تدمد: | 1573-2665 |
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| DOI: | 10.1007/s10545-012-9573-z |