Two siblings with juvenile hyaline fibromatosis: Case reports and review of the literature
Küçük Resim Yok
Tarih
1999
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Springer London Ltd
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
In this paper, we describe two siblings with Juvenile Hyaline Fibromatosis (JE-IF) who were diagnosed at the age of 34 and 29 years respectively. JHF is a very congenital disease, mainly diagnosed, in the first few years of life, with less than 40 published cases in literature. All the main clinical features of this syndrome, which may be summarised as multiple subcutaneous rumours, marked gingival hypertrophy, flexion contractures and osteolytic lesions were present in both of these cases. Clinical, radiological and histological differential diagnosis of JHF were made. Recent information about histopathology, treatment and prognosis of JHF was also reviewed.
Açıklama
Anahtar Kelimeler
fibromatosis hyalinica multiplex juvenilis, juvenile hyalin fibromatosis, puretic syndrome, systemic hyalinosis
Kaynak
Clinical Rheumatology
WoS Q Değeri
Q4
Scopus Q Değeri
N/A
Cilt
18
Sayı
3
