Juvenile Hyaline Fibromatosis
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Juvenile hyaline fibromatosis (JHF) is a rare, progressive autosomal recessive disease that’s characterized by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present here the case of a 2-yr-old boy with JHF along with a review of the relevant literature. This case demonstrates that JHF should be considered in the differential diagnosis when multiple subcutaneous nodules are observed in the face, head and neck.
Abstract
Juvenile hyaline fibromatosis (JHF) is a rare, progressive autosomal recessive disease that’s characterized by papulonodular skin lesions, soft tissue masses, joint contractures, gingival hypertrophy and osteolytic bone lesions. We present here the case of a 2-yr-old boy with JHF along with a review of the relevant literature. This case demonstrates that JHF should be considered in the differential diagnosis when multiple subcutaneous nodules are observed in the face, head and neck.
참고문헌 (17)
- Uslu H, "Three siblings with juvenile hyaline fibromatosis", J Oral Pathol Med, 36(2), pp.123~125 (2007)
- Kitano Y, "Juvenile hyaline fibromatosis", Arch Dermatol, 112(1), pp.86~88 (1976)
- Fayad MN, "Juvenile hyaline fibromatosis: two new patients and review of the literature", Am J Med Genet, 26(1), pp.123~131 (1987)
- Shehab ZP, "hyaline fibromatosis", Int J Pediatr Otorhinolaryngol, 33(2), pp.179~186 (1995)
- De Rosa G, "Juvenile hyaline fibromatosis: a case report of a localized form?", Am J Dermatopathol, 16(6), pp.624~627 (1994)
- Keser G, "Two siblings with juvenile hyaline fibromatosis: case reports and review of the literature", Clin Rheumatol, 18(3), pp.248~252 (1999)
- Larralde M, "Juvenile hyaline fibromatosis", Pediatr Dermatol, 18(5), pp.400~402 (2001)
- Thomas JE, "Juvenile hyaline fibromatosis: a case report and review of the literature", Int J Dermatol, 43(11), pp.785~789 (2004)
- Remberger K, "Fibromatosis hyalinica multiplex (juvenile hyalin fibromatosis): light microscopic, electron microscopic, immunohistochemical, and biochemical findings", Cancer, 56(3), pp.614~624 (1985)
- Piattelli A, "Juvenile hyaline fibromatosis of gingiva: a case report", J Periodontol, 67(4), pp.451~453 (1996)
- Winik BC, "Juvenile hyaline fibromatosis: ultrastructural study", Am J Dermatopathol, 20(4), pp.373~378 (1998)
- Jacyk WK, "Wentzel LF. Juvenile hyaline fibromatosis in two South African black children", Int J Dermatol, 35(10), pp.740~742 (1996)
- Miyake I, "Juvenile hyaline fibromatosis: case report with five years' follow-up", Am J Dermatopathol, 17(6), pp.584~590 (1995)
- Haleem A, "Juvenile hyaline fibromatosis: morphologic, immunohistochemical, and ultrastructural study of three siblings", Am J Dermatopathol, 24(3), pp.218~224 (2002)
- Ko CJ, "Calcospherules associated with juvenile hyaline fibromatosis", Am J Dermatopathol, 25(1), pp.53~56 (2003)
- Dowling O, "Mutations in capillary morphogenesis gene-2 result in the allelic disorders juvenile hyaline fibromatosis and infantile systemic hyalinosis", Am J Hum Genet, 73(4), pp.957~966 (2003)
- Hanks S, "Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis", Am J Hum Genet, 73(4), pp.791~800 (2003)
