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The literature recording cases of the rare juvenile hyaline fibromatosis is reviewed. Gingival enlargement is a regular feature of this entity. A case report and treatment of the gingival lesions are described, and the differential diagnosis and prognosis are discussed.
J G, Camarasa, A, Moreno
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Juvenile non‐hyaline fibromatosis: juvenile hyaline fibromatosis without prominent hyaline changes
Journal of Cutaneous Pathology, 2005Abstract: Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease of the connective tissue. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, osteolytic bone lesions and flexion contractures of the large joints.
Rana Yavuzer, Anadolu +3 more
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Histochemistry of sarcoidotic-hyaline
Pneumonologie Pneumonology, 1976On account of its weaker reactions for tryptophan, tyrosine, proteolipids, and lipoproteins, sarcoidotic-hyaline (Sa. Hy.) is immediately distinguishable from caseosis. However, protein histochemistry fails to differentiate Sa. Hy. from normal (fixed and insoluble postfixed) and pericaseous collagen. Evidence of this is provided by the present study on
G, Barbolini, S, Battaglia
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Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller +3 more
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