Results 251 to 260 of about 5,762 (285)
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International Journal of Pediatric Otorhinolaryngology, 1995
A case of juvenile hyaline fibromatosis in a 7-year-old Asian boy is presented. This autosomal recessive inherited condition has not been described in the otolaryngology literature before. We demonstrate the benefits surgical intervention, for treatment of gingival hypertrophy, can bring to the patient and outline the other features of this rare ...
Z P, Shehab, F, Raafat, D W, Proops
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A case of juvenile hyaline fibromatosis in a 7-year-old Asian boy is presented. This autosomal recessive inherited condition has not been described in the otolaryngology literature before. We demonstrate the benefits surgical intervention, for treatment of gingival hypertrophy, can bring to the patient and outline the other features of this rare ...
Z P, Shehab, F, Raafat, D W, Proops
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Der Hautarzt, 1997
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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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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Journal of the American Medical Association, 1958
The clinical signs of hyaline membrane syndrome can simulate the respiratory difficulties seen in any one of a variety of abnormal states. If one could give a "characteristic" feature of this abnormal respiratory situation, it might be said that the infant is born well.
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The clinical signs of hyaline membrane syndrome can simulate the respiratory difficulties seen in any one of a variety of abnormal states. If one could give a "characteristic" feature of this abnormal respiratory situation, it might be said that the infant is born well.
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Der Hautarzt, 2009
Juvenile hyaline fibromatosis is a rare autosomal recessive disease of the connective tissue. We present the case of a 6-year-old normal mental developed boy with confluent pearly papules behind the ears and in the paranasal folds, firm nodules of the scalp, the back and metaphalangs, and severe gingival hypertrophy.
K, Güldner +3 more
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Juvenile hyaline fibromatosis is a rare autosomal recessive disease of the connective tissue. We present the case of a 6-year-old normal mental developed boy with confluent pearly papules behind the ears and in the paranasal folds, firm nodules of the scalp, the back and metaphalangs, and severe gingival hypertrophy.
K, Güldner +3 more
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British Journal of Dermatology, 1983
SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
A Y, Finlay, S D, Ferguson, P J, Holt
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SUMMARY A 4-year-old boy with juvenile hyaline fibromatosis (systemic hyalinosis) is described. The clinical features, pathology and prognosis of this condition are discussed.
A Y, Finlay, S D, Ferguson, P J, Holt
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Pulmonary Hyalinizing Granuloma
American Journal of Clinical Pathology, 1987Pulmonary hyalinizing granulomas are distinct fibrosing lesions of lung, having central whorled deposits of lamellar collagen. Twenty-four cases of this unusual pulmonary lesion are reported herein. Hyalinizing granulomas occur in middle-aged persons and are frequently mistaken for metastatic carcinoma radiographically.
S A, Yousem, L, Hochholzer
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Revista Española de Cardiología (English Edition), 2016
Varon de 44 anos, con antecedentes de sindrome depresivo en tratamiento farmacologico, fallecio como consecuencia de suicidio por ahorcamiento. Durante la autopsia, ademas de los signos propios de la causa de fallecimiento, encontramos 3 nodulos perlados pediculados, de 0,5 cm de diametro en la cara posterior del ventriculo izquierdo (figura 1) y 2 con
Mercè, Subirana-Domènech +2 more
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Varon de 44 anos, con antecedentes de sindrome depresivo en tratamiento farmacologico, fallecio como consecuencia de suicidio por ahorcamiento. Durante la autopsia, ademas de los signos propios de la causa de fallecimiento, encontramos 3 nodulos perlados pediculados, de 0,5 cm de diametro en la cara posterior del ventriculo izquierdo (figura 1) y 2 con
Mercè, Subirana-Domènech +2 more
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Pediatric Dermatology, 2001
Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
M, Larralde +3 more
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Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease with onset in infancy or early childhood. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, and flexion contractures of the large joints. The light and electron microscopic features are very distinctive. Here we report an 8‐month‐old boy
M, Larralde +3 more
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Archives of Dermatology, 1976
A boy had multiple large tumors on the scalp, whitish nodules on the nape and both sides of the neck, hypertrophic gingiva, and severe flexural contractures of hip and knee joints. The histopathologic structure of the tumor was characteristic of juvenile hyalin fibromatosis.
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A boy had multiple large tumors on the scalp, whitish nodules on the nape and both sides of the neck, hypertrophic gingiva, and severe flexural contractures of hip and knee joints. The histopathologic structure of the tumor was characteristic of juvenile hyalin fibromatosis.
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Neuromuscular Disorders, 1994
Muscle biopsy from two unrelated patients, a male aged 40 and a female aged 3, with relatively non-progressive limb weakness since infancy, revealed numerous subsarcolemmal glassy, hyaline appearing bodies present in 20-30% of the fibres. Type 1 fibre predominance was present, and the hyaline bodies were exclusive to type 1 fibres.
R J, Barohn, R A, Brumback, J R, Mendell
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Muscle biopsy from two unrelated patients, a male aged 40 and a female aged 3, with relatively non-progressive limb weakness since infancy, revealed numerous subsarcolemmal glassy, hyaline appearing bodies present in 20-30% of the fibres. Type 1 fibre predominance was present, and the hyaline bodies were exclusive to type 1 fibres.
R J, Barohn, R A, Brumback, J R, Mendell
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