Results 261 to 270 of about 5,720 (299)
Some of the next articles are maybe not open access.
The British Journal of Radiology, 1981
A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D. A. Stringer, C. M. Hall
openaire +3 more sources
A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D. A. Stringer, C. M. Hall
openaire +3 more sources
Juvenile hyaline Fibromatose [PDF]
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.
C. Hendricks+3 more
openaire +2 more sources
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 ...
David W. Proops+2 more
openaire +3 more sources
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 ...
David W. Proops+2 more
openaire +3 more sources
The Journal of Dermatology, 2000
AbstractA seventeen‐year‐old Korean girl had a reddish‐brown papular lesion on the nose. Histopathologically, it proved to be a “hyalinizing Spitz nevus” with the characteristic features of a discohesive growth pattern of nevus cells and hyalinized stroma.
Kee-Chan Moon+4 more
openaire +3 more sources
AbstractA seventeen‐year‐old Korean girl had a reddish‐brown papular lesion on the nose. Histopathologically, it proved to be a “hyalinizing Spitz nevus” with the characteristic features of a discohesive growth pattern of nevus cells and hyalinized stroma.
Kee-Chan Moon+4 more
openaire +3 more sources
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
openaire +3 more sources
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.
S. Sollberg+3 more
openaire +3 more sources
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.
S. Sollberg+3 more
openaire +3 more sources
Pulmonary Hyalinizing Granuloma
Chest, 1988A patient with pulmonary hyalinizing granuloma (PHG) is presented. PHG is a rare disease with very specific histological characteristics. Roentgenograms display multiple bilateral pulmonary nodules which may be cavitated. Evidence exists that the nodules are the result of an exaggerated chronic immune response.
S J, Gans, A M, van der Elst, W, Straks
openaire +5 more sources
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.
Andrew Yule Finlay+2 more
openaire +3 more sources
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.
Andrew Yule Finlay+2 more
openaire +3 more sources
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.
openaire +2 more sources
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.
openaire +2 more sources
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.
Liselotte Hochholzer, Samuel A. Yousem
openaire +3 more sources