Results 201 to 210 of about 86,714 (241)
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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
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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
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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 ...
David W. Proops +2 more
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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 ...
David W. Proops +2 more
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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
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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
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Surface properties in relation to atelectasis and hyaline membrane disease.
A M A Journal of Diseases of Children, 1959Recent observations suggest that a low surface tension may be an important attribute of the lining of the air passages of the lung.1-4The purpose of this paper is to present evidence that the material responsible for such a low surface tension is absent ...
M. Avery, J. Mead
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Hyaline Droplets in Kupffer Cells: A Novel Diagnostic Clue for Autoimmune Hepatitis
American Journal of Surgical Pathology, 2015Pediatric autoimmune hepatitis (AIH) is relatively common and has a characteristic but relatively nonspecific histopathology with a usually prominent lymphoplasmacytic infiltrate.
Suzanne M. Tucker +2 more
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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
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Cancer, 1972
A clinicopathologic analysis of 81 cases of giant lymph node hyperplasia was undertaken, with review of previously reported cases. Most of the lesions were intrathoracic.
A. Keller, L. Hochholzer, B. Castleman
semanticscholar +1 more source
A clinicopathologic analysis of 81 cases of giant lymph node hyperplasia was undertaken, with review of previously reported cases. Most of the lesions were intrathoracic.
A. Keller, L. Hochholzer, B. Castleman
semanticscholar +1 more source
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
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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.
S. Sollberg +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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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
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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.
Andrew Yule Finlay +2 more
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