Results 201 to 210 of about 5,058 (253)
A CASE OF SO-CALLED PSEUDO-MYXOMA PERITONEI, WITH OBSERVATIONS ON THE FORMATION OF HYALIN
, 1893 H. Bettmann
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The American Journal of Dermatopathology, 2021
Abstract: Eosinophilic hyaline inclusions (EHIs) or globules have been reported in various cutaneous tumors including vascular lesions, myoepithelial neoplasms, and basal cell carcinoma. In basal cell carcinoma, the presence of intracytoplasmic inclusions is reportedly associated with myoepithelial differentiation. In this regard, EHI has not
Konstantinos Linos +2 more
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Abstract: Eosinophilic hyaline inclusions (EHIs) or globules have been reported in various cutaneous tumors including vascular lesions, myoepithelial neoplasms, and basal cell carcinoma. In basal cell carcinoma, the presence of intracytoplasmic inclusions is reportedly associated with myoepithelial differentiation. In this regard, EHI has not
Konstantinos Linos +2 more
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Juvenile hyaline Fibromatose [PDF]
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.
C. Hendricks +3 more
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Alcoholic hyalin, microfilaments and microtubules in alcoholic hepatitis.
Acta pathologica et microbiologica Scandinavica. Section A, Pathology, 2009The alcoholic hyalin which is composed of light and dark occasionally swollen and conglomerating filaments, is found to be surrounded by proliferated RER, hypertrophied Golgi apparatus and mitochondria containing enlarged matrical granules.
P. Petersen
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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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Juvenile hyalin fibromatosis as a cause of external nasal obstruction.
The Journal of craniofacial surgery (Print), 2013diagnostic with atypical cells. In our department, excisional biopsy was performed under general anesthesia. After the pathologic report, the patient’s clinical history, and the morphologic findings were evaluated together, the diagnosis is considered to
A. Aytekin, Y. Coban
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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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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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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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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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