Results 101 to 110 of about 801 (144)
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Pediatrics, 1971
I have read with interest the article of Dr. D. C. Mauger on Letterer-Siwe's disease complicated with intravascular coagulation (Pediatrics, 47: 435, 1971). I think that the possibility of intravascular coagulation has not been proven conclusively in the absence of measurement of some key factors, especially with the degree of hepatosplenomegaly this ...
R, Lopez, D C, Mauger
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I have read with interest the article of Dr. D. C. Mauger on Letterer-Siwe's disease complicated with intravascular coagulation (Pediatrics, 47: 435, 1971). I think that the possibility of intravascular coagulation has not been proven conclusively in the absence of measurement of some key factors, especially with the degree of hepatosplenomegaly this ...
R, Lopez, D C, Mauger
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DAUNOMYCIN IN LETTERER-SIWE'S DISEASE
Lancet, The, 1968G, Segni, R, Mastrangelo, G, Tortorolo
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Archives of Dermatology, 1949
In 1924 Letterer 1 described a disease characterized by enlargement of the spleen and the liver, associated with anemia and a purpuric eruption. The patient in Letterer's case was an infant 6 months old, who died within four days after admission to the hospital.
S E, SWEITZER, C W, LAYMON
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In 1924 Letterer 1 described a disease characterized by enlargement of the spleen and the liver, associated with anemia and a purpuric eruption. The patient in Letterer's case was an infant 6 months old, who died within four days after admission to the hospital.
S E, SWEITZER, C W, LAYMON
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Letterer-siwe disease in adults
Cancer, 1989Histiocytosis X (HX) is a rare disorder of histiocytic proliferation characterized by a broad spectrum of clinicopathologic disease. An unusual case of Letterer-Siwe disease (LSD) or subacute disseminated HX in a 71-year-old woman is presented. The patient had a 3-year history of splenomegaly before skin lesions developed.
F M, Novice +5 more
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Letterer-Siwe disease in an octogenarian
Journal of the American Academy of Dermatology, 1984The case of an 81-year-old woman suffering for about 1 year from a typical form of Letterer-Siwe disease (LSD) is reported. The only important systemic involvement was hepatosplenomegaly. The patient was treated with steroids and vinblastine and then with thymopoietin pentapeptide.
R, Caputo +4 more
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Cutaneous Letterer-Siwe Disease
Archives of Pediatrics & Adolescent Medicine, 1969Letterer-Siwedisease is a nonlipid reticuloendotheliosis of unknown etiology and is usually grouped with Hand-Schuller-Christian disease and eosinophilic granuloma as components of histiocytosis X. 1 It typically occurs in infancy and, clinically, is the most generalized and serious of these conditions.
N B, Esterly, H M, Swick
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Congenital Letterer-Siwe Disease
Beiträge zur Pathologie, 1974Summary An acute fulminating case of Letterer-Siwe disease in a newborn female is reported. The infant died 11 days after birth. Autopsy findings revealed advanced Letterer-Siwe disease indicating that the illness had its origin during intrauterine life.
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The American Journal of Digestive Diseases, 1964
A case is presented of a patient with Letterer-Siwe disease who manifested features of primary liver disease upon admission. A brief review of the reticuloendothelioses is also given.
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A case is presented of a patient with Letterer-Siwe disease who manifested features of primary liver disease upon admission. A brief review of the reticuloendothelioses is also given.
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British Journal of Tuberculosis and Diseases of the Chest, 1955
G.A. Barter, J.P. Gorridan, J.W. Magner
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G.A. Barter, J.P. Gorridan, J.W. Magner
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