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Letterer-Siwe Disease

Known as: Acute histiocytosis X, letterer - siwe disease, ABT-LETTERER-SIWE DISEASE 
A multifocal, multisystem form of Langerhans-cell histiocytosis. There is involvement of multiple organ systems including the bones, skin, liver… Expand
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Pulmonary histiocytosis X is characterized by an accumulation of CD-1-positive histiocytosis X cells in the lung, which also can… Expand
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Highly Cited
2001
Highly Cited
2001
To the Editor: Langerhans'-cell histiocytosis, previously called histiocytosis X, is an accumulation of dendritic Langerhans… Expand
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Highly Cited
2000
Highly Cited
2000
Diminished exercise capacity in advanced pulmonary histiocytosis X does not appear to be related to ventilatory limitation but… Expand
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1996
1996
BACKGROUND: Pulmonary histiocytosis X is a disorder characterised by the presence of destructive granulomas preferentially… Expand
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Highly Cited
1994
Highly Cited
1994
BACKGROUND The lesions of Langerhans'-cell histiocytosis (histiocytosis X), a proliferative histiocytic disorder of unknown cause… Expand
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1991
1991
Sixty-two patients with histiocytosis X were followed for an average of 5 years. The patients were classified into three groups… Expand
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Highly Cited
1989
Highly Cited
1989
Eighteen patients with pulmonary lesions of histiocytosis X were studied with high-resolution computed tomography (CT). Thin… Expand
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Review
1983
Review
1983
The histologic and clinical features of pulmonary histiocytosis X are discussed. The majority of patients are in the third and… Expand
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1973
1973
1. The clinical, radiological and pathological features of 106 cases of eosinophilic granuloma of bone (solitary and multiple… Expand
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