Erdheim-Chester disease: a distinct lipoidosis or part of the spectrum of histiocytosis?
Autor: | A C Brower, G F Worsham, A H Dudley |
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Rok vydání: | 1984 |
Předmět: |
Adult
Male Pathology medicine.medical_specialty Tibia business.industry Disease Middle Aged Lipidoses medicine.disease Diagnosis Differential Eosinophilic Granuloma Radiography Histiocytosis Langerhans-Cell Histiocytosis Fibula Histiocytoses Erdheim–Chester disease Humans Medicine Female Radiology Nuclear Medicine and imaging business Osteosclerosis Aged |
Zdroj: | Radiology. 151:35-38 |
ISSN: | 1527-1315 0033-8419 |
DOI: | 10.1148/radiology.151.1.6608118 |
Popis: | Erdheim-Chester disease has always been considered a distinct lipoidosis based on clinical and radiographic criteria. Pathologically, it has been indistinguishable from Hand-Schüller-Christian disease. Analysis of the 15 reported cases lends some doubt as to the diagnostic criteria. A new case is presented that strongly suggests that Erdheim-Chester disease is actually part of the spectrum of the histiocytoses. |
Databáze: | OpenAIRE |
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