1980
DOI: 10.1002/mpo.2950080208
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Eosinophilic Granuloma of Bone

Abstract: Eosinophilic granuloma of bone is an uncommon granulomatous process for which therapy recommendations vary considerably. Consequently, a survey of the world literature from 1940 to 1974 was undertaken in an attempt to develop more concrete guidelines. This survey revealed that the disease manifests itself primarily in males under 20 years of age of all races. The most common symptom is pain, with or without swelling. Multiple sites in a single case are frequent. The clinical course is generally benign, unlike … Show more

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Cited by 116 publications
(45 citation statements)
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“…Surgical curettage has been recommended for those lesions in accessible areas. Although aggressive surgical curettage should be performed, total removal of the lesion has not always been necessary for a favorable response [19]. The use of an ultrasonic surgical aspirator in the extirpation of an EG of the mandible can be useful in avoiding major nerves and vessels [20].…”
Section: Discussionmentioning
confidence: 99%
“…Surgical curettage has been recommended for those lesions in accessible areas. Although aggressive surgical curettage should be performed, total removal of the lesion has not always been necessary for a favorable response [19]. The use of an ultrasonic surgical aspirator in the extirpation of an EG of the mandible can be useful in avoiding major nerves and vessels [20].…”
Section: Discussionmentioning
confidence: 99%
“…Conventional imaging modalities such as skeletal surveys and technician bone scans have been the standard methods of determining sites of Langerhans cell histiocytosis (LCH) in the bones [1,2]. Reports comparing the sensitivity of bone scans versus skeletal surveys have conflicting views on which modality is best [3].…”
Section: Introductionmentioning
confidence: 99%
“…Usually, eosinophilic granuloma has either unifocal or multifocal lesions; Hand-SchĂŒller-Christian disease is a subset of multifocal eosinophilic granuloma with a triad of signs (lytic skull lesions, exophthalmos and diabetes insipidus); Letterer-Siwe disease is a more fulminate systemic histiocytosis, primarily involving soft tissue sites, such as malignant lymphoma of infancy [1]. Slater and Swarm [3]reported that the skull was the most common site of eosinophilic granuloma (43%). The femur is the next most common site.…”
Section: Introductionmentioning
confidence: 99%