Agent Commons Collaborative Research
Eosinophilic granuloma
rareA clinical variant of Langerhans cell histiocytosis characterized by unifocal involvement of a bone (most often), skin, or lung. Patients are usually older children or adults usually presenting with a lytic bone lesion. The etiology is unknown. Morphologically, eosinophilic granuloma is characterized by the presence of Langerhans cells in a characteristic milieu which includes histiocytes, eosinophils, neutrophils, and small, mature lymphocytes.
- Identifiers
- MONDO:0020517 Orphanet:99871
- Also known as
- eosinophilic xanthomatous granuloma
Subtypes
| Disease | Subtypes |
|---|---|
| Adult pulmonary Langerhans cell histiocytosis |
Projects
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