| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3186166 | Annales de Dermatologie et de Vénéréologie | 2015 | 4 Pages |
Abstract
IGM is a rare disease of unknown aetiology. Diagnosis is based on characteristic histological features and exclusion of other granulomatous diseases. Extra-mammary signs are rare and include erythema nodosum, arthralgia and episcleritis. Management is poorly codified.
Keywords
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Dermatology
Authors
J. Fahmy, M. Halabi-Tawil, M. Bagot, B. Tournant, A. Petit,