Abstract
The rarity of lethal midline granuloma and lack of knowledge by the majority of clinicians about this disease makes this disease a difficult entity to diagnose. Nonspecific symptoms of this disease present obstacles in correct diagnosis and lead to a delay in proper treatment. Surgeons play a limited role in this condition. We present a case report of a 38-year-old man with this rare condition.
Original language | English |
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Pages (from-to) | 131-133 |
Number of pages | 3 |
Journal | Egyptian Journal of Otolaryngology |
Volume | 33 |
Issue number | 1 |
DOIs | |
Publication status | Published - Jan 2017 |
Externally published | Yes |
Keywords
- T-cell lymphoproliferative disorder
- lethal midline granuloma
- lymphoma