| Literature DB >> 6486324 |
I Janecka, E Housepian, S Trokel, R Rankow, I Jones, F Jakobiec.
Abstract
Malignant lacrimal gland tumors are rare but serious and life-threatening neoplasms. Patients frequently present with symptoms of less than 1 year duration, often demonstrating rapid change during the 6 months preceding diagnosis. Pain and periorbital sensory changes are also reported by patients. Radiographically, bone destruction is a strong indication of a lacrimal gland malignancy as is ophthalmoplegia. Radical three-dimensional resection utilizing a cranioorbital approach offers the best chance for total tumor removal. Immediate reconstruction with a scalp flap is essential for primary healing, as well as esthetic balance of the orbital region.Entities:
Mesh:
Year: 1984 PMID: 6486324 DOI: 10.1016/0002-9610(84)90384-2
Source DB: PubMed Journal: Am J Surg ISSN: 0002-9610 Impact factor: 2.565