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OCULAR TUMORS
Ocular TumorsDiagnosis & Treatment
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By
Bertil Damato, PhD, FRCS, FRCOphth, Consultant Ophthalmologist, Director St Paul's Eye Unit, Ocular Oncology Centre, Royal Liverpool University Hospital, Liverpool, UK

Description
* Beautifully illustrated in colour with the information presented in a clear and succinct format * The systematic approach covers all aspects of the disease * Provides the trainee and practitioner with a clear and concise account of the management of the most common intraocular tumours

Contents
Preface; INTRODUCTION; Examination techniques: Slit lamp examination; Binocular indirect ophthalmoscopy; Three-mirror examination; Transillumination; Fluorescein angiography; Indocyanine green (ICG) angiography; Ultrasonography; Computerized tomography; Magnetic resonance imaging; Conjunctival imprint cytology; Conjunctival exfoliative cytology; Conjunctival incisional biopsy; Fine needle aspiration biopsy; Uveal incisional biopsy; Uveal excisional biopsy; CONJUNCTIVAL TUMOUR: Melanotic conjunctival lesions: Naevus; Congenital epithelial melanosis; Congenital sub-epithelial melanocytosis; Primary acquired melanosis; Secondary acquired melanosis; Melanoma; Squamous conjunctival tumours: Squamous papilloma; Actinic keratosis; Conjunctival and corneal intra-epithelial neoplasia; Invasive squamous cell carcinoma; Miscellaneous conjunctival tumours: Cysts; Oncocytoma; Sebaceous gland carcinoma; Kaposi sarcoma; Choristomas; Secondary tumours; UVEAL TUMOURS: Naevus: Choroidal naevus; Iris naevus; Melanocytoma; Uveal melanoma: Choroidal melanoma; Ciliary body melanoma; Iris melanoma; Advanced disease; Metastatic disease; Choroidal haemangioma; Choroidal osteoma; Neurofibroma, neurilemmoma and leiomyoma: Neurofibromatosis type 1; Neurofibromatosis type 2; RETINAL TUMOURS: Astrocytic hamartoma; Retinal vascular tumours: Retinal haemangioblastoma; Retinal cavernous angioma; Retinal arteriovenous malformation (racemose angioma); Vasoproliferative tumour; Retinoblastoma: Pathogenesis; Epidemiology; Pathological and clinical features; History; Clinical examination; Systemic investigations; Ocular investigations; Genetic studies; Differential diagnosis; Treatment; Follow-up; Family care; EPITHELIAL TUMOURS: Congenital hypertrophy of the retinal pigment epithelium; Combined hamartoma of the retina and retinal pigment epithelium; Intraocular cysts; Adenoma and adenocarcinoma; Medullopithelioma; SYSTEMIC TUMOURS: Ocular metastasis; Lymphoid tumours: Conjunctival reactive lymphoid hyperplasia; Uveal reactive lymphoid hyperplasia; Conjunctival lymphoma; Primary intraocular lymphoma; Secondary intraocular lymphoma; Hodgkin's lymphoma; Cutaneous T-cell lymphoma; Multiple myeloma; Leukaemia; Paraneoplastic syndromes: Cancer associated retinopathy; Bilateral diffuse uveal melanocytic proliferation; Miscellaneous syndromes; TREATMENT: Radiotherapy: Radiosensitivity; Radioresponsiveness; Brachytherapy; Charged particle radiotherapy; External beam radiotherapy; Stereotactic irradiation; Complications; Surgery: Local resection of conjunctival tumours; Iridectomy; Iridocycletomy; Choroidectomy and cyclochoroidectomy; Endoresection; Enucleation; Exenteration; Phototherapy: Photocoagulation; Transpupillary thermotherapy; Photodynamic therapy; Thermochemotherapy; Complications of phototherapy; Counselling: Communicating with patients; Treatment selection; Psychological problems due to cancer; Psychological problems due to ocular disease; Glossary; Index.

Bibliographic & ordering Information
Paperback, 288 pages, publication date: JUN-2000
ISBN-13: 978-0-7506-2220-2
ISBN-10: 0-7506-2220-2
Imprint: BUTTERWORTH HEINEMANN



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Last update: 25 Aug 2008
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