Clinical Ophthalmic Oncology: Eyelid and Conjunctival Tumors - download pdf or read online

By Bryan R. Costin MD, Julian D. Perry MD (auth.), Jacob Pe'er, Arun D. Singh (eds.)

ISBN-10: 3642383351

ISBN-13: 9783642383359

ISBN-10: 364238336X

ISBN-13: 9783642383366

Written through the world over well known specialists, medical Ophthalmic Oncology offers functional advice and suggestion at the prognosis and administration of the full variety of ocular cancers. The ebook offers the entire state of the art wisdom required so as to determine those cancers early and to regard them as successfully as attainable. utilizing the knowledge supplied, readers should be capable of supply potent sufferer care utilizing the newest wisdom on all elements of ophthalmic oncology, to make sure diagnostic conclusions in keeping with comparability with various full-color scientific photos, and to find required details quick due to the clinically targeted and basic layout. during this quantity, the exam innovations, type, and differential prognosis of eyelid tumors and conjunctival and corneal tumors are conscientiously defined, and treatment plans are thought of in detail.​

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Additional info for Clinical Ophthalmic Oncology: Eyelid and Conjunctival Tumors

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Malignant Transformation Frequent follow-up with dilated fundus examination is required because of a small risk of development of a uveal melanoma [40]. Possibility of malignant transformation of the cutaneous component is even more remote [41]. Treatment Periodic observation including dilated fundus examination is the recommended treatment. 3 Acquired Nevus Acquired nevi develop between the ages of 5 and 10 years. Mild to moderate sun exposure in early life induces the development of nevi [42], and nevus density is highest in the sun-exposed areas [43].

Pediatr Dermatol. 1984;1:295–8. 51. Marghoob AA. The dangers of atypical mole (dysplastic nevus) syndrome. Teaching at-risk patients to protect themselves from melanoma. Postgrad Med. 1999;105:147–8, 151–2, 154 passim. 3 Benign Squamous and Melanocytic Tumors 52. Salopek TG. The dilemma of the dysplastic nevus. Dermatol Clin. 2002;20:617–28. 53. Clark Jr WH, Reimer RR, Greene M, Ainsworth AM, Mastrangelo MJ. Origin of familial malignant melanomas from heritable melanocytic lesions: ‘The B-K Mole syndrome’.

1989;13:931–9. 49. Weedon D. Borderline melanocytic tumors. J Cutan Pathol. 1985;12:266–70. 50. Goldes J, Holmes S, Satz M, Cich J, Dehner L. Melanoma masquerading as Spitz nevus following acute lymphoblastic leukaemia. Pediatr Dermatol. 1984;1:295–8. 51. Marghoob AA. The dangers of atypical mole (dysplastic nevus) syndrome. Teaching at-risk patients to protect themselves from melanoma. Postgrad Med. 1999;105:147–8, 151–2, 154 passim. 3 Benign Squamous and Melanocytic Tumors 52. Salopek TG. The dilemma of the dysplastic nevus.

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Clinical Ophthalmic Oncology: Eyelid and Conjunctival Tumors by Bryan R. Costin MD, Julian D. Perry MD (auth.), Jacob Pe'er, Arun D. Singh (eds.)


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