Titlebook: Clinical Ophthalmic Oncology; Retinal Tumors Arun D. Singh,Bertil E. Damato Book 20193rd edition Springer Nature Switzerland AG 2019 Cancer

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書目名稱Clinical Ophthalmic Oncology影響因子(影響力)




書目名稱Clinical Ophthalmic Oncology影響因子(影響力)學(xué)科排名




書目名稱Clinical Ophthalmic Oncology網(wǎng)絡(luò)公開度




書目名稱Clinical Ophthalmic Oncology網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Clinical Ophthalmic Oncology被引頻次




書目名稱Clinical Ophthalmic Oncology被引頻次學(xué)科排名




書目名稱Clinical Ophthalmic Oncology年度引用




書目名稱Clinical Ophthalmic Oncology年度引用學(xué)科排名




書目名稱Clinical Ophthalmic Oncology讀者反饋




書目名稱Clinical Ophthalmic Oncology讀者反饋學(xué)科排名

saturated-fat

,Coats’ Disease,tion for healthy males, and resulted in focal deposition of exudates within the fundus and “peculiar” retinal vascular findings. Four years later, Coats classified his cases of “exudative retinitis” into three groups. Group I manifested massive exudation but no discernable vascular abnormalities. Gr

減少

Retinal Vascular Tumors, retinal arteriovenous communications (Wyburn-Mason syndrome), and retinal vasoproliferative tumor. Retinal vascular tumors can also be considered as congenital or prenatal in origin, maintaining retinal tight junctions and hence not manifesting retinal leakage, such as subretinal fluid or hard exud

Frequency

Retinal Astrocytic Tumors,Retinal astrocytic hamartomas are frequently associated with tuberous sclerosis complex (TSC). “Acquired” retinal astrocytomas develop in somewhat older individuals who have no clinical manifestations of TSC or other systemic syndromes.

變態(tài)

朝圣者

,Tumors of the?Ciliary Epithelium,gnant tumors, the remarkable cellular polymorphism, and the possibility of dealing with either a congenital or acquired tumor. Medulloepithelioma should be considered in the differential diagnosis of a child with leukocoria, especially if there is a gray translucent cystic ciliary body mass, iris ne

朝圣者

Primary Central Nervous System and Retinal Lymphoma,n parenchyma, spinal cord, and leptomeninges. Vitreoretinal lymphoma (VRL) is a variant of PCNSL characterized by ophthalmic involvement. VRL is distinct from other forms of ocular lymphoma that affect the adnexal structures and uveal tract in that the latter are usually low-grade, indolent, B-cell

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