Titlebook: Juvenile Angiofibroma; Siba P. Dubey,Bernhard Schick Book 2017 Springer International Publishing Switzerland 2017 Nasopharyngeal Angiofibr

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書目名稱Juvenile Angiofibroma影響因子(影響力)




書目名稱Juvenile Angiofibroma影響因子(影響力)學(xué)科排名




書目名稱Juvenile Angiofibroma網(wǎng)絡(luò)公開度




書目名稱Juvenile Angiofibroma網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Juvenile Angiofibroma被引頻次




書目名稱Juvenile Angiofibroma被引頻次學(xué)科排名




書目名稱Juvenile Angiofibroma年度引用




書目名稱Juvenile Angiofibroma年度引用學(xué)科排名




書目名稱Juvenile Angiofibroma讀者反饋




書目名稱Juvenile Angiofibroma讀者反饋學(xué)科排名

BRAND

Pathologic and Microscopic Featuresvessels. Older lesions tend to be more collagenous and have less vascularity. The growth of the tumor is suggested to be provoked by testosterone stimulation during puberty in males. Only rare cases of transformation into malignancy have been reported.

含糊

Juvenile Angiofibroma and Eyeven blindness. The compressed cavernous sinus could lead to tortuous retinal veins, retinal edema, and palpebral edema. Pressure over oculomotor, trochlear, and abducens nerve could induce paralysis of the corresponding extraocular muscles and presenting as strabismus.

FRAX-tool

衍生

Surgical Anatomy of the Skull Baseratemporal fossa are the main area of interest. Furthermore some embryological considerations are given, concerning the origin of the juvenile angiofibroma, which can be interpreted as a dysontogenetic tumor.

venous-leak

Recent Concept of Etiologyor offers for the first time an explanation that covers all specific features of this tumor and is being supported by detailed molecular studies. Herein, the etiology of JAs as a vascular malformation deriving from remnants of the first branchial arch is demonstrated.

angiography

Noisome

迅速飛過

迷住

the pathology, clinical features and treatment of this disease in depth, concluding with a summary of current controversies.. .Juvenile Angiofibroma. is aimed at a global audience of otolaryngologists, endoscopists, head and neck surgeons, maxillofacial surgeons, pathologists, radiologists and geneticists..978-3-319-45343-9