By Siba P. Dubey, Bernhard Schick
This publication presents a complete updated assessment of stripling angiofibroma, with contributions from all proper specialties. beginning with a quick creation to the heritage, etiology and correct anatomy, the e-book is going directly to talk about the pathology, scientific beneficial properties and therapy of this disorder extensive, concluding with a precis of present controversies.
Juvenile Angiofibroma is geared toward an international viewers of otolaryngologists, endoscopists, head and neck surgeons, maxillofacial surgeons, pathologists, radiologists and geneticists.
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Additional resources for Juvenile Angiofibroma
The reason for it is explained in Chap. 3. 1 % in the third decade of life; the youngest patient was 6 years and oldest 32 years old. The largest number of patients was at 13 years in our series. The duration and volume of blood loss during epistaxis apparently reduce as the volume of the tumor increases; the explanation of it is given in Chap. 3. Younger patients with smaller tumors used to bleed severely and the hemoglobin level may go as low as 6 gm%, and blood transfusion at this stage to raise the hemoglobin level may lead to continued bleeding.
19. Angiofibroma: treatment trends in 150 patients during 40 years. Laryngoscope. 1986;96:1321–9. Recurrence and its avoidance in juvenile angiofibroma. Laryngoscope. 2001;111:1509–11. Chapter 4 Recent Concept of Etiology Bernhard Schick Abstract The etiology of the juvenile angiofibroma (JA) has been a mystery for a long time. The numerous etiologies postulated over the years could not find general acceptance being mostly able to explain only one of the specific features of the tumor. The most recent concept regarding the origin of this tumor offers for the first time an explanation that covers all specific features of this tumor and is being supported by detailed molecular studies.
Chapter 4 Recent Concept of Etiology Bernhard Schick Abstract The etiology of the juvenile angiofibroma (JA) has been a mystery for a long time. The numerous etiologies postulated over the years could not find general acceptance being mostly able to explain only one of the specific features of the tumor. The most recent concept regarding the origin of this tumor offers for the first time an explanation that covers all specific features of this tumor and is being supported by detailed molecular studies.