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Titlebook: Congenital Vascular Malformations; A Comprehensive Revi Young-Wook Kim,Byung-Boong Lee,Young-Soo Do Book 2017 Springer-Verlag Berlin Heidel

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21#
發(fā)表于 2025-3-25 04:23:09 | 只看該作者
22#
發(fā)表于 2025-3-25 09:45:23 | 只看該作者
Masakazu Umezawa,Karina Nigoghossianmphatics, or any combination of these vascular channels. Characteristically, these lesions “grow in parallel with the growth of the patient.” However, there are certain scenarios in which the vascular malformation can be “aggravated,” generating unwanted symptoms and potential complications. Incitin
23#
發(fā)表于 2025-3-25 13:08:43 | 只看該作者
24#
發(fā)表于 2025-3-25 19:44:31 | 只看該作者
https://doi.org/10.1007/978-3-031-12145-6arifying this misinformation is a comprehension of the categorization of diagnoses. Throughout many years, classification schemas have evolved. Since the 1980s, resulting from Mulliken’s insight, it has been generally accepted that the partition of vascular anomalies into those that proliferate (“tu
25#
發(fā)表于 2025-3-25 23:46:49 | 只看該作者
Business Operations Transparency, through decades. Unfortunately even until today in many places, the differentiation of hemangiomas and vascular malformations is not precisely known or is not accurately used in daily clinical practice. A fundamental statement was the clear differentiation of vascular tumors and vascular malformati
26#
發(fā)表于 2025-3-26 03:34:28 | 只看該作者
27#
發(fā)表于 2025-3-26 05:39:12 | 只看該作者
28#
發(fā)表于 2025-3-26 08:55:55 | 只看該作者
29#
發(fā)表于 2025-3-26 15:17:35 | 只看該作者
https://doi.org/10.1007/978-3-030-63621-0ultifactorial process, studies evaluating response to medical therapies, the identification of genomic and somatic mutations in some patients with vascular anomalies, and other research findings have contributed to our understanding of the pathogenesis of these disorders. Patients with vascular anom
30#
發(fā)表于 2025-3-26 17:48:10 | 只看該作者
Margarida Lima Rego,Diogo Costa Seixasith the conducting veins to diffuse lesions involving all of the venous structures in multiple planes of an involved anatomic area. The genetic basis is fairly well understood. Clinical problems include pain, deformity, bleeding, and consumption coagulopathy. VMs are hyperintense on T2-weighted MRI
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