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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5204_Библиотеки_им_академика_М_И_Перельмана.pdf
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Index
T
Targetoid hemosiderotic hemangioma, 102,
104, 105
V
Vascular tumors
acquired elastotic hemangioma, 108, 109
AVL, 113–115
classical vasoformative tumors
angiomatosis, 84
angiosarcoma, 91–94
arteriovenous hemangioma, 81–83
benign lymphangioendotheli-
oma, 88, 89
capillary (lobular) hemangioma, 63–65
cavernous hemangioma, 77–79
cavernous lymphangioma, 86–88
cherry (senile) hemangioma, 72–74
congenital hemangioma, 65–68
infantile/juvenile hemangioma, 70–72
intramuscular hemangioma, 83–85
LCA, 89–91
lymphangioma, 86
lymphangiomatosis, 89, 90
microvenular hemangioma, 74–77
classications, 61
composite hemangioendothelioma,
112, 113
diagnosis, 146, 147
EAN, 133–135
EAS, 142–144, 146
EHE, 139–141
epithelioid hemangioma, 131, 132
hobnail hemangioma, 102, 104, 105
immunohistochemical markers, 61, 62
Kaposi sarcoma, 120–125
Kaposiform hemangioendotheli-
oma, 127–129
PHE, 135–137, 139
PILA, 106, 107
reactive lesions
bacillary angiomatosis, 97–101
glomeruloid hemangioma, 100,
102, 103
PEH, 94–97
retiform hemangioendothelioma, 110–112
SCH, 117–120
spindle cell angiosarcoma, 129, 130
vascular malformations, 62
W
Well differentiated liposarcoma (WDLPS), 2
age at presentation, 30
clinical course, 30
denition, 28
differential diagnosis, 31, 32
frequency, 28
immunohistochemistry, 30, 38
inammatory subtype, 30, 35
lipoma-like subtype, 30–32
localization, 30
macroscopy, 30
molecular genetics, 31, 40, 41
prognosis, 31
sclerosing-like subtype, 30, 33, 34
spindle cell subtype, 30, 37