2022
DOI: 10.1016/j.websem.2022.100731
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The International Society for the Study of Vascular Anomalies (ISSVA) ontology

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Cited by 5 publications
(5 citation statements)
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“…At present, the classification of hemangiomas in animals is unclear, as well as the definition of each tumor subtype. The latest International Society for the Study of Vascular Anomalies (ISSVA) guideline classifies human benign hemangiomas as infantile hemangiomas, congenital hemangiomas, tufted hemangiomas, spindle cell hemangiomas, epithelioid hemangiomas, pyogenic hemangiomas, micro capillary hemangiomas and others [ 16 ]. In general, infant hemangiomas begin to grow at 2–3 weeks after birth, with 40 times more proliferating endothelial cells and mast cells in the tumor than in normal tissue.…”
Section: Discussionmentioning
confidence: 99%
“…At present, the classification of hemangiomas in animals is unclear, as well as the definition of each tumor subtype. The latest International Society for the Study of Vascular Anomalies (ISSVA) guideline classifies human benign hemangiomas as infantile hemangiomas, congenital hemangiomas, tufted hemangiomas, spindle cell hemangiomas, epithelioid hemangiomas, pyogenic hemangiomas, micro capillary hemangiomas and others [ 16 ]. In general, infant hemangiomas begin to grow at 2–3 weeks after birth, with 40 times more proliferating endothelial cells and mast cells in the tumor than in normal tissue.…”
Section: Discussionmentioning
confidence: 99%
“…Hemangioma of the conjunctiva and eye lid is evident clinically as congenital anomalies on rare occasions 1–6 . Recently, hemangioma and lymphangioma are all together designated as vascular malformations in the entity of vascular anomalies which contain the other sub‐entity of vascular tumors, according to the International Society for the Study of Vascular Anomalies (ISSVA) classification 7,8 . Vascular tumors show proliferative changes of vascular endothelial cells while vascular malformations consist of structural vascular abnormalities.…”
Section: Introductionmentioning
confidence: 99%
“… 1 , 2 , 3 , 4 , 5 , 6 Recently, hemangioma and lymphangioma are all together designated as vascular malformations in the entity of vascular anomalies which contain the other sub‐entity of vascular tumors, according to the International Society for the Study of Vascular Anomalies (ISSVA) classification. 7 , 8 Vascular tumors show proliferative changes of vascular endothelial cells while vascular malformations consist of structural vascular abnormalities. Based on the structural components of capillary blood vessels or veins, capillary and cavernous hemangioma are capillary and venous malformations, respectively.…”
Section: Introductionmentioning
confidence: 99%
“…The most recent classification accepted by the International Society for the Study of Vascular Anomalies 2018 (ISSVA) classifies vascular anomalies into vascular tumors and vascular malformations. Vascular malformations can be subdivided into capillary malformations, lymphatic malformations (LM), venous malformations, arteriovenous malformations, and arteriovenous fistulas [ 2 ].…”
Section: Introductionmentioning
confidence: 99%
“…Various classifications have been proposed for lymphangioma: (a) Landing and Farber classified LM into lymphangioma simplex, cavernous lymphangioma, and cystic lymphangioma/hygroma [ 5 ]; (b) based on the depth and size of abnormal lymphatic vessels, LM can be classified into superficial (lymphangioma circumscriptum) and deep (cavernous lymphangioma and cystic hygromas); (c) based on the onset, LM is divided into congenital (more common) and acquired; (d) based on the spread into anatomical spaces in the head and neck region [ 6 ], cystic hygroma can be divided into class/grade I - unilateral infrahyoid, class/grade II - unilateral suprahyoid, class/grade III - unilateral infra and suprahyoid, class/grade IV - bilateral suprahyoid and class/grade V - bilateral infra and suprahyoid [ 7 ]; (e) recently, ISSVA classifies LM into common (cystic) LM (macrocystic LM, microcystic LM, and mixed cystic LM), generalized lymphatic anomaly (GLA), Gorham-Stout disease, channel type LM, and "acquired" progressive lymphatic anomaly [ 2 ].…”
Section: Introductionmentioning
confidence: 99%