Vascular anomalies: Difference between revisions
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{{Family tree | {{Family tree | | | | | | | | | | | | | A01 | | | | | | | | | | | | | | | | | | | | | |A01= Vascular malformations}} | ||
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{{Family tree | {{Family tree | | | B01 | | | | B02 | | | | | B03 | | | | B04 | | | | | |B01=Simple vascular malformations|B02=Combined vascular malformations|B03=Vascular malformations of major named vessels|B04=Vascular malformations asscoiated with other anomalies}} | ||
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{{Family tree | {{Family tree | | | |!| | | | | I02 | | | | | I03 | | | | I04 | | | | | | |I02=Combined vascular malformations* | ||
<table class="wikitable"> | <table class="wikitable"> | ||
<tr><td>'''CM + VM'''</td><td>Capillary-venous malformation</td><td>CVM</td></tr> | <tr><td>'''CM + VM'''</td><td>Capillary-venous malformation</td><td>CVM</td></tr> | ||
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</table> | </table> | ||
|I04=Vascular malformations associated with other anomalies | |I04=Vascular malformations associated with other anomalies | ||
<table class="wikitable"> | |||
<tr><td>'''Klippel-Trenaunay syndrome'''</td><td>CM + VM +/-LM + limb overgrowth</td></tr> | |||
<tr><td>'''Parke's Weber syndrome'''</td><td>CM + AVF + limb overgrowth</td></tr> | |||
<tr><td>'''Servelle-Martorell syndrome'''</td><td>Limb VM + bone undergrowth</td></tr> | |||
<tr><td>'''Sturge-Weber syndrome'''</td><td>Facial + leptomeningeal CM + eye anomalies | |||
+/-bone and/or soft tissue overgrowth</td></tr> | |||
<tr><td>'''Maffucci syndrome'''</td><td>VM +/-spindle-cell hemangioma + enchondroma</td></tr> | |||
<tr><td>'''CLOVES syndrome'''</td><td>LM + VM + CM +/-AVM+ lipomatous overgrowth</td></tr> | |||
<tr><td>'''Proteus syndrome'''</td><td>CM, VM and/or LM + asymmetrical somatic overgrowth</td></tr> | |||
<tr><td>'''Bannayan-Riley-Ruvalcaba sd'''</td><td>lower lip CM + face and neck LM + asymmetry and partial/generalized overgrowth</td></tr> | |||
<tr><td>'''Limb CM + congenital non-progressive limb overgrowth'''</td><td></td></tr> | |||
<tr><td>'''Macrocephaly-CM (M-CM / MCAP)'''</td><td></td></tr> | |||
<tr><td>'''Microcephaly-CM (MICCAP)'''</td><td></td></tr> | |||
</table> | |||
|}} | |}} | ||
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{{Family tree | | | C01 | | | C02 | | | C03 | | | C04 | | | C05 | | | | | | | | | | | | | | | | | | | | | | |C01=Capillary malformations|C02=Lymphatic malformations|C03=Venous malformations|C04=Arteriovenous malformations|C05=Arteriovenous fistula}} | {{Family tree | | | C01 | | | C02 | | | C03 | | | C04 | | | C05 | | | | | | | | | | | | | | | | | | | | | | |C01=Capillary malformations|C02=Lymphatic malformations|C03=Venous malformations|C04=Arteriovenous malformations|C05=Arteriovenous fistula}} | ||
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{{Family tree | | |)| D01 | |)| E01 | |)| F01 | |)| G01 | |)| H01 | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D01 | |)| E01 | |)| F01 | |)| G01 | |)| H01 | | | | | | | | | | | | | | | | | | | | | |D01=Nevus simplex / salmon patch, “angel kiss”, “stork bite”|E01=Common (cystic) LM <br>Macrocystic LM <br>Microcystic LM <br>Mixed cystic LM|F01=Common VM|G01=Sporadic|H01=Sporadic}} | ||
{{Family tree | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{Family tree | | |)| D02 | |)| E02 | |)| F02 | |)| G02 | |)| H02 | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D02 | |)| E02 | |)| F02 | |)| G02 | |)| H02 | | | | | | | | | | | | | | | | | | | | | |D02=Cutaneous and/or mucosal CM (also known as “port-wine” stain) <br>Nonsyndromic CM <br>CM with CNS and/or ocular anomalies (Sturge-Weber syndrome) <br>CM with bone and/or soft tissues overgrowth <br>Diffuse CM with overgrowth (DCMO)|E02=Generalized lymphatic anomaly (GLA) <br>Kaposiform lymphangiomatosis (KLA)|F02=Familial VM cutaneo-mucosal (VMCM)|G02=In HHT|H02=In HHT|}} | ||
{{Family tree | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |!| | | | |!| | | | |!| | | | |!| | | | |!| | | | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{Family tree | | |)| D03 | |)| E03 | |)| F03 | |)| G03 | |)| H03 | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D03 | |)| E03 | |)| F03 | |)| G03 | |)| H03 | | | | | | | | | | | | | | | | | | | | | |D03=Reticulate CM <br>CM of MIC-CAP (microcephaly-capillary malformation) <br>CM of MCAP (megalencephaly-capillary malformation-polymicrogyria)|E03=LM in Gorham-Stout disease|F03=Blue rubber bleb nevus (Bean) syndrome VM|G03=In CM-AVM|H03=In CM-AVM|}} | ||
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{{Family tree | | |)| D04 | |)| E04 | |)| F04 | |`| G04 | |`| H04 | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D04 | |)| E04 | |)| F04 | |`| G04 | |`| H04 | | | | | | | | | | | | | | | | | | | | | |D04=CM of CM-AVM|E04=Channel type LM|F04=Glomuvenous malformation (GVM)|G04=Others|H04=Others|}} | ||
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{{Family tree | | |)| D05 | |)| E05 | |)| F05 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D05 | |)| E05 | |)| F05 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |D05=Cutis marmorata telangiectatica congenita (CMTC)|E05=“Acquired” progressive lymphatic anomaly (so called acquired progressive "lymphangioma")|F05=Cerebral cavernous malformation (CCM) |}} | ||
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{{Family tree | | |)| D06 | |)| E06 | |)| F06 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |)| D06 | |)| E06 | |)| F06 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |D06=Others|E06=Primary lymphedema |F06=Familial intraosseous vascular malformation (VMOS)|}} | ||
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{{Family tree | | |`| D07 | |`| E07 | |)| F07 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | |`| D07 | |`| E07 | |)| F07 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |D07=Telangiectasia <br>Hereditary hemorrhagic telangiectasia (HHT) <br>Others|E07=Others|F07=Verrucous venous malformation (formerly verrucous hemangioma)|}} | ||
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{{Family tree | | | | | | | | | | | | |`| F08 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | | | | | | | | | | | |`| F08 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |F08=Others|}} | ||
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | {{Family tree | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |}} | ||
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Revision as of 15:25, 24 September 2018
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hannan Javed, M.D.[2], Anmol Pitliya, M.B.B.S. M.D.[3]
Overview
Classification
Classification of Vascular Tumors
Vascular tumors | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Benign | Locally aggressive or borderline | Malignant | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Infantile hemangioma / Hemangioma of infancy | Kaposiform hemangioendothelioma* | Angiosarcoma | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Congenital hemangioma* | Retiform hemangioendothelioma | Epithelioid hemangioendothelioma | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Tufted angioma* | Papillary intralymphatic angioendothelioma (PILA), Dabska tumor | Others | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Spindle-cell hemangioma | Composite hemangioendothelioma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Epithelioid hemangioma | Pseudomyogenic hemangioendothelioma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pyogenic granuloma (also known as lobular capillary hemangioma) | Polymorphous hemangioendothelioma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Others Hobnail hemangioma Microvenular hemangioma Anastomosing hemangioma Glomeruloid hemangioma Papillary hemangioma Intravascular papillary endothelial hyperplasia Cutaneous epithelioid angiomatous nodule Acquired elastotic hemangioma Littoral cell hemangioma of the spleen | Hemangioendothelioma not otherwise specified | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Related lesions Eccrine angiomatous hamartoma Reactive angioendotheliomatosis Bacillary angiomatosis | Kaposi sarcoma | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Others | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
*congenital hemangioma (rapidly involuting type) and tufted angioma may be associated with thrombocytopenia and/or consumptive coagulopathy in some cases. Many experts consider tufted angioma and kaposiform hemangioendothelioma to be part of a spectrum rather than distinct entities
Classification of Vascular Malformations
Vascular malformations | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Simple vascular malformations | Combined vascular malformations | Vascular malformations of major named vessels | Vascular malformations asscoiated with other anomalies | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Combined vascular malformations*
| Anomalies of major named vessels (also known as "channel type" or "truncal" vascular malformations)
| Vascular malformations associated with other anomalies
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Capillary malformations | Lymphatic malformations | Venous malformations | Arteriovenous malformations | Arteriovenous fistula | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Nevus simplex / salmon patch, “angel kiss”, “stork bite” | Common (cystic) LM Macrocystic LM Microcystic LM Mixed cystic LM | Common VM | Sporadic | Sporadic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cutaneous and/or mucosal CM (also known as “port-wine” stain) Nonsyndromic CM CM with CNS and/or ocular anomalies (Sturge-Weber syndrome) CM with bone and/or soft tissues overgrowth Diffuse CM with overgrowth (DCMO) | Generalized lymphatic anomaly (GLA) Kaposiform lymphangiomatosis (KLA) | Familial VM cutaneo-mucosal (VMCM) | In HHT | In HHT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Reticulate CM CM of MIC-CAP (microcephaly-capillary malformation) CM of MCAP (megalencephaly-capillary malformation-polymicrogyria) | LM in Gorham-Stout disease | Blue rubber bleb nevus (Bean) syndrome VM | In CM-AVM | In CM-AVM | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
CM of CM-AVM | Channel type LM | Glomuvenous malformation (GVM) | Others | Others | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cutis marmorata telangiectatica congenita (CMTC) | “Acquired” progressive lymphatic anomaly (so called acquired progressive "lymphangioma") | Cerebral cavernous malformation (CCM) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Others | Primary lymphedema | Familial intraosseous vascular malformation (VMOS) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Telangiectasia Hereditary hemorrhagic telangiectasia (HHT) Others | Others | Verrucous venous malformation (formerly verrucous hemangioma) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Others | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||