VASCULAIRE MALFORMATIES | ICD10: Q82.5 |
Classificatie van vaatafwijkingen: vasculaire tumoren en vasculaire malformaties: | |
---|---|
Tumoren - infantiele hemangiomen, hemangioma of infancy - snel involuerende congenitale hemangiomen (RICH) - niet-involuerende congenitale hemangiomen (NICH) - gedeeltelijk-involuerende congenitale hemangiomen (PICH) - Kaposiform hemangioendothelioom - overige hemangioendotheliomen - tufted angioma - granuloma pyogenicum |
Malformaties slow-flow - capillair - naevus flammeus (wijnvlek) - ooievaarsbeet (naevus van Unna) - veneus - lymfatisch fast-flow - arterioveneuze malformatie - arterioveneuze fistel - gecombineerde (mixed) malformaties |
Zeldzamere vasculaire malformaties: |
---|
slow-flow - verruceuze veneuze malformaties - glomuveneuze malformaties - generalized lymphatic anomalies - cutis marmorata telangiectatica congenita - phakomatosis pigmentovascularis fast-flow - capillary malformation / arteriovenous malformation syndrome (RASA1) |
Vasculaire malformatie syndromen: |
---|
-
CLOVES syndroom - Klippel-Trenaunay syndroom - Sturge-Weber syndroom - Parkes-Weber syndroom |
naevus flammeus | ooievaarsbeet | teleangiëctasieën |
capillaire malformatie | capillaire malformatie | capillaire malformatie |
veneuze malformatie | veneuze malformatie | veneuze malformatie |
veneuze malformatie | glomuveneuze malformatie | blue rubber bleb nevus |
arterioveneuze malformatie | arterioveneuze malformatie | arterioveneuze malformatie |
arterioveneuze malformatie | arterioveneuze malformatie | arterioveneuze malformatie |
arterioveneuze fistel | arterioveneuze fistel | arterioveneuze fistel |
ISSVA classificatie van vasculaire tumoren: | ||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Benigne vasculaire tumoren - Infantile hemangioma / Hemangioma of infancy - Congenital hemangioma [GNAQ, GNA11] - Rapidly involuting (RICH) - Non-involuting (NICH) - Partially involuting (PICH) - Tufted angioma [GNA14] - Spindle-cell hemangioma [IDH1, IDH2] - Epithelioid hemangioma [FOS] - Pyogenic granuloma (lobular capillary hemangioma) [BRAF, RAS, GNA14] - Overige: - 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 - Related lesions: - Eccrine angiomatous hamartoma - Reactive angioendotheliomatosis - Bacillary angiomatosis Locally aggressive or borderline vascular tumors - Kaposiform hemangioendothelioma [GNA14] - Retiform hemangioendothelioma - Papillary intralymphatic angioendothelioma (PILA), Dabska tumor - Composite hemangioendothelioma - Pseudomyogenic hemangioendothelioma [FOSB] - Polymorphous hemangioendothelioma - Hemangioendothelioma not otherwise specified - Kaposi sarcoma - Overige Malignant vascular tumors - Angiosarcoma [MYC] - Epithelioid hemangioendothelioma [CAMTA1, TFE3] - Overige |
||||||||||||||||||||||||
Simple vascular malformations Capillary malformations (CM) - Nevus simplex / salmon patch, “angel kiss”, “stork bite” - Cutaneous and/or mucosal CM (port-wine stain) - Nonsyndromic CM [GNAQ] - CM with CNS and/or ocular anomalies (Sturge-Weber syndrome) [GNAQ] - CM with bone and/or soft tissues overgrowth [GNA11] - Diffuse CM with overgrowth (DCMO) [GNA11] - CM with melanocytic nevus (phakomatosis pigmentovascularis) [GNAQ56, GNA1156, PTPN1157] - Reticulate CM - CM of MIC-CAP (microcephaly-capillary malformation) [STAMBP] - CM of MCAP (megalencephaly-capillary malformation-polymicrogyria) [PIK3CA] - CM of CM-AVM [RASA1, EPHB4] - Cutis marmorata telangiectatica congenita (CMTC) - Overige - Telangiectasia - Hereditary hemorrhagic telangiectasia (HHT) - HHT1 [ENG], HHT2 [ACVRL1], HHT3, JPHT [SMAD4] - Overige Lymphatic malformations (LM) - Common (cystic) LM [PIK3CA] - Macrocystic LM (cystic hygroma) - Microcystic LM (lymphangioma circuscriptum) - Mixed cystic LM - Generalized lymphatic anomaly (GLA) - Kaposiform lymphangiomatosis (KLA) - LM in Gorham-Stout disease - Channel type LM - Acquired progressive lymphatic anomaly (acquired progressive lymphangioma) - Primary lymphedema (different types) - Nonne-Milroy syndrome [FLT4, VEGFR3] - Primary hereditary lymphedema [VEGFC] - Primary hereditary lymphedema [GJC2, Connexin 47] - Lymphedema-distichiasis syndrome [FOXC2] - Hypotrichosis-lymphedema-telangiectasia [SOX18] - Primary lymphedema with myelodysplasia [GATA2] - Primary generalized lymphatic anomaly (Hennekam lymphangiectasia-lymphedema syndrome) [CCBE1] - Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome [KIF11] - Lymphedema-choanal atresia [PTPN14] - Overige Venous malformations (VM) - Common VM [TEK (TIE2), PIK3CA] - Familial VM cutaneo-mucosal (VMCM) [TEK (TIE2)] - Blue rubber bleb nevus (Bean) syndrome VM [TEK (TIE2)] - Glomuvenous malformation (GVM) [Glomulin] - Cerebral cavernous malformation (CCM) - CCM1 [KRIT1], CCM2 [Malcavernin], CCM3 [PDCD10] - Familial intraosseous vascular malformation (VMOS) [ELMO2] - Verrucous venous malformation (formerly verrucous hemangioma) [MAP3K3] - Overige Arteriovenous malformations (AVM) - Sporadic [MAP2K1] - In HHT (HHT1 [ENG], HHT2 [ACVRL1], HHT3,JPHT [SMAD4]) - In CM-AVM [RASA1, EPHB4] - Overige Arteriovenous fistula (AVF) (congenital) - Sporadic [MAP2K1] - In HHT (HHT1 [ENG], HHT2 [ACVRL1], HHT3,JPHT [SMAD4]) - In CM-AVM [RASA1, EPHB4] - Overige |
||||||||||||||||||||||||
Combined vascular malformations
|
||||||||||||||||||||||||
Anomalies of major named vessels ("channel type" or "truncal"
vascular malformations) Affect: - lymphatics - veins - arteries Anomalies of: - origin - course - number - length - diameter (aplasia, hypoplasia, stenosis, ectasia / aneurysm) - valves - communication (AVF) - persistence (of embryonal vessel) |
||||||||||||||||||||||||
Vascular malformations associated with other anomalies - Klippel-Trenaunay syndrome (CM + VM +/- LM + limb overgrowth) [PIK3CA] - Parkes-Weber syndrome (CM + AVF + limb overgrowth) [RASA1] - Servelle-Martorell syndrome (limb VM + bone undergrowth) - Sturge-Weber syndrome (facial + leptomeningeal CM + eye anomalies +/- bone and/or soft tissue overgrowth) [GNAQ] - Limb CM + congenital non-progressive limb overgrowth [GNA11] - Maffucci syndrome (VM +/- spindle-cell hemangioma + enchondroma) [IDH1, IDH2] - Macrocephaly - CM (M-CM / MCAP) [PIK3CA] - Microcephaly - CM (MICCAP) [STAMBP] - CLOVES syndrome (LM + VM + CM +/- AVM + lipomatous overgrowth) [PIK3CA] - Proteus syndrome (CM, VM and/or LM + asymmetrical somatic overgrowth) [AKT1] - Bannayan-Riley-Ruvalcaba syndroom (AVM + VM + macrocephaly, lipomatous overgrowth) [PTEN] - CLAPO syndrome (lower lip CM + face and neck LM + asymmetry and partial/generalized overgrowth) [PIK3CA] |
||||||||||||||||||||||||
Provisionally unclassified vascular anomalies - Intramuscular hemangioma - Angiokeratoma - Sinusoidal hemangioma - Acral arteriovenous tumor - Multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT) - Cutaneovisceral angiomatosis with thrombocytopenia (CAT) - PTEN (type) hamartoma of soft tissue / "angiomatosis" of soft tissue (PHOST) [PTEN] - Fibro adipose vascular anomaly (FAVA) [PIK3CA] |
1. | ISSVA. ISSVA classification of vascular tumors (2014, 2018). www.issva.org/classification. PDF |
2. | Kunimoto K, Yamamoto Y, Jinnin M. ISSVA Classification of Vascular Anomalies and Molecular Biology. Int J Mol Sci 2022;23(4):2358. |
31-05-2023 (JRM) - www.huidziekten.nl |