Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hannan Javed, M.D.[2]
Overview
Vascular Anomalies
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Vascular Tumors
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Vascular Malformations
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Benign
Locally aggressive or
Borderline
Malignant
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Simple
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Combined°
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of major named vessels
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associated with other anomalies
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Capillary malformations
Lymphatic malformations
Venous malformations
Arteriovenous malformations*
Arteriovenous fistula*
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Capillary venous malformation , Capillary lymphatic malformation
Lymphatic venous malformation, Capillary lymphatic venous malformation
Capillary arteriovenous malformation
Capillary lymphatic arteriovenous malformation
others
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See details
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See list
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° defined as two or more vascular malformations found in one lesion
* high flow lesions
Classification
Classification of Vascular Malformations
| | | | | | | | | | | | | | | | | | | | | | | Vascular malformations | | | | | | | | | | | | | | | | | | | | | |
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| | | | | | | Simple | | | | | | | | Combined | | | | | | | | | | of major named vessels | | | | | | | | asscoiated with other anomalies | | | | | |
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| | | | | | | | | | | | | | | | | | Combined vascular malformations*
CM + VM | Capillary-venous malformation | CVM |
CM + LM | Capillary-lymphatic malformation | CLM |
CM + AVM | Capillary-arteriovenous malformation | CAVM |
LM + VM | Lymphatic-venous malformation | LVM |
CM + LM + VM | Capillary-lymphatic-venous malformation | CLVM |
CM + LM + AVM | Capillary-lymphatic-arteriovenous malformation | CLVM |
CM + VM + AVM | Capillary-venous-arteriovenous malformation | CVAVM |
CM + LM + VM + AVM | Capillary-lymphatic-venous-arteriovenous malformation | CLVAVM |
| | | | | | | | | | Anomalies of major named vessels (also known as "channel type" or "truncal" vascular malformations) | | | | | | | | Vascular malformations associated with other anomalies
Klippel-Trenaunay syndrome | CM + VM +/-LM + limb overgrowth |
Parke's Weber syndrome | CM + AVF + limb overgrowth |
Servelle-Martorell syndrome | Limb VM + bone undergrowth |
Sturge-Weber syndrome | Facial + leptomeningeal CM + eye anomalies
+/-bone and/or soft tissue overgrowth |
Maffucci syndrome | VM +/-spindle-cell hemangioma + enchondroma |
CLOVES syndrome | LM + VM + CM +/-AVM+ lipomatous overgrowth |
Proteus syndrome | CM, VM and/or LM + asymmetrical somatic overgrowth |
Bannayan-Riley-Ruvalcaba sd | lower lip CM + face and neck LM + asymmetry and partial/generalized overgrowth |
Limb CM + congenital non-progressive limb overgrowth | |
Macrocephaly-CM (M-CM / MCAP) | |
Microcephaly-CM (MICCAP) | |
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| | Capillary malformations | | | Lymphatic malformations | | | Venous malformations | | | Arteriovenous malformations | | | Arteriovenous fistula | | | | | | | | | | | | | | | | | | | | | | |
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| | | | Nevus simplex / salmon patch, “angel kiss”, “stork bite” | | | | Common (cystic) LM Macrocystic LM Microcystic LM Mixed cystic LM | | | | Common VM | | | | Sporadic | | | | Sporadic | | | | | | | | | | | | | | | | | | | | | |
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| | | | 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 | | | | | | | | | | | | | | | | | | | | | | |
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| | | | 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 | | | | | | | | | | | | | | | | | | | | | | |
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| | | | CM of CM-AVM | | | | Channel type LM | | | | Glomuvenous malformation (GVM) | | | | Others | | | | Others | | | | | | | | | | | | | | | | | | | | | | |
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| | | | Cutis marmorata telangiectatica congenita (CMTC) | | | | “Acquired” progressive lymphatic anomaly (so called acquired progressive "lymphangioma") | | | | Cerebral cavernous malformation (CCM) | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |
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| | | | Others | | | | Primary lymphedema | | | | Familial intraosseous vascular malformation (VMOS) | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |
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| | | | Telangiectasia Hereditary hemorrhagic telangiectasia (HHT) Others | | | | Others | | | | Verrucous venous malformation (formerly verrucous hemangioma) | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |
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| | | | | | | | | | | | | | Others | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |
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Tables
Anomalies of major named vessels
(also known as "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)
Combined vascular malformations*
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CM + VM
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capillary-venous malformation
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CVM
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CM + LM
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capillary-lymphatic malformation
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CLM
|
CM + AVM
|
capillary-arteriovenous malformation
|
CAVM
|
LM + VM
|
lymphatic-venous malformation
|
LVM
|
CM + LM + VM
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capillary-lymphatic-venous malformation
|
CLVM
|
CM + LM + AVM
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capillary-lymphatic-arteriovenous malformation
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CLAVM
|
CM + VM + AVM
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capillary-venous-arteriovenous malformation
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CVAVM
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CM + LM + VM + AVM
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capillary-lymphatic-venous-arteriovenous m.
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CLVAVM
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Vascular malformations associated with other anomalies
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Klippel-Trenaunay syndrome *
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CM + VM +/-LM + limb overgrowth
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Parkes Weber syndrome
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CM + AVF + limb overgrowth
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Servelle-Martorell syndrome
|
limb VM + bone undergrowth
|
Sturge-Weber syndrome
|
facial + leptomeningeal CM + eye anomalies
+/-bone and/or soft tissue overgrowth
|
Limb CM + congenital non-progressive limb overgrowth
|
|
Maffucci syndrome
|
VM +/-spindle-cell hemangioma + enchondroma
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Macrocephaly-CM (M-CM / MCAP) *
|
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Microcephaly-CM (MICCAP)
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CLOVES syndrome *
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LM + VM + CM +/-AVM+ lipomatous overgrowth
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Proteus syndrome
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CM, VM and/or LM + asymmetrical somatic overgrowth
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Bannayan-Riley-Ruvalcaba sd
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lower lip CM + face and neck LM + asymmetry and partial/generalized overgrowth
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Vascular Tumors
Locally aggressive or borderline vascular tumors
Kaposiform hemangioendothelioma
- Locally Aggressive tumor that originates on skin and occurs primarily in childhood.[1] It is characterized by a single or multiple masses with following characteristics:
** Deep reddish-purple color
** Shiny, firm texture
** Warm to the touch
** Swollen and painful
- May be complicated by Kasabach-Merritt phenomenon (KMP), characterized by consumption coagulopathy, thrombocytopenia, and hemolytic anemia.[2] Typical features also include low fibrinogen and elevated D-dimers.
- Somatic activating GNA14 c.614A>T (p.Gln205Leu) mutations have been found in some KHE.[3]
- Invasion of bone, retroperitoneum, and mediastinum has occured in some cases but no case of metastasis has been reported yet. [4]
- Diagnostic work up may include blood tests, biopsy, contrast enhanced ultrasound and MRI or CT scan imaging.
- Treatment Options include steroid, vincristine, interferon alpha, anti-platelet agents, sirolimus-containing therapies and surgery.[5]
Physiology
Medical Therapy
Naural History
Historical Perspective
References
|
- ↑ C537007
- ↑ D059885
- ↑ 27476652
- ↑ C537007
- ↑ 30054848