Angioma, hemangioma, kaposi sarcoma, angiokeratoma
- 1 Description
- 2 Occurrences
- 3 Related files (images / graphics)
- 4 Angioma/Hemangioma
- 5 Angiokeratoma 
- 6 Pyogenic granuloma (lobular capillary hemangioma) 
- 7 OTHER VASCULAR TUMORS:
No page uses angioma, hemangioma, kaposi sarcoma, angiokeratoma as keyword.
Related files (images / graphics)
No file uses angioma, hemangioma, kaposi sarcoma, angiokeratoma as keyword.
The most common vascular lesions in childhood are the hemangiomas of infancy and, in adulthood, the cherry angiomas. Hemangiomas and angiomas are benign proliferations of blood vessels.
- Absence of melanocytic criteria
- Lacunae (also known as lagoons): well-demarcated, round to oval red, reddish-brown or reddish-blue areas that commonly vary in size and color within a given lesion. Lacunae may be either tightly clustered or loosely scattered throughout the lesion and they are often located on a background of red, red-blue, or red-white homogeneous color. No vascular structures are seen inside the lacunae.
- Occasionally, individual dilated blood vessels or a red network of vessels may be visible.
- Hemangiomas may develop a partial thrombosis, acquiring a focal blue-black color, or a total thrombosis manifesting a jet-black color.
Angiokeratomas are acquired vascular lesions that present as shiny, soft, dark red to violaceous, 2–10 mm papules which may develop a blue-violaceous to black color and a surface scale. Four clinical subtypes of angiokeratomas have been described: solitary angiokeratoma (the most common type), angiokeratoma of Mibelli, angiokeratoma of Fordyce, and angiokeratoma corporis diffusum.
- Dark lacunae: sharply demarcated, ovoid structures with a dark blue, dark violaceous or black color.
- Blue-White veil: confluent blue pigmentation with an overlying whitish haze.
- Ulceration and surface scale may be present.
- Rarely, rainbow pattern may be present.
Pyogenic granuloma (lobular capillary hemangioma) 
Common, benign, acquired, vascular lesion of the skin and mucosa. Typically presents in children or young adults as a solitary, rapidly growing, red papule or nodule that tends to ulceration and bleeding. They are related to infective organisms, penetrating injury, hormonal factors (pregnancy), retinoid therapy, or other systemic medications (i.e., docetaxel).
- Reddish or red-whitish homogeneous area: a structureless zone whose color varies from completely red to red with whitish zones.
- White collarette: a ring-shaped or arcuate squamous structure that is usually located at the periphery of the lesions.
- White rail lines: white streaks that intersect the lesion.
- Vascular structures (dotted vessels, hairpin vessels, linear-irregular vessels, telangiectasias, polymorphous vessels).
- Ulceration may be present
The most frequent dermoscopic pattern of pyogenic granuloma consists of reddish homogenous areas separated by white lines resembling rails and surrounded by a white collarette.
OTHER VASCULAR TUMORS:
Microvenular hemangioma 
Acquired, slowly growing, asymptomatic, benign vascular tumor that usually presents on the upper limbs, forearms, or trunk of young to middle-aged adults. It appears as sharply circumscribed, bright red, solitary lesions varying in size from 0.5 to 2 cm.
- Diffuse erythema with multiple well-demarcated small red globules of different sizes.
- Peripheral fine pigment network
Angioma serpiginosum 
Benign vascular disorder, characterized clinically by multiple minute, red-to-purple, grouped macules distributed in a serpiginous or gyrate pattern.
- Numerous small, relatively well demarcated, round-to-oval red lacunae
Capillary malformation that is present at birth and persists throughout life. It may be localized or cover extensive areas of the skin surface.
Superficial port-wine stain:
- Red dotted and globular vessels
Deep port-wine stain:
- Dilated linear and tortuous vessels
- Gray-whitish veil
- Pale circular areas surrounding a central brownish dot
- Dermoscopic characteristics from either superficial and deep port-wine stain
Lymphangioma circumscriptum 
Malformation involving primarily lymphatic vessels. Clinically, it appears as numerous small vesicle-like lesions grouped in a plaque.
Lacunar pattern composed of :
- Clear to tan lacunae surrounded by pale septa if there is no inclusion of blood in the lacunae
- Yellow to pink lacunae alternating with dark red or bluish lacunae, if there is inclusion of blood in the lacunae
- Hypopyon-like feature (half and half blIster): a sign observed when the blood inside the lacunae accumulates in the lowest part of the lacunae due to sedimentation, resembling the appearance of the hypopion in the eye
Targetoid hemosiderotic hemangioma (hobnail hemangioma) 
Uncommon, benign, solitary, vascular lesion of lymphatic origin. The classic clinical presentation is as single, annular, targetoid-appearance vascular lesion with a brown to violaceous central papule surrounded by a thin, pale area and a peripheral ecchymotic ring. Patients usually describe cyclic changes in their lesions. Dermoscopy
- Central area with red and dark lacunae
- Peripheral circular reddish-violaceous homogeneous area
- Sometimes, intermediate skin-coloured, yellow or white circular homogeneous area.
- Occasionally, a reddish-violaceous or ecchymotic homogeneous area occupies the whole lesion.
- A peripheral delicate pigment network, white structures (shiny white lines) may be present.
Vascular proliferation caused by human herpesvirus-8 (HHV-8). It is considered a low-grade malignant vascular tumor. There are four recognized clinical subsets of Kaposi’s sarcoma: classic, endemic, iatrogenic, and HIV related. Clinically the cutaneous lesions begin as reddish-blue macules or plaques that gradually enlarge and become nodular.
- Homogeneous pattern with differing colors (i.e., whitish, pinkish, reddish, bluish, or violaceous) in different lesions in the same patient.
- Rainbow-like appearance: multicolored areas showing various colors of the rainbow spectrum. This sign is not pathognomonic of Kaposi’s sarcoma and it is only seen with polarized light dermoscopy.
- Whitish structureless areas, vascular structures, scale, and a white collarette may also be seen.
Aggressive neoplasm which is mainly divided into three variants: angiosarcoma of the head and scalp, lymphoedema-associated angiosarcoma and radiation-induced angiosarcoma. It is characterized by a tendency to metastasize to regional lymph nodes and lungs. Prognosis is poor. Clinically, early lesions develop as ill-defined violaceous to bluish areas with an indurated border and advanced lesions become elevated or nodular and occasionally ulcerated.
- Homogeneous pattern with combinations of colors (i.e., whitish, pinkish, reddish, bluish, or violaceous)
- White lines at the nodular parts.
- Zaballos et al.: Dermoscopy of solitary angiokeratomas: a morphological study. Arch Dermatol 2007;143:318-25. PMID: 17372096. DOI.
- Zaballos et al.: Dermoscopy of pyogenic granuloma: a morphological study. Br. J. Dermatol. 2010;163:1229-37. PMID: 20846306. DOI.
- Scalvenzi et al.: Dermoscopy of microvenular hemangioma: report of a case. Dermatology (Basel) 2007;215:69-71. PMID: 17587844. DOI.
- Ohnishi et al.: Angioma serpiginosum: a report of 2 cases identified using epiluminescence microscopy. Arch Dermatol 1999;135:1366-8. PMID: 10566835.
- Piccolo et al.: Dermatoscopy of Vascular Lesions. Dermatol Clin 2018;36:389-395. PMID: 30201148. DOI.
- Gencoglan et al.: Hypopyon-like features: new dermoscopic criteria in the differential diagnosis of cutaneous lymphangioma circumscriptum and haemangiomas?. J Eur Acad Dermatol Venereol 2012;26:1023-5. PMID: 21645121. DOI.
- Zaballos et al.: Dermoscopy of Targetoid Hemosiderotic Hemangioma: A Morphological Study of 35 Cases. Dermatology (Basel) 2015;231:339-44. PMID: 26458032. DOI.
- Cheng et al.: Rainbow pattern in Kaposi's sarcoma under polarized dermoscopy: a dermoscopic pathological study. Br. J. Dermatol. 2009;160:801-9. PMID: 19067686. DOI.
- Vázquez-López et al.: Dermoscopic rainbow pattern in non-Kaposi sarcoma lesions. Br. J. Dermatol. 2009;161:474-5. PMID: 19438855. DOI.
- Zalaudek et al.: Clinical, dermoscopic and histopathological features of spontaneous scalp or face and radiotherapy-induced angiosarcoma. Australas. J. Dermatol. 2013;54:201-7. PMID: 22943153. DOI.