Cutaneous vascular anomalies. Part I. Hamartomas, malformations, and dilatation of preexisting vessels,☆☆,

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Abstract

Classification of cutaneous vascular anomalies is difficult because conceptual confusion persists between vascular neoplasms and malformations. However, hemangiomas of the infancy fulfill criteria both for hyperplasia and neoplasm because they result from proliferation of endothelial cells, but often undergo complete regression. Despite these pitfalls we have classified cutaneous vascular anomalies into the following categories: hamartomas, malformations, dilatations of preexisting vessels, hyperplasias, benign neoplasms, and malignant neoplasms. In this first part of our clinicopathologic review of vascular anomalies, hamartomas, malformations, and dilatation of preexisting vessels are covered. Hamartomas include several combined vascular and melanocytic proliferations grouped as phakomatosis pigmentovascularis and the so-called eccrine angiomatous hamartoma that consists of proliferations of both eccrine glands and blood vessels. Vascular malformations result from anomalies of embryologic development, and in some of them the abnormalities of the involved vessels are more functional than anatomic, as is the case of nevus anemicus. In contrast, other cutaneous vascular malformations show striking morphologic abnormalities of the vascular structures. These anatomic vascular malformations are subdivided into the following groups: capillary, venous, arterial, lymphatic, and combined anomalies. Spider angioma, capillary aneurysm–venous lake, and telangiectases are not vascular proliferations at all, but dilations of preexisting vessels. In our opinion, most of the lesions described with the generic term of “angiokeratoma” are not authentic vascular neoplasms, but hyperkeratotic malformations of capillaries and venules or acquired telangiectases of preexisting blood vessels of the papillary dermis. Therefore the first group of these “angiokeratomas” are included in the vascular malformations section, and the second group are covered in the section of dilation of preexisting vessels. Lymphangiectases are considered the lymphatic counterpart of angiokeratomas because they result from ectasia of preexisting lymphatic vessels of the papillary dermis. (J Am Acad Dermatol 1997;37:523-49.) Learning objective: At the completion of this learning activity participants should be familiar with vascular abnormalities in terms of classification, clinical characteristics, histopathologic features, differential diagnosis, and treatment. This article provides a comprehensive and updated review of the vascular hamartomas, malformations, and dilatation of preexisting vascular structures.

Section snippets

HAMARTOMAS

Hamartoma refers to a lesion that results from an error in embryologic development and is characterized by an abnormal arrangement of tissues indigenous to an organ.

MALFORMATIONS

Malformation denotes an abnormal structure that resulted from an aberration in embryologic development. Although the term malformation is used conventionally as a synonym for hamartoma, the two are different because hamartoma refers to a miscellaneous collection of tissue elements normally present at a particular site. In some vascular malformations, the abnormalities of the involved vessels are more functional than anatomic, as in the case of nevus anemicus. In contrast, other cutaneous

Spider angioma (nevus araneus)

Spider angioma or nevus araneus is present in 10% to 15% of normal adults and young children. The face, neck, upper part of the trunk, and arm are the regions most frequently involved. In children, spider angioma tends to affect the hands and fingers. 189 A higher incidency is seen in pregnant women and in patients with chronic liver disease. 190 At the end of the pregnancy, the lesions usually disappear without therapy. Clinically, spider angioma is characterized by a central, slightly

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    The CME articles are made possible through an educational grant from the Dermatological Division, Ortho Pharmaceutical Corporation.

    ☆☆

    Reprint requests: Luis Requena, MD, C/Leopoldo Alas Clarin-3°D 28035, Madrid, Spain.

    0190-9622/97/$5.00 + 0 16/2/83992

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