Results 81 to 90 of about 223 (112)
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ECCRINE ANGIOMATOUS HAMARTOMA

International Journal of Dermatology, 1994
A g‐year‐old girl was seen at our outpatient department with a 5‐year history of a slowly enlarging hyperpigmented area with increased sweating on the right upper chest and back. There was no history of pain or tenderness over the lesion. She was the second child of a nonconsanguineous marriage.
L V, Nair, A M, Kurien
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Eccrine Angiomatous Hamartoma

The American Journal of Dermatopathology, 2016
Eccrine angiomatous hamartoma (EAH) is a benign cutaneous lesion defined by the proliferation of hamartomatous eccrine and capillary-like vascular elements in the dermis. However, the epidemiologic, morphologic, and histopathologic aspects of this uncommon disorder have yet to be fully delineated.The authors retrospectively reviewed 18 EAH cases ...
Andrew T, Patterson   +5 more
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Eccrine angiomatous hamartoma

International Journal of Dermatology, 1998
A 50‐year‐old Korean man had an erythematous patch on the left side of his chest since birth ( Fig. 1). We first regarded this lesion as nevus flammeus because of the resemblance of the lesion to an erythematous patch that blanched with pressure. Physical examination revealed an 8×5 cm erythematous patch with a central profuse sweating zone surrounded ...
O C, Kwon   +4 more
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Eccrine Angiomatous Hamartoma: A Multiple Variant

Dermatology, 2009
A case of multiple eccrine angiomatous hamartoma present in a boy since birth is reported. Clinically, this condition must be differentiated from other neonatal angiomatoses. Sometimes the clinical findings are nonspecific, whereas histologic examination may exclude angiomatoses with visceral involvement.
Aloi, F   +2 more
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Eccrine angiomatous hamartoma is a lymphatic proliferation

European Journal of Dermatology, 2013
Eccrine angiomatous hamartoma (EAH) is recognized as a vascular hamartoma composed of abnormal proliferation of blood vessels and eccrine glands.We sought to investigate the immunohistochemical results of D2-40 and Prox1 in EAH in order to gain further insight into its histogenesis.We collected 21 cases of EAH diagnosed in a dermatology department ...
Lei, Wang   +3 more
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Eccrine-Pilar Angiomatous Hamartoma

Dermatologica, 2009
A skin lesion consisting of increased numbers of eccrine sweat ducts associated with enveloping angiomatous vascular channels is presented. Although a small number of similar lesions have been described, the present case is unique in that the regional pilar structures were also involved by the periadnexal vascular proliferation.
D.J. Zeller, R.L. Goldman
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Eccrine Angiomatous Hamartoma

Archives of Dermatology, 1989
REPORT OF A CASE A 39-year-old man presented with a 1-month history of pain in a large plaque located over the right foot. Results of a physical examination revealed an otherwise apparently normal, healthy man with a large, red-violaceous plaque over almost the entire right sole, and extending over the lateral side of the foot (Fig 1).
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Eccrine angiomatous hamartoma (nevus):

Journal of Cutaneous Pathology, 1994
Eccrine angiomatous hamartoma (nevus) is a rare form of congenital tumorous malformation with proliferation of eccrine secretory coils and duels, surrounding capillary angiomatous channels and occasionally oilier minor elements. To date, there have been only about 24 cases reported in the literature.
R L, Sulica   +3 more
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Eccrine angiomatous hamartoma causing walking difficulties

Australasian Journal of Dermatology, 2011
ABSTRACTEccrine angiomatous hamartoma (EAH) is a rare tumoral lesion that consists of vascular and eccrine malformation and often occurs in the distal extremities of children. Although EAH is benign, a therapeutic excision may be required for symptomatic or cosmetic considerations.
Shuang, Chen   +5 more
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Enlargement of Eccrine Angiomatous Hamartoma Following Trauma

Pediatric Dermatology, 2015
AbstractEccrine angiomatous hamartoma (EAH) is a rare, benign hamartoma of eccrine and vascular components that predominantly affects children. Growth is typically commensurate with the child's growth. Herein we report an additional case of this rare entity that enlarged after trauma in a 7‐year‐old girl.
Elena B, Hawryluk   +2 more
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