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Angiokeratoma
Known as:
Angiokeratoma [Disease/Finding]
, Angiokeratomas
A vascular lesion in the papillary dermis resulting from ectasia of pre-existing vessels. It is associated with secondary proliferative changes in…
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National Institutes of Health
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Related topics
Related topics
15 relations
Bannayan-Riley-Ruvalcaba Syndrome
Blood supply aspects
Cardiovascular Neoplasm
Cardiovascular system
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
T‐cell‐rich angiomatoid polypoid pseudolymphoma of the skin: a clinicopathologic study of 17 cases and a proposed nomenclature
J. Dayrit
,
Wei-Lien Wang
,
S. Goh
,
P. Ramdial
,
A. Lazar
,
E. Calonje
Journal of cutaneous pathology
2011
Corpus ID: 26165723
Background: We describe a series of previously unreported, distinctive, polypoid solitary T‐cell‐rich cutaneous pseudolymphomas.
Review
2005
Review
2005
Fucosidosis with angiokeratoma. Immunohistochemical & electronmicroscopic study of a new case and literature review
Jean C Kanitakis
,
C. Allombert
,
+4 authors
A. Claudy
Journal of cutaneous pathology
2005
Corpus ID: 38853870
Fucosidosis is a rare lysosomal storage disease due to α‐L‐fucosidase deficiency. It presents clinically with neurological…
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2005
2005
Angiokeratoma Circumscriptum Naeviforme: Successful Treatment with Carbon‐Dioxide Laser Vaporization
J. Pozo
,
E. Fonseca
Dermatologic Surgery
2005
Corpus ID: 30793774
BACKGROUND Angiokeratoma circumscriptum naeviforme (ACN) is an unusual type of localized angiokeratoma that occurs more…
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2002
2002
Acral pseudolymphomatous angiokeratoma of children: immunohistochemical and clonal analyses of the infiltrating cells
Y. Hagari
,
S. Hagari
,
N. Kambe
,
T. Kawaguchi
,
S. Nakamoto
,
M. Mihara
Journal of cutaneous pathology
2002
Corpus ID: 26259794
Background: Acral pseudolymphomatous angiokeratoma of children (APACHE) is a disorder characterized clinically by red nodules…
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1995
1995
Successful treatment of painful crises of Fabry disease with low dose morphine.
Kevin E. Gordon
,
Mark Ludman
,
G.Allen Finle
Pediatric Neurology
1995
Corpus ID: 38543213
1994
1994
alpha-N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosis.
J. de Jong
,
C. Van den Berg
,
+5 authors
R. Wevers
Jornal de Pediatria
1994
Corpus ID: 24933844
1993
1993
Angiokeratoma Corporis Diffusum With Glycopeptiduria due to Deficient Lysosomal a-N-Acetylgalactosaminidase Activity: Clinical, Morphologic, and Biochemical Studies
T. Kanzaki
,
M. Yokota
,
F. Irie
,
Y. Hirabayashi
,
Anne M. Wang
,
R. Desnick
1993
Corpus ID: 71759197
• Background.— Angiokeratoma corporis diffusum is a prominent cutaneous feature of certain lysosomal storage diseases. In this…
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Review
1988
Review
1988
Angiokeratoma circumscriptum: successful treatment with the argon laser.
Krystyna A. Pasyk
,
Louis C. Argenta
,
E. Schelbert
Annals of Plastic Surgery
1988
Corpus ID: 27774027
This article describes 2 patients with angiokeratoma circumscriptum for whom the argon laser proved to be a highly successful…
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1981
1981
Thrombotic angiokeratoma circumscriptum simulating melanoma.
L. Goldman
,
S. H. Gibson
,
D. Richfield
Archives of Dermatology
1981
Corpus ID: 36938035
Three patients with solitary angiokeratomas, two of the circumscribed type (Fabry) and one of the Mibelli type, are described to…
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Highly Cited
1971
Highly Cited
1971
Ceramide trihexosidosis (fabry's disease) without skin lesions.
J. Clarke
,
J. Knaack
,
J. Crawhall
,
L. Wolfe
New England Journal of Medicine
1971
Corpus ID: 45794454
Abstract Histologic, histochemical and electron microscopical studies of kidney tissue taken by open biopsy from two unrelated…
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