Results 21 to 30 of about 4,096 (231)

Reply to “Lobular capillary hemangioma with halo phenomenon” [PDF]

JAAD Case Reports
Mohammed Ibrahim AlJasser, MBBS
doaj   +2 more sources

Localized palmar angiokeratoma-like lesions following trauma [PDF]

JAAD Case Reports
Alexander J. Jafari, MD, MPH, William Sardinia, BS, Paul Bogner, MD, Drew Kuraitis, MD, PhD   +3 more
doaj   +2 more sources

Multiple giant angiokeratoma of Fordyce on the shaft of the penis masquerading as keratoacanthoma [PDF]

Anais Brasileiros de Dermatologia, 2015
The term 'angiokeratoma' includes a wide range of dermatological conditions of hyperkeratotic vascular disorders with a similar histologic combination of hyperkeratosis and superficial dermal vascular ectasia.
Sudip Kumar Ghosh, Shouvik Ghosh, Megha Agarwal   +2 more
doaj   +1 more source

Solitary Angiokeratoma of the Labial Mucosa: Report of a Rare Case and Literature Review

Dentistry Journal, 2022
Oral angiokeratoma is a rare vascular lesion that has various clinical presentations. It usually occurs as part of generalized angiokeratoma and rarely appears as a solitary lesion with no underlying systemic diseases.
Rahaf M. Alhazmi, Najla Dar-Odeh, Hamzah Babkair   +2 more
doaj   +1 more source

Lobular capillary hemangioma with halo phenomenon [PDF]

JAAD Case Reports
Philip R. Cohen, MD, Nikolas B. Gutierrez, DO, Christof P. Erickson, MD, Antoanella Calame, MD   +3 more
doaj   +2 more sources

Angiokeratoma circumscriptum of children: A case of postinjury with a lesion on the foot

Indian Journal of Paediatric Dermatology, 2020
Angiokeratoma circumscriptum vascular lesions are defined by ectasia of the papillary dermal vessels, and the etiology is unknown. We report a rare case of angiokeratoma circumscriptum following the excision of a lipoma, from the same area, on the right ...
Liuchang Tan, Xinying Li, Yuangang Lu
doaj   +1 more source

Cutaneous manifestations of Fabry disease: A systematic review. [PDF]

J Dermatol
Abstract Fabry disease (FD) is a rare X‐linked lysosomal storage disorder resulting in potential debilitating accumulation of glycosphingolipids in organs such as skin, nerves, heart, kidneys, lungs, and the central nervous system. Skin is easily investigated and can guide clinicians to diagnose FD, minimizing delay of enzyme substitution therapy. This
Al-Chaer RN, Folkmann M, Mårtensson NL, Feldt-Rasmussen U, Mogensen M.   +4 more
europepmc   +2 more sources

Congenital angiokeratoma

Anales de Pediatría (English Edition)
Miguel Mansilla-Polo, Daniel Martín-Torregrosa   +1 more
doaj   +3 more sources

The Continuous Challenge of Diagnosing patients with Fabry disease in Argentina : Genotype, Experiences, Anecdotes, and New Learnings [PDF]

, 2015
The lysosomal storage disorder Fabry disease (FD) is caused by pathogenic mutations in the α-galactosidase A gene, localized in X chromosome. Deficient enzymatic activity of the product of this gene, the lysosomal hydrolase α-galactosidase A, leads to ...
Ceci, Romina, Kisinovsky, Isaac, Roa, Norma, Rozenfeld, Paula Adriana   +3 more
core   +5 more sources

Rare Giant Angiokeratoma of the Vulva: A Case Report

Balkan Medical Journal, 2017
Background: Angiokeratoma of fordyce occurring over on the vulva is a rare condition. Fordyce angiokeratoma is observed more frequently among men than women.
Fatih Doğan, İbrahim Hakan Bucak
doaj   +1 more source