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Items 1 to 67 of about 67
1. Sion-Vardy N, Manor E, Puterman M, Bodner L: Solitary angiokeratoma of the tongue. Med Oral Patol Oral Cir Bucal; 2008 Jan;13(1):E12-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Solitary angiokeratoma of the tongue.
  • Angiokeratoma is a rare cutaneous lesion.
  • It can be either a generalized systemic form, presenting as multiple asymptomatic papules on the skin, associated with metabolic diseases or a solitary cutaneous form.
  • Oral cavity involvement is more common in the systemic form, as a part of a more generalized cutaneous disease, but very rare in the localized form of angiokeratoma.
  • On dermatologic examination, no angiokeratomas were found, anywhere on the skin.
  • The histologic diagnosis was angiokeratoma.
  • A case of a solitary angiokeratoma of the tongue is reported.
  • We report here the third intra-oral case and the second case in the tongue with solitary angiokeratoma.
  • [MeSH-major] Angiokeratoma / pathology. Tongue Neoplasms / pathology

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  • (PMID = 18167473.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
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2. Karen JK, Hale EK, Ma L: Angiokeratoma corporis diffusum (Fabry disease). Dermatol Online J; 2005;11(4):8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma corporis diffusum (Fabry disease).
  • Fabry disease is an x-linked recessive disorder in which deficiency of the lysosomal enzyme alpha-galactosidase A leads to progressive accumulation of globotriaosylceramide in vital organs.
  • [MeSH-major] Fabry Disease / pathology. Skin Diseases, Genetic / pathology
  • [MeSH-minor] Adult. Humans. Male. Skin / pathology

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  • (PMID = 16403380.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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3. Leis-Dosil VM, Alijo-Serrano F, Aviles-Izquierdo JA, Lazaro-Ochaita P, Lecona-Echeverria M: Angiokeratoma of the glans penis: clinical, histopathological and dermoscopic correlation. Dermatol Online J; 2007;13(2):19
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of the glans penis: clinical, histopathological and dermoscopic correlation.
  • Angiokeratoma is a benign vascular lesion characterized by vascular ectasia in the upper dermis and hyperkeratosis.
  • [MeSH-major] Angiokeratoma / pathology. Penis / pathology. Skin Neoplasms / pathology

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  • (PMID = 17498438.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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4. Trickett R, Dowd H: Angiokeratoma of the scrotum: a case of scrotal bleeding. Emerg Med J; 2006 Oct;23(10):e57
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of the scrotum: a case of scrotal bleeding.
  • A 26-year-old man presented to the emergency department after a spontaneous 30 min bleed from his scrotal skin.
  • A diagnosis of angiokeratoma of the scrotum (Fordyce) was made and potential precipitants such as intra-abdominal masses, urinary tract tumours, varicoceles, hernias and angiokeratoma corporis diffusum (Fabry syndrome) were excluded.
  • The important differential diagnoses are angiokeratoma corporis diffusum and malignant melanoma (nodular type).
  • In females, Fordyce angiokeratoma are distributed on labia majora.
  • [MeSH-major] Angiokeratoma / diagnosis. Hemorrhage / etiology. Scrotum. Skin Neoplasms / diagnosis

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  • [Cites] Mil Med. 1994 Jul;159(7):523-4 [7816227.001]
  • [Cites] Arch Dermatol. 2005 Oct;141(10):1325-6 [16230581.001]
  • [Cites] Dermatology. 1996;193(4):275-82 [8993949.001]
  • (PMID = 16988295.001).
  • [ISSN] 1472-0213
  • [Journal-full-title] Emergency medicine journal : EMJ
  • [ISO-abbreviation] Emerg Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2579622
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5. Kudumija B, Mrsić M, Dits S, Matijević V, Thune S, Bozina K: [Classical type of Fabry disease without angiokeratomas--a case report]. Lijec Vjesn; 2007 Dec;129(12):396-400
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  • [Transliterated title] Klasicni oblik Fabryjeve bolesti bez angiokeratoma--prikaz bolesnika.
  • [MeSH-minor] Adult. Angiokeratoma / complications. Humans. Male. Skin Neoplasms / complications

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  • (PMID = 18383742.001).
  • [ISSN] 0024-3477
  • [Journal-full-title] Lijec̆nic̆ki vjesnik
  • [ISO-abbreviation] Lijec Vjesn
  • [Language] hrv
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Croatia
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6. Siponen M, Penna T, Apaja-Sarkkinen M, Palatsi R, Salo T: Solitary angiokeratoma of the tongue. J Oral Pathol Med; 2006 Apr;35(4):252-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Solitary angiokeratoma of the tongue.
  • Angiokeratoma is a rare, cutaneous vascular disorder that can occur in several clinically distinct conditions.
  • It usually presents as multiple, red to blue or black, asymptomatic papules on the skin.
  • We report the second case of a solitary papular angiokeratoma of the oral cavity.
  • [MeSH-major] Angiokeratoma / pathology. Tongue Neoplasms / pathology

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  • (PMID = 16519775.001).
  • [ISSN] 0904-2512
  • [Journal-full-title] Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology
  • [ISO-abbreviation] J. Oral Pathol. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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7. Ulker V, Cakir E, Gedikbasi A, Akyol A, Numanoglu C, Gulkilik A: Angiokeratoma of the clitoris with evident vulvar varicosity. J Obstet Gynaecol Res; 2010 Dec;36(6):1249-51
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of the clitoris with evident vulvar varicosity.
  • We report a case of clitoral angiokeratoma in a 22-year-old nulligravida with a history of surgery to remove a clitoral mass at 6 years of age.
  • [MeSH-major] Angiokeratoma / pathology. Clitoris / pathology. Skin Neoplasms / pathology

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  • [Copyright] © 2010 The Authors. Journal of Obstetrics and Gynaecology Research © 2010 Japan Society of Obstetrics and Gynecology.
  • (PMID = 21040198.001).
  • [ISSN] 1447-0756
  • [Journal-full-title] The journal of obstetrics and gynaecology research
  • [ISO-abbreviation] J. Obstet. Gynaecol. Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
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8. Rees R, Freeman A, Malone P, Garaffa G, Muneer A, Minhas S: Case study: the surgical management of angiokeratoma resulting from radiotherapy for penile cancer. ScientificWorldJournal; 2009;9:339-42
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  • [Title] Case study: the surgical management of angiokeratoma resulting from radiotherapy for penile cancer.
  • Angiokeratoma is a rare, benign skin lesion and a recognised complication of radiation therapy.
  • Here we describe a case of extensive angiokeratoma of the groin and external genitalia resulting from external beam radiation to that area in a patient with penile carcinoma.
  • [MeSH-major] Angiokeratoma / etiology. Radiotherapy / adverse effects. Skin Neoplasms / etiology

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  • (PMID = 19468654.001).
  • [ISSN] 1537-744X
  • [Journal-full-title] TheScientificWorldJournal
  • [ISO-abbreviation] ScientificWorldJournal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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9. Kim Y, Dawes-Higgs E, Mann S, Cook DK: Acral pseudolymphomatous angiokeratoma of children (APACHE). Australas J Dermatol; 2005 Aug;46(3):177-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Acral pseudolymphomatous angiokeratoma of children (APACHE).
  • The histopathology examination revealed a massive subepidermal lymphohistiocytic infiltrate, consistent with acral pseudolymphomatous angiokeratoma of children.
  • [MeSH-major] Angiokeratoma / diagnosis. Pseudolymphoma / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 16008651.001).
  • [ISSN] 0004-8380
  • [Journal-full-title] The Australasian journal of dermatology
  • [ISO-abbreviation] Australas. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Pregnadienediols; 04201GDN4R / Mometasone Furoate
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10. Sierra-Luzuriaga G, Sierra-Montenegro E, Carrillo-Vedova C, Leone-Stay G: [Intergluteal angiokeratoma circumscriptum. Report of one case]. Cir Cir; 2006 Sep-Oct;74(5):373-5
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  • [Title] [Intergluteal angiokeratoma circumscriptum. Report of one case].
  • [Transliterated title] Angioqueratoma circunscrito interglúteo. Reporte de un caso.
  • BACKGROUND: The term angiokeratoma is applied to several diseases with cutaneous vascular lesions.
  • DISCUSSION: Five types of angiokeratomas have been described (angiokeratoma corporis diffusum, angiokeratoma of Mibelli, angiokeratoma of Fordyce, solitary angiokeratoma and angiokeratoma corporal circumscriptum).
  • This patient was identified with an angiokeratoma circumscriptum by pathological and physical characteristics of the tumor.
  • Differential diagnosis is with verrucous hemangioma and the Fabry disease type II (angiokeratoma corporis diffusum).
  • [MeSH-major] Angiokeratoma / surgery. Skin Neoplasms / surgery

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  • (PMID = 17224109.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
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11. Namazi MR, Maghsoodi M: Association of angiokeratoma of the vulva with angioma serpiginosum. J Drugs Dermatol; 2008 Sep;7(9):882-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Association of angiokeratoma of the vulva with angioma serpiginosum.
  • Angioma serpiginosum is a rare benign vascular disorder usually beginning in childhood.
  • Angiokeratoma of the vulva is an uncommon lesion occurring in older women.
  • [MeSH-major] Angiokeratoma / pathology. Hemangioma / pathology. Vulvar Neoplasms / pathology
  • [MeSH-minor] Adult. Buttocks / pathology. Female. Humans. Skin Neoplasms / complications. Skin Neoplasms / pathology

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  • (PMID = 19112804.001).
  • [ISSN] 1545-9616
  • [Journal-full-title] Journal of drugs in dermatology : JDD
  • [ISO-abbreviation] J Drugs Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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12. Malalasekera AP, Goddard JC, Terry TR: Angiokeratoma of Fordyce simulating recurrent penile cancer. Urology; 2007 Mar;69(3):576.e13-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of Fordyce simulating recurrent penile cancer.
  • The histologic examination, however, revealed a benign angiokeratoma with no evidence of recurrent cancer.
  • Angiokeratoma on the scrotum after treatment for carcinoma of the penis has only been documented once.
  • [MeSH-major] Angiokeratoma / diagnosis. Carcinoma, Squamous Cell / diagnosis. Neoplasms, Multiple Primary / diagnosis. Penile Neoplasms / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 17382178.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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13. Luzar B, Neil SM, Calonje E: Angiokeratoma-like changes in extragenital and genital lichen sclerosus. J Cutan Pathol; 2009 May;36(5):540-2

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma-like changes in extragenital and genital lichen sclerosus.
  • They were in close proximity to and even in contact with the overlying epidermis and thus mimicked an angiokeratoma.
  • Angiokeratoma-like changes in lichen sclerosus represent secondary features because of damage to the dermis by lichen sclerosus and are characterized histologically by ectatic thin-walled vascular spaces in the papillary dermis intimately associated with the epidermis.
  • [MeSH-minor] Adolescent. Aged. Angiokeratoma / pathology. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Skin Neoplasms / pathology

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  • (PMID = 19187108.001).
  • [ISSN] 1600-0560
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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14. Weidemann F, Strotmann JM, Breunig F, Niemann M, Maag R, Baron R, Eggert AO, Wanner C: Misleading terms in Anderson-Fabry disease. Eur J Clin Invest; 2008 Mar;38(3):191-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Signs and symptoms of classic Fabry disease manifest itself on the skin (angiokeratoma), the nervous system (acroparaesthesia), the heart (restrictive cardiomyopathy) and a variety of other organs.
  • RESULTS: Among the 47 male and 53 female patients (mean age 41 +/- 16 years) with genetically proven disease, the Fabry-type vascular skin lesions were without hyperkeratotic aspect and keratomas were virtually absent.
  • We propose to replace the term 'angiokeratoma' with 'angioma', the term 'acroparaesthesia' with 'neuropathic pain' and the term 'restrictive cardiomyopathy' with 'cardiac hypertrophic storage disease'.
  • [MeSH-major] Angiokeratoma / diagnosis. Cardiovascular Diseases / diagnosis. Fabry Disease / diagnosis. Paresthesia / diagnosis
  • [MeSH-minor] Adult. Cohort Studies. Diagnosis, Differential. Echocardiography, Doppler. Female. Humans. Male. Middle Aged. Skin Diseases / pathology. Terminology as Topic

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  • (PMID = 18257782.001).
  • [ISSN] 1365-2362
  • [Journal-full-title] European journal of clinical investigation
  • [ISO-abbreviation] Eur. J. Clin. Invest.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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15. Pianezza ML, Singh D, Van der Kwast T, Jarvi K: Rare case of recurrent angiokeratoma of Fordyce on penile shaft. Urology; 2006 Oct;68(4):891.e1-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rare case of recurrent angiokeratoma of Fordyce on penile shaft.
  • Angiokeratomas are benign cutaneous vascular lesions characterized by dilated thin-walled blood vessels lying in the upper part of the dermis, mostly associated with an epidermal reaction such as acanthosis and/or hyperkeratosis.
  • We report a rare case of angiokeratoma of Fordyce located on the shaft of the penis and associated with two recurrences after appropriate surgical excision.
  • [MeSH-major] Angiokeratoma / pathology. Skin Neoplasms / pathology

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  • (PMID = 17070385.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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16. Pavone P, Lucenti C, Fraggetta F, Micali G, Incorpora G, Ruggieri M: Congenital lymphedema-lymphangiectasia associated with scrotal angiokeratoma (Fordyce Type) and hearing impairment. J Clin Gastroenterol; 2008 Jul;42(6):715-9
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  • [Title] Congenital lymphedema-lymphangiectasia associated with scrotal angiokeratoma (Fordyce Type) and hearing impairment.
  • Congenital lymphangiectasia-lymphedema is a rare disorder that presents with edema of the lower half of the body, the face, hands, and scrotum, or with protein-losing enteropathy owing to structural anomalies in the endothelium of the lymphatic system.
  • We describe a biopsy-proven case of severe lymphangiectasia-lymphedema in a 16-year-old boy who was born to consanguineous parents and who, in addition, had mild (20 to 40 dB), early onset, sensorineural deafness and skin abnormalities, consisting of angiokeratomas of the face, hands, and feet, and also a large, localized angiokeratoma of the scrotum and the penis (Fordyce type).
  • To the best of our knowledge, this constellation of lymphatic, skin, hearing, and systemic abnormalities seen in the proband has not been previously reported.
  • [MeSH-major] Angiokeratoma / complications. Hearing Loss, Sensorineural / complications. Lymphangiectasis / complications. Lymphedema / complications
  • [MeSH-minor] Adolescent. Biopsy. Consanguinity. Humans. Male. Penile Neoplasms / complications. Penile Neoplasms / pathology. Scrotum / pathology. Skin Neoplasms / complications. Skin Neoplasms / pathology


17. Lapidoth M, Ad-El D, David M, Azaria R: Treatment of angiokeratoma of Fordyce with pulsed dye laser. Dermatol Surg; 2006 Sep;32(9):1147-50
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  • [Title] Treatment of angiokeratoma of Fordyce with pulsed dye laser.
  • METHODS: Twelve patients with Fitzpatrick skin type II to IV were treated for angiokeratomas of Fordyce with pulsed dye laser (5.5-8.0 J/cm(2)) in two to six sessions.
  • CONCLUSION: Pulsed dye laser is effective and safe for the treatment of angiokeratoma of Fordyce, with minimum side effects, providing an additional nonablative therapeutic option.
  • [MeSH-major] Angiokeratoma / radiotherapy. Genital Neoplasms, Male / radiotherapy. Low-Level Light Therapy / methods. Skin Neoplasms / radiotherapy

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  • (PMID = 16970695.001).
  • [ISSN] 1076-0512
  • [Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
  • [ISO-abbreviation] Dermatol Surg
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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18. Okuyama R, Masu T, Mizuashi M, Watanabe M, Tagami H, Aiba S: Pseudolymphomatous angiokeratoma: report of three cases and an immunohistological study. Clin Exp Dermatol; 2009 Mar;34(2):161-5
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  • [Title] Pseudolymphomatous angiokeratoma: report of three cases and an immunohistological study.
  • BACKGROUND: Pseudolymphomatous angiokeratoma (PA), originally termed 'acral pseudolymphomatous angiokeratoma of children', is a disorder characterized clinically by development of red nodules on the extremities and histologically by a subepidermal dense lymphocyte infiltrate.
  • [MeSH-major] Angiokeratoma / pathology. B-Lymphocytes / pathology. Skin Neoplasms / pathology. T-Lymphocytes / pathology

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  • (PMID = 18681875.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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19. Albano LM, Rivitti C, Bertola DR, Honjo RS, Kelmann SV, Giugliani R, Kim CA: Angiokeratoma: a cutaneous marker of Fabry's disease. Clin Exp Dermatol; 2010 Jul;35(5):505-8
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  • [Title] Angiokeratoma: a cutaneous marker of Fabry's disease.
  • A survey and screening for FD were performed on men with biopsy-proven angiokeratoma and some of their relatives (n = 29).
  • Dermatologists should be aware of this prominent early feature and investigate unexplained cutaneous vascular lesions to detect FD.
  • [MeSH-major] Angiokeratoma / pathology. Fabry Disease / pathology. Skin Neoplasms / pathology

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  • (PMID = 19843083.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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20. Yildirim M, Kilinç N, Oktay MF, Topçu I: A case of solitary angiokeratoma circumscriptum of the tongue. Kulak Burun Bogaz Ihtis Derg; 2007;17(6):333-5
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  • [Title] A case of solitary angiokeratoma circumscriptum of the tongue.
  • Angiokeratoma circumscriptum is an uncommon vascular entity.
  • After an incisional biopsy of the lesion, the diagnosis was made as solitary angiokeratoma circumscriptum.
  • [MeSH-major] Angiokeratoma / diagnosis. Skin Neoplasms / diagnosis. Tongue / pathology

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  • (PMID = 18187999.001).
  • [ISSN] 1300-7475
  • [Journal-full-title] Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat
  • [ISO-abbreviation] Kulak Burun Bogaz Ihtis Derg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Turkey
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21. Bechara FG, Happle R, Altmeyer P, Grabbe S, Jansen T: Angiokeratoma circumscriptum arranged in a systematized band-like pattern suggesting mosaicism. J Dermatol; 2006 Jul;33(7):489-91
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma circumscriptum arranged in a systematized band-like pattern suggesting mosaicism.
  • A hyperkeratotic aspect of the lesional skin surface had developed at the age of 2 years.
  • The clinical and histopathological findings were consistent with a diagnosis of angiokeratoma circumscriptum.
  • The systematized band-like arrangement observed in the present case strongly supports the concept that angiokeratoma circumscriptum reflects a mosaic state of a mutation that is so far unknown.
  • [MeSH-major] Angiokeratoma / pathology. Skin Neoplasms / pathology

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  • (PMID = 16848823.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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22. Oni G, Mahaffey P: Treatment of angiokeratoma of the vulva with pulsed dye laser therapy. J Cosmet Laser Ther; 2010 Feb;12(1):51-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Treatment of angiokeratoma of the vulva with pulsed dye laser therapy.
  • Angiokeratoma of the vulva is relatively rare with few cases reported in the literature.
  • [MeSH-major] Angiokeratoma / radiotherapy. Lasers, Dye. Low-Level Light Therapy / methods. Skin Neoplasms / radiotherapy. Vulva

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  • (PMID = 19929291.001).
  • [ISSN] 1476-4180
  • [Journal-full-title] Journal of cosmetic and laser therapy : official publication of the European Society for Laser Dermatology
  • [ISO-abbreviation] J Cosmet Laser Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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23. Ozdemir M, Baysal I, Engin B, Ozdemir S: Treatment of angiokeratoma of Fordyce with long-pulse neodymium-doped yttrium aluminium garnet laser. Dermatol Surg; 2009 Jan;35(1):92-7
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  • [Title] Treatment of angiokeratoma of Fordyce with long-pulse neodymium-doped yttrium aluminium garnet laser.
  • MATERIALS AND METHODS: Ten consecutive patients with angiokeratoma of Fordyce were treated with long-pulse Nd:YAG laser in two to six sessions.
  • CONCLUSION: The long-pulse Nd:YAG laser is a highly effective and safe treatment for angiokeratoma of Fordyce.
  • [MeSH-major] Angiokeratoma / radiotherapy. Lasers, Solid-State / therapeutic use. Skin Neoplasms / radiotherapy

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  • (PMID = 19076189.001).
  • [ISSN] 1524-4725
  • [Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
  • [ISO-abbreviation] Dermatol Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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24. Yiğiter M, Arda IS, Tosun E, Celik M, Hiçsönmez A: Angiokeratoma of clitoris: a rare lesion in an adolescent girl. Urology; 2008 Apr;71(4):604-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of clitoris: a rare lesion in an adolescent girl.
  • Angiokeratoma is a benign vascular lesion.
  • Angiokeratoma is more common in males, in whom it forms on the scrotal wall.
  • We present the case of a 14-year-old girl with a clitoral angiokeratoma.
  • To our knowledge, this is the first presented case of clitoral angiokeratoma in a child in English published reports.
  • [MeSH-major] Angiokeratoma / pathology. Clitoris. Skin Neoplasms / pathology

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  • (PMID = 18291515.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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25. del Pozo J, Fonseca E: Angiokeratoma circumscriptum naeviforme: successful treatment with carbon-dioxide laser vaporization. Dermatol Surg; 2005 Feb;31(2):232-6
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  • [Title] Angiokeratoma circumscriptum naeviforme: successful treatment with carbon-dioxide laser vaporization.
  • BACKGROUND: Angiokeratoma circumscriptum naeviforme (ACN) is an unusual type of localized angiokeratoma that occurs more frequently in females and is usually located on the buttocks or thighs, showing a unilateral distribution.
  • [MeSH-major] Angiokeratoma / diagnosis. Angiokeratoma / surgery. Skin Neoplasms / diagnosis. Skin Neoplasms / surgery

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  • (PMID = 15762221.001).
  • [ISSN] 1076-0512
  • [Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
  • [ISO-abbreviation] Dermatol Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 142M471B3J / Carbon Dioxide
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26. Kontogianni-Katsaros K, Kairi-Vassilatoy E, Grapsa D, Papadias K, Hasiakos D, Kondi-Pafitis A: Angiokeratoma of the vulva: a rare benign vascular tumor mimicking malignancy--case reports. Eur J Gynaecol Oncol; 2006;27(6):632-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of the vulva: a rare benign vascular tumor mimicking malignancy--case reports.
  • Four cases of angiokeratoma of the vulva diagnosed at our institution in a ten-year-period are reported and issues of the differential diagnosis are discussed.
  • [MeSH-major] Angiokeratoma / pathology. Skin Neoplasms / pathology. Vulvar Diseases / pathology

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  • (PMID = 17290602.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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27. Baruah J, Roy KK, Rahman SM, Kumar S, Pushparaj M, Mirdha AR: Angiokeratoma of vulva with coexisting human papilloma virus infection: a case report. Arch Gynecol Obstet; 2008 Aug;278(2):165-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma of vulva with coexisting human papilloma virus infection: a case report.
  • A wide local excision was performed and histopathological report confirmed a case of angiokeratoma.
  • To the best of our knowledge this is the first case of angiokeratoma of vulva following chronic HPV infection.
  • [MeSH-major] Angiokeratoma / virology. Human papillomavirus 6 / isolation & purification. Papillomavirus Infections / complications. Skin Neoplasms / virology. Vulva

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  • (PMID = 18193251.001).
  • [ISSN] 0932-0067
  • [Journal-full-title] Archives of gynecology and obstetrics
  • [ISO-abbreviation] Arch. Gynecol. Obstet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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28. Kanitakis J, Allombert C, Doebelin B, Deroo-Berger MC, Grande S, Blanc S, Claudy A: Fucosidosis with angiokeratoma. Immunohistochemical & electronmicroscopic study of a new case and literature review. J Cutan Pathol; 2005 Aug;32(7):506-11
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  • [Title] Fucosidosis with angiokeratoma. Immunohistochemical & electronmicroscopic study of a new case and literature review.
  • It presents clinically with neurological, skeletal, and cutaneous findings, including mainly angiokeratoma corporis diffusum.
  • Electronmicroscopic examination reveals characteristic electron-lucent cytoplasmic vacuolization present in several cell types of the skin and other tissues.
  • We present here a new patient suffering from fucosidosis with angiokeratoma, whose normal and diseased skin was studied by lightmicroscopy and electronmicroscopy.
  • [MeSH-major] Fabry Disease / pathology. Fucosidosis / pathology. Skin / pathology

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  • (PMID = 16008696.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Biomarkers; EC 3.2.1.51 / alpha-L-Fucosidase
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29. Molho-Pessach V, Bargal R, Abramowitz Y, Doviner V, Ingber A, Raas-Rothschild A, Ne'eman Z, Zeigler M, Zlotogorski A: Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new case and a novel mutation. J Am Acad Dermatol; 2007 Sep;57(3):407-12
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new case and a novel mutation.
  • BACKGROUND: Human beta-mannosidosis, a rare disorder of oligosaccharide catabolism, results from a deficiency of beta-mannosidase activity.
  • RESULTS: Histopathology of a skin biopsy specimen from the patient showed the characteristic findings of angiokeratoma.
  • The importance of angiokeratoma corporis diffusum as the clue to the diagnosis of beta-mannosidosis and other lysosomal storage diseases is emphasized.
  • [MeSH-minor] Adenine. Adult. Base Sequence. Codon, Terminator. Cytoplasm / ultrastructure. Exons. Female. Guanine. Humans. Microscopy, Electron. Molecular Sequence Data. Skin / pathology. Vacuoles / ultrastructure


30. Chedraoui A, Malek J, Tamraz H, Zaynoun S, Kibbi AG, Ghosn S: Acral pseudolymphomatous angiokeratoma of children in an elderly man: report of a case and review of the literature. Int J Dermatol; 2010 Feb;49(2):184-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Acral pseudolymphomatous angiokeratoma of children in an elderly man: report of a case and review of the literature.
  • Acral pseudolymphomatous angiokeratoma of children (APACHE) is clinically characterized by angiomatous papules that preferentially affect acral areas of children.
  • It is currently believed to be a variant of pseudolymphoma rather than angiokeratoma.
  • [MeSH-major] Angiokeratoma / pathology. Pseudolymphoma / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Aged. Biopsy, Needle. Child. Follow-Up Studies. Humans. Immunohistochemistry. Male. Physical Examination. Skin Diseases / diagnosis. Skin Diseases / pathology

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  • (PMID = 20465644.001).
  • [ISSN] 1365-4632
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 17
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31. Orteu CH, Jansen T, Lidove O, Jaussaud R, Hughes DA, Pintos-Morell G, Ramaswami U, Parini R, Sunder-Plassman G, Beck M, Mehta AB, FOS Investigators: Fabry disease and the skin: data from FOS, the Fabry outcome survey. Br J Dermatol; 2007 Aug;157(2):331-7
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  • [Title] Fabry disease and the skin: data from FOS, the Fabry outcome survey.
  • BACKGROUND: Fabry disease (also known as Anderson-Fabry disease) is a rare, X-linked lysosomal storage disorder that is characterized by accumulation of globotriaosylceramide throughout a range of tissues in the body.
  • OBJECTIVES: To ascertain the prevalence and nature of cutaneous manifestations in patients with Fabry disease and to relate these to the severity of systemic manifestations of the disease.
  • RESULTS: We confirm that the commonest disease manifestation is angiokeratoma.
  • Overall, 78% of males and 50% of females had one or more dermatological abnormality, the commonest being angiokeratoma (66% males, 36% females), hypohidrosis (53% males, 28% females), telangiectasia (23% males, 9% females) and lymphoedema (16% males, 6% females).
  • We demonstrate for the first time that the presence of cutaneous vascular lesions correlates with the severity of the systemic manifestations of the disease (pain, renal failure, cardiac disease, premature cerebrovascular disease) as assessed by a severity scoring system.
  • CONCLUSIONS: The FOS database is a useful epidemiological tool in establishing the variety and relevance of cutaneous manifestations in Fabry disease.
  • [MeSH-major] Fabry Disease / complications. Skin Diseases / etiology
  • [MeSH-minor] Adolescent. Adult. Age Factors. Angiokeratoma / epidemiology. Angiokeratoma / etiology. Angiokeratoma / pathology. Child. Europe / epidemiology. Female. Humans. Hypohidrosis / epidemiology. Hypohidrosis / etiology. Lymphedema / epidemiology. Lymphedema / etiology. Male. Middle Aged. Prevalence. Severity of Illness Index. Sex Factors. Skin Neoplasms / epidemiology. Skin Neoplasms / etiology. Skin Neoplasms / pathology. Telangiectasis / epidemiology. Telangiectasis / etiology. Telangiectasis / pathology


32. Navarro C, Teijeira S, Dominguez C, Fernandez JM, Rivas E, Fachal C, Barrera S, Rodriguez C, Iranzo P: Fabry disease: an ultrastructural comparative study of skin in hemizygous and heterozygous patients. Acta Neuropathol; 2006 Feb;111(2):178-85
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fabry disease: an ultrastructural comparative study of skin in hemizygous and heterozygous patients.
  • Fabry disease is a rare X-linked lysosomal storage disorder due to alpha galactosidase A deficiency, better known after the advent of a promising treatment, a periodical enzyme replacement.
  • Lysosomal deposits of ceramide trihexoside have been repeatedly documented in a wide range of tissues, including those found in angiokeratoma, the characteristic cutaneous lesion which allowed the definition of Fabry disease.
  • For that purpose, with electron microscopy and quantitative methods, we studied the extent of lysosomal deposits in dermal fibroblasts of normal-appearing skin in six females and nine men, enzymatically and genetically proven as to have Fabry disease, and results were compared.
  • We suggest that periodical ultrastructural examination of normal-appearing skin could be an indicator of the efficacy of enzyme replacement therapy and could help to evaluate results.
  • [MeSH-major] Fabry Disease / genetics. Fabry Disease / pathology. Heterozygote. Skin / ultrastructure

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  • (PMID = 16463201.001).
  • [ISSN] 0001-6322
  • [Journal-full-title] Acta neuropathologica
  • [ISO-abbreviation] Acta Neuropathol.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Glycosphingolipids; EC 3.2.1.22 / alpha-Galactosidase
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33. Feramisco JD, Fournier JB, Zedek DC, Venna SS: Eruptive angiokeratomas on the glans penis. Dermatol Online J; 2009;15(10):14
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Mibelli: hyperkeratotic papules on fingers or toes, solitary, multiple, or circumscriptum (grouped papules usually on an extremity); 4. angiokeratoma corporis diffusum, widespread papules that are a manifestation of one of several inherited lysozomal storage diseases.
  • [MeSH-major] Angiokeratoma / pathology. Penile Neoplasms / pathology. Skin Neoplasms / pathology

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  • [ErratumIn] Dermatol Online J. 2010 Sep;16(9):17. Zedek, Daniel C [added]
  • (PMID = 19951632.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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34. Mayer V, Maetzke J, Scharffetter-Kochanek K: [Punctate maculae on the back of the hands of a 44-year-old woman]. Hautarzt; 2009 May;60(5):428-32
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  • Our differential diagnosis includes idiopathic teleangiectases, teleangiectasia eruptiva perstans, angioma serpiginosum and angiokeratoma corporis diffusum Fabry.
  • [MeSH-major] Angiokeratoma / complications. Angiokeratoma / diagnosis. Hand / pathology. Keratosis / diagnosis. Keratosis / etiology. Macula Lutea / pathology. Skin Neoplasms / complications. Skin Neoplasms / diagnosis

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  • [Cites] Br J Dermatol. 1975 Dec;93(6):701-6 [1220816.001]
  • [Cites] J Dtsch Dermatol Ges. 2006 Aug;4(8):650-3 [16895567.001]
  • [Cites] Arch Dermatol. 1965 Dec;92(6):613-20 [5846315.001]
  • [Cites] Hautarzt. 1995 Dec;46(12):847-9 [8567268.001]
  • (PMID = 19225742.001).
  • [ISSN] 1432-1173
  • [Journal-full-title] Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete
  • [ISO-abbreviation] Hautarzt
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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35. Tennant LB, Mulliken JB, Perez-Atayde AR, Kozakewich HP: Verrucous hemangioma revisited. Pediatr Dermatol; 2006 May-Jun;23(3):208-15
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We analyzed the clinical and histopathologic characteristics of verrucous hemangioma, compared these findings to hyperkeratotic mimickers such as capillary-lymphatic malformation or capillary-venous malformation and angiokeratoma circumscriptum, and reconsidered whether the term verrucous hemangioma is appropriate in the current nosology of vascular anomalies.
  • Fourteen similar-appearing localized hyperkeratotic vascular lesions were identified by one surgeon as either angiokeratoma, angiokeratoma circumscriptum, capillary-venous malformation, capillary-lymphatic malformation, or verrucous hemangioma.
  • After histologic review, three lesions were designated as combined vascular malformations composed of capillaries, lymphatics, and veins, and none was designated as angiokeratoma.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology
  • [MeSH-minor] Adolescent. Angiokeratoma / pathology. Child. Child, Preschool. Diagnosis, Differential. Glucose Transporter Type 1 / metabolism. Humans. Infant. Infant, Newborn. Keratosis / pathology. Port-Wine Stain / pathology. Retrospective Studies


36. Buljan M, Poduje S, Situm M, Bulat V, Bolanča Z, Tomas D: Multiple angiokeratomas of the vulva: case report and literature review. Acta Dermatovenerol Croat; 2010;18(4):271-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Histopathologic analysis of the lesion confirmed the diagnosis of angiokeratoma, and all lesions were electrocauterized under local anesthesia.
  • [MeSH-major] Angiokeratoma / diagnosis. Skin Neoplasms / diagnosis. Vulvar Neoplasms / diagnosis

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  • (PMID = 21251446.001).
  • [ISSN] 1847-6538
  • [Journal-full-title] Acta dermatovenerologica Croatica : ADC
  • [ISO-abbreviation] Acta Dermatovenerol Croat
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Croatia
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37. Berk DR, Lind AC, Bayliss SJ: Acral angiokeratomas in a patient with Turner syndrome. Pediatr Dermatol; 2010 Nov-Dec;27(6):662-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Several types of vascular anomalies have been described in patients with Turner syndrome, including cutaneous lymphatic malformations, vascular anomalies of the heart and aorta, acral venous malformations, and intestinal vascular anomalies.
  • Biopsy showed acral skin with focal epidermal acanthosis that was centered on a dilated superficial vessel, consistent with an angiokeratoma.
  • Lysosomal enzyme assays were normal, and she did not demonstrate any other features of a lysosomal storage disorder.
  • [MeSH-major] Angiokeratoma / complications. Angiokeratoma / pathology. Skin Neoplasms / complications. Skin Neoplasms / pathology. Turner Syndrome / complications

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  • [Copyright] © 2010 Wiley Periodicals, Inc.
  • (PMID = 21510021.001).
  • [ISSN] 1525-1470
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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38. Rákóczi E, Görögh S, Grubits J, Erdos M, Garzuly F, Hahn K, Bencsik K, Vécsei L, Trinn C, Kristóf E, Mogyorósy G, Tóth B, Maródi L: [Molecular pathology and clinical manifestations of Fabry disease]. Orv Hetil; 2007 Jun 10;148(23):1087-94
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Fabry disease is a rare, progressive lysosomal storage disorder caused by mutation in the GAL gene and an impaired function of the alpha-galactosidase A enzyme.
  • The enzymatic defect results in the progressive accumulation of glycosphingolipids in endothelial cells, smooth muscle cells, leucocytes and fibroblasts leading to organ damage in the skin, eye, nervous system, kidney and heart.
  • Major clinical manifestations include acroparesthesis, angiokeratoma, corneal opacities, vascular diseases of the heart, kidney, and the central nervous system.
  • The most common disease-specific manifestation was angiokeratoma in males, and eye symptoms in females.
  • [MeSH-minor] Adolescent. Adult. Aged. Angiokeratoma / etiology. Brain Ischemia / etiology. Child. Child, Preschool. Female. Genetic Predisposition to Disease. Heterozygote. Homozygote. Humans. Kidney / pathology. Male. Middle Aged. Proteinuria / etiology

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  • (PMID = 17545117.001).
  • [ISSN] 0030-6002
  • [Journal-full-title] Orvosi hetilap
  • [ISO-abbreviation] Orv Hetil
  • [Language] hun
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Hungary
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39. Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Bouguila J, Sanhaji H, Miladi N, Maire I, Caillaud C, Kaabachi N, Ben Dridi MF: Phenotypic spectrum of fucosidosis in Tunisia. J Inherit Metab Dis; 2008 Dec;31 Suppl 2:S313-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Fucosidosis (OMIM 230000) is a rare autosomal recessive lysosomal disorder due to deficient α-L-fucosidase activity(EC 3.2.1.51), leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues.
  • This distinction was determined by the presence or absence of angiokeratoma and age of death.
  • Clinical features consist of variable mental retardation (all patients), progressive spastic quadriplegia (6/10 cases), coarse facies (9/10 cases), growth retardation (7/9 cases), visceromegaly (3 cases), angiokeratoma corporis diffusum (4 cases), recurrent bronchopneumonias (all cases), seizures (4 cases) and variable degrees of dysostosis multiplex (all cases).
  • [MeSH-minor] Angiokeratoma / epidemiology. Cause of Death. Child Development. Child, Preschool. Developmental Disabilities / epidemiology. Female. Health Surveys. Humans. Infant. Male. Nervous System Diseases / epidemiology. Phenotype. Prognosis. Severity of Illness Index. Skin Neoplasms / epidemiology. Time Factors. Tunisia / epidemiology

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  • (PMID = 18651239.001).
  • [ISSN] 1573-2665
  • [Journal-full-title] Journal of inherited metabolic disease
  • [ISO-abbreviation] J. Inherit. Metab. Dis.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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40. Aidagulova SV, Zhornik TM, Nepomnyashchikh DL, Marinkin IO, Vinogradova EV, Nokhrina ZhV: Ultrastructural modification of the endothelium in placental insufficiency and microangiopathies. Bull Exp Biol Med; 2009 May;147(5):650-4

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  • Structural reorganization of endotheliocytes was studied on models of various pathological processes: placental dysfunction, glomerular pathology, vibration syndrome, antiphospholipid syndrome, and diffuse angiokeratoma, all of these characterized by endothelial insufficiency.
  • [MeSH-minor] Adolescent. Adult. Antiphospholipid Syndrome / pathology. Fabry Disease / pathology. Female. Humans. Kidney Glomerulus / pathology. Kidney Glomerulus / ultrastructure. Male. Microscopy, Electron, Transmission. Middle Aged. Pregnancy. Skin / pathology. Skin / ultrastructure. Stomach / pathology. Stomach / ultrastructure. Young Adult

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  • (PMID = 19907761.001).
  • [ISSN] 1573-8221
  • [Journal-full-title] Bulletin of experimental biology and medicine
  • [ISO-abbreviation] Bull. Exp. Biol. Med.
  • [Language] eng; rus
  • [Publication-type] Journal Article
  • [Publication-country] United States
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41. Mirceva V, Hein R, Ring J, Möhrenschlager M: A case of multiple angiomas without any angiokeratomas in a female heterozygote with Fabry disease. Australas J Dermatol; 2010 Feb;51(1):36-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Fabry Disease / diagnosis. Hemangioma / diagnosis. Heterozygote Detection. Skin Neoplasms / diagnosis. alpha-Galactosidase / genetics
  • [MeSH-minor] Angiokeratoma / diagnosis. Angiokeratoma / genetics. Angiokeratoma / pathology. Female. Heterozygote. Humans. Leukocytes / enzymology. Male. Middle Aged

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  • (PMID = 20148840.001).
  • [ISSN] 1440-0960
  • [Journal-full-title] The Australasian journal of dermatology
  • [ISO-abbreviation] Australas. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] EC 3.2.1.22 / alpha-Galactosidase
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42. Jansen T, Brokalaki E, Hillen U, Hentschke M, Grabbe S: [Manifestation of Fabry disease in a heterozygous female patient. New perspectives using enzyme replacement therapy]. Dtsch Med Wochenschr; 2006 Jul 14;131(28-29):1590-3
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  • She was admitted to our hospital because of skin lesions that had developed over the last 8 years.
  • Histological examination revealed lipid deposits within the endothelial cells of the skin.
  • [MeSH-minor] Abdomen. Adult. Angiokeratoma / etiology. Buttocks. Corneal Opacity / etiology. Female. Heterozygote. Hip. Humans. Isoenzymes / administration & dosage. Isoenzymes / therapeutic use. Mitral Valve Prolapse / etiology. Point Mutation. Skin Neoplasms / etiology

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  • (PMID = 16823707.001).
  • [ISSN] 0012-0472
  • [Journal-full-title] Deutsche medizinische Wochenschrift (1946)
  • [ISO-abbreviation] Dtsch. Med. Wochenschr.
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Isoenzymes; EC 3.2.1.- / agalsidase alfa; EC 3.2.1.22 / alpha-Galactosidase
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43. Zaballos P, Daufí C, Puig S, Argenziano G, Moreno-Ramírez D, Cabo H, Marghoob AA, Llambrich A, Zalaudek I, Malvehy J: Dermoscopy of solitary angiokeratomas: a morphological study. Arch Dermatol; 2007 Mar;143(3):318-25
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  • Conclusion Dermoscopy is helpful in improving the diagnostic accuracy of solitary angiokeratomas and allows the observer to differentiate them from other cutaneous tumors such as malignant melanomas and pigmented basal cell carcinomas.
  • [MeSH-major] Angiokeratoma / pathology. Dermoscopy. Skin Neoplasms / pathology

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  • (PMID = 17372096.001).
  • [ISSN] 0003-987X
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
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44. Choudhury S, Meehan S, Shin HT: Fabry disease: an atypical presentation. Pediatr Dermatol; 2005 Jul-Aug;22(4):334-7
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  • [MeSH-major] Angiokeratoma / etiology. Fabry Disease / diagnosis. Skin Neoplasms / etiology


45. Happle R: What is a capillary malformation? J Am Acad Dermatol; 2008 Dec;59(6):1077-9

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  • There are at least nine different skin disorders fulfilling the criteria of a capillary malformation.
  • Examples include nevus anemicus, cutis marmorata telangiectatica congenita, angiokeratoma circumscriptum, and several vascular lesions that, in the author's view, do not represent nevi, such as the nuchal or glabellar salmon patch and the cutaneous changes of Rendu-Osler disease.
  • Hence, I propose that we should use "capillary malformation" as an umbrella term and not as a name for a specific cutaneous entity.
  • [MeSH-minor] Humans. Nevus / classification. Skin / blood supply. Skin Neoplasms / classification. Telangiectasis / classification

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  • (PMID = 19022106.001).
  • [ISSN] 1097-6787
  • [Journal-full-title] Journal of the American Academy of Dermatology
  • [ISO-abbreviation] J. Am. Acad. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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46. Morais P, Santos AL, Baudrier T, Mota AV, Oliveira JP, Azevedo F: Angiokeratomas of Fabry successfully treated with intense pulsed light. J Cosmet Laser Ther; 2008 Dec;10(4):218-22
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  • Fabry disease (FD) is a rare X-linked lysosomal storage disorder resulting from the deficient activity of the enzyme alpha-galactosidase A.
  • The IPL source can be considered a suitable, effective and safe treatment modality for these cutaneous lesions that typically affect patients with FD, with no need for local anesthesia and with very satisfactory cosmetic results.
  • [MeSH-major] Angiokeratoma / therapy. Fabry Disease / pathology. Phototherapy / methods. Skin Neoplasms / therapy

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  • (PMID = 18830871.001).
  • [ISSN] 1476-4180
  • [Journal-full-title] Journal of cosmetic and laser therapy : official publication of the European Society for Laser Dermatology
  • [ISO-abbreviation] J Cosmet Laser Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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47. AADELFA (Asociación Argentina de estudio de enfermedad de Fabry y otras enfermedades lisosomales): [Evaluation of patients with Fabry disease in Argentina]. Medicina (B Aires); 2010;70(1):37-43
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  • Fabry disease is an X- linked lysosomal disorder due to deficient activity of the enzyme alpha galactosidase A which leads to multisystemic storage of globotriaosylceramide with neurologic, gastrointestinal, cardiac, renal, skin and ophtalmological involvement.
  • Recent studies indicate that heterozygous females develop symptoms similar to the males, but comparative information regarding the relative frequency of clinical manifestations, age of onset and severity of the disorder between males and females with Fabry disease is not available in Argentina.
  • Fabry disease is an underdiagnosed and potentially fatal disorder that affects both sexes.
  • The availability of enzyme replacement therapy should stimulate the identification of signs and symptoms suggestive of this disorder, to allow earlier diagnosis and treatment.
  • [MeSH-minor] Adult. Aged. Angiokeratoma / diagnosis. Angiokeratoma / etiology. Argentina. Corneal Opacity / diagnosis. Corneal Opacity / etiology. Female. Heterozygote. Humans. Hypertrophy, Left Ventricular / diagnosis. Hypertrophy, Left Ventricular / etiology. Male. Middle Aged. Mutation. Severity of Illness Index. Sex Factors. Young Adult

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  • (PMID = 20228022.001).
  • [ISSN] 0025-7680
  • [Journal-full-title] Medicina
  • [ISO-abbreviation] Medicina (B Aires)
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Argentina
  • [Chemical-registry-number] EC 3.2.1.22 / alpha-Galactosidase
  • [Investigator] Doxastakis G; Ferrari G; Ana María E; Kisinovsky I; Cáceres G; Bianchi S; Aguilar R; Aggio M; Tarabuso A; Peralta I; Reisin R; Nápoli G; Pardal A; Marchesoni C; Neumann P; Ebner R; Martínez P; Penna J; Rozenfeld P
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48. Dobrovolskiene R, Utkus A, Tumiene B, Rainiene T, Czartoryska B: [Fabry's disease: a clinical case and literature review]. Medicina (Kaunas); 2007;43 Suppl 1:139-44
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  • Fabry's disease is a congenital disorder of glycosphingolipid metabolism with an X-linked recessive inheritance, presenting with typical symptoms of pain crises, acroparesthesias, cutaneous and mucosal angiokeratomas, hypohidrosis, heart and kidney lesions, and other symptoms, which are described below.
  • [MeSH-minor] Angiokeratoma / diagnosis. Clinical Enzyme Tests. Humans. Lysosomes / enzymology. Phenotype. Skin Neoplasms / diagnosis. Thorax. Time Factors

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  • (PMID = 17551292.001).
  • [ISSN] 1648-9144
  • [Journal-full-title] Medicina (Kaunas, Lithuania)
  • [ISO-abbreviation] Medicina (Kaunas)
  • [Language] lit
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Lithuania
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49. Astner S, González S, Cuevas J, Röwert-Huber J, Sterry W, Stockfleth E, Ulrich M: Preliminary evaluation of benign vascular lesions using in vivo reflectance confocal microscopy. Dermatol Surg; 2010 Jul;36(7):1099-110
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  • BACKGROUND: Reflectance confocal microscopy (RCM) is a novel noninvasive imaging technique for in vivo evaluation of cutaneous lesions at near-histologic resolution.
  • The applicability of RCM for various neoplastic and inflammatory skin diseases has been shown, but a descriptive evaluation of different vascular lesions has not yet been performed.
  • MATERIALS AND METHODS: Seven patients with a clinical diagnosis of vascular lesion, including spider angioma, venous lake, cherry angioma, pyogenic granuloma, port wine stain, angiokeratoma, and lymphangioma, participated in this study.
  • Skin sites were systematically analyzed using RCM, and biopsy was obtained for clinically indeterminate lesions.
  • [MeSH-major] Granuloma, Pyogenic / pathology. Lymphangioma / pathology. Microscopy, Confocal / methods. Neoplasms, Vascular Tissue / pathology. Port-Wine Stain / pathology. Skin Neoplasms / pathology

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  • (PMID = 20653723.001).
  • [ISSN] 1524-4725
  • [Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
  • [ISO-abbreviation] Dermatol Surg
  • [Language] eng
  • [Publication-type] Controlled Clinical Trial; Journal Article
  • [Publication-country] United States
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50. Lee MW, Lee DK, Choi JH, Moon KC, Koh JK: Clinicopathologic study of cutaneous pseudolymphomas. J Dermatol; 2005 Jul;32(7):594-601
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  • [Title] Clinicopathologic study of cutaneous pseudolymphomas.
  • A study was conducted to determine the clinical and histopathologic findings of cutaneous pseudolymphomas.
  • The histologic patterns were diverse, MF-like, perivascular/periadnexal, nodular, diffuse, pseudolymphomatous folliculitis, and acral pseudolymphomatous angiokeratoma of children (APACHE) patterns.
  • The differentiation between cutaneous lymphomas and pseudolymphomas must depend on a constellation of criteria, never on a single criterion.
  • [MeSH-major] Pseudolymphoma / pathology. Skin Diseases / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Child. Child, Preschool. Female. Humans. Male. Middle Aged. Skin / pathology

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  • (PMID = 16335878.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Japan
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51. Garrido-Ríos AA, Sánchez-Velicia L, Marino-Harrison JM, Torrero-Antón MV, Miranda-Romero A: [A histopathologic and imaging study of verrucous hemangioma]. Actas Dermosifiliogr; 2008 Nov;99(9):723-6
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  • The terms verrucous hemangioma and angiokeratoma circumscriptum have been used interchangeably in the literature to define clinically similar lesions.
  • From a histologic perspective, however, angiokeratoma circumscriptum is limited to the papillary dermis whereas verrucous hemangioma extends as far as the hypodermis.
  • We describe the case of a 38-year-old woman who consulted for a lesion on the right thigh that was initially diagnosed as angiokeratoma; magnetic resonance imaging, however, led to a final diagnosis of verrucous hemangioma.
  • [MeSH-minor] Adult. Female. Humans. Skin Neoplasms / diagnosis. Skin Neoplasms / pathology

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  • [CommentIn] Actas Dermosifiliogr. 2009 Jun;100(5):437; author reply 438-9 [19558927.001]
  • (PMID = 19087812.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
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52. Koc M, Kavala M, Kocatürk E, Zemheri E, Zindanci I, Sudogan S, Kural E: An unusual vascular tumor: verrucous hemangioma. Dermatol Online J; 2009;15(11):7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiokeratoma / pathology. Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 19951643.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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53. Kuzman T, Juri J, Mrsić M, Jeren-Strujić B, Mandić Z, Sikić J: [Ocular findings in Fabry's disease]. Acta Med Croatica; 2006;60(2):163-6
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  • INTRODUCTION: Fabry's disease is a recessive X-linked disorder that results from a deficiency of the lysosomal hydrolase a-galactosidase A (alpha-Gal A).
  • Subsequently, angiokeratoma and ocular signs develop until, in most cases after the third decade of life, severe renal dysfunction or cardiomyopathy becomes obvious.
  • During further evaluation nephrologist suspected Fabry's disease, because patient had skin changes early referred as petechiae, and acroparesthesias.
  • Physical status: angiokeratoma on gluteat regions and upper arms.

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  • (PMID = 16848212.001).
  • [ISSN] 1330-0164
  • [Journal-full-title] Acta medica Croatica : c̆asopis Hravatske akademije medicinskih znanosti
  • [ISO-abbreviation] Acta Med Croatica
  • [Language] hrv
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Croatia
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54. Cybulla M, Walter K, Neumann HP, Widmer U, Schärer M, Sunder-Plassmann G, Jansen T, Rolfs A, Beck M: [Fabry disease: demographic data since introduction of enzyme replacement therapy]. Dtsch Med Wochenschr; 2007 Jul 5;132(28-29):1505-9
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  • BACKGROUND AND OBJECTIVE: Fabry's disease is a rare, X-chromosome linked recessive lysosomal storage disorder.
  • In its course multiple organ damage occurs, e.g. in skin, nerves, kidneys and heart.
  • RESULTS: Typical symptoms - acroparesthesias, joint pain, hypohidrosis, fever and angiokeratoma - have their onset in childhood (mean age nine years).

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  • (PMID = 17607649.001).
  • [ISSN] 1439-4413
  • [Journal-full-title] Deutsche medizinische Wochenschrift (1946)
  • [ISO-abbreviation] Dtsch. Med. Wochenschr.
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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55. Germain DP: Fabry disease. Orphanet J Rare Dis; 2010;5:30
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  • Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal α-galactosidase A activity.
  • Classically affected hemizygous males, with no residual α-galactosidase A activity may display all the characteristic neurological (pain), cutaneous (angiokeratoma), renal (proteinuria, kidney failure), cardiovascular (cardiomyopathy, arrhythmia), cochleo-vestibular and cerebrovascular (transient ischemic attacks, strokes) signs of the disease while heterozygous females have symptoms ranging from very mild to severe.

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  • (PMID = 21092187.001).
  • [ISSN] 1750-1172
  • [Journal-full-title] Orphanet journal of rare diseases
  • [ISO-abbreviation] Orphanet J Rare Dis
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] EC 3.2.1.22 / alpha-Galactosidase
  • [Other-IDs] NLM/ PMC3009617
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56. Zlotoff BJ, Bang RH, Padilla RS, Morrison L: Cutaneous angiokeratoma and venous malformations in a Hispanic-American patient with cerebral cavernous malformations. Br J Dermatol; 2007 Jul;157(1):210-2
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cutaneous angiokeratoma and venous malformations in a Hispanic-American patient with cerebral cavernous malformations.
  • [MeSH-major] Angiokeratoma / genetics. Intracranial Arteriovenous Malformations / genetics. Microtubule-Associated Proteins / genetics. Proto-Oncogene Proteins / genetics. Skin Neoplasms / genetics

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  • (PMID = 17578448.001).
  • [ISSN] 0007-0963
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
  • [Chemical-registry-number] 0 / KRIT1 protein, human; 0 / Microtubule-Associated Proteins; 0 / Proto-Oncogene Proteins
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57. Nomelini RS, Pansani PL, Guimarães PD, Martins-Filho A, Barcelos AC, Murta EF: Vulvar angiokeratoma. J Obstet Gynaecol; 2010 May;30(4):418-9
MedlinePlus Health Information. consumer health - Vulvar Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Vulvar angiokeratoma.
  • [MeSH-major] Angiokeratoma / pathology. Skin Neoplasms / pathology. Vulva / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 20455737.001).
  • [ISSN] 1364-6893
  • [Journal-full-title] Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
  • [ISO-abbreviation] J Obstet Gynaecol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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58. Cakmak SK, Gönül M, Gül U, Gündüz H, Demiriz M, Ustüner E: Unilateral angiokeratoma of the breast. Eur J Dermatol; 2009 Jan-Feb;19(1):75-6
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unilateral angiokeratoma of the breast.
  • [MeSH-major] Angiokeratoma / diagnosis. Breast. Skin Neoplasms / diagnosis

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  • (PMID = 19171535.001).
  • [ISSN] 1167-1122
  • [Journal-full-title] European journal of dermatology : EJD
  • [ISO-abbreviation] Eur J Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] France
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59. Saha M, Barlow R, Bunker CB: Angiokeratoma circumscriptum of the penis. Br J Dermatol; 2006 Apr;154(4):775-6
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma circumscriptum of the penis.
  • [MeSH-major] Angiokeratoma / pathology. Penile Neoplasms / pathology. Skin Neoplasms / pathology

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  • (PMID = 16536830.001).
  • [ISSN] 0007-0963
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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60. Mittal R, Aggarwal A, Srivastava G: Angiokeratoma circumscriptum: a case report and review of the literature. Int J Dermatol; 2005 Dec;44(12):1031-4
The Weizmann Institute of Science GeneCards and MalaCards databases. gene/protein/disease-specific - MalaCards for angiokeratoma circumscriptum .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma circumscriptum: a case report and review of the literature.
  • [MeSH-major] Angiokeratoma / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 16409270.001).
  • [ISSN] 0011-9059
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 31
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61. Sahin MT, Türel-Ermertcan A, Oztürkcan S, Türkdogan P: Thrombosed solitary angiokeratoma of Mibelli simulating malignant melanoma: the importance of dermoscopy in differential diagnosis. J Eur Acad Dermatol Venereol; 2006 Jan;20(1):102-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Thrombosed solitary angiokeratoma of Mibelli simulating malignant melanoma: the importance of dermoscopy in differential diagnosis.
  • [MeSH-major] Angiokeratoma / diagnosis. Dermoscopy. Thrombosis / diagnosis
  • [MeSH-minor] Adolescent. Diagnosis, Differential. Humans. Male. Melanoma / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 16405622.001).
  • [ISSN] 0926-9959
  • [Journal-full-title] Journal of the European Academy of Dermatology and Venereology : JEADV
  • [ISO-abbreviation] J Eur Acad Dermatol Venereol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
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62. Ghorpade A: Naevoid blaschkoid red-blue lesions in an Indian boy. Angiokeratoma corporis naeviforme along the lines of Blaschko. Clin Exp Dermatol; 2010 Apr;35(3):e79-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Naevoid blaschkoid red-blue lesions in an Indian boy. Angiokeratoma corporis naeviforme along the lines of Blaschko.
  • [MeSH-major] Angiokeratoma / pathology. Leg. Nevus, Blue / pathology. Skin Neoplasms / pathology

  • MedlinePlus Health Information. consumer health - Skin Cancer.
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  • (PMID = 20500192.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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63. Fauchais AL, Prey S, Ouatara B, Vidal E, Sparsa A: Angiokeratoma regression in a Fabry disease after treatment with agalsidase-beta: clinical effectiveness marker? J Eur Acad Dermatol Venereol; 2010 Jun;24(6):737-8
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiokeratoma regression in a Fabry disease after treatment with agalsidase-beta: clinical effectiveness marker?
  • [MeSH-major] Angiokeratoma / drug therapy. Enzyme Replacement Therapy / methods. Fabry Disease / drug therapy. Isoenzymes / therapeutic use. Skin Neoplasms / drug therapy. alpha-Galactosidase / therapeutic use

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  • (PMID = 19925601.001).
  • [ISSN] 1468-3083
  • [Journal-full-title] Journal of the European Academy of Dermatology and Venereology : JEADV
  • [ISO-abbreviation] J Eur Acad Dermatol Venereol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Isoenzymes; EC 3.2.1.- / agalsidase beta; EC 3.2.1.22 / alpha-Galactosidase
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64. Bonnetblanc JM: [Physiological aspects of the genital area]. Ann Dermatol Venereol; 2005 Aug-Sep;132(8-9 Pt 1):721-2
MedlinePlus Health Information. consumer health - Skin Conditions.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Genital Diseases, Male / physiopathology. Skin Diseases / physiopathology
  • [MeSH-minor] Angiokeratoma / physiopathology. Humans. Male. Skin Neoplasms / physiopathology

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  • (PMID = 16230930.001).
  • [ISSN] 0151-9638
  • [Journal-full-title] Annales de dermatologie et de vénéréologie
  • [ISO-abbreviation] Ann Dermatol Venereol
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
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65. Karadag AS, Simsek GG: Multiple angiokeratomas on the breast. Indian J Dermatol Venereol Leprol; 2009 Jul-Aug;75(4):451-2
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiokeratoma / diagnosis. Breast / pathology. Skin Neoplasms / diagnosis

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  • (PMID = 19584485.001).
  • [ISSN] 0973-3922
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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66. Clark SM, Beachkofsky TM, Wisco OJ, Hodson DS: Verrucous papule on thigh. J Fam Pract; 2010 Nov;59(11):645-8
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiokeratoma / pathology. Skin Neoplasms / pathology. Thigh / pathology

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  • (PMID = 21060903.001).
  • [ISSN] 1533-7294
  • [Journal-full-title] The Journal of family practice
  • [ISO-abbreviation] J Fam Pract
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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67. Möhrenschlager M, Henkel V, Ring J: Angiokeratomas, Fabry disease and enzyme replacement therapy: still a challenge. Br J Dermatol; 2005 Jan;152(1):177-8; author reply 178-9
MedlinePlus Health Information. consumer health - Skin Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiokeratoma / diagnosis. Fabry Disease / drug therapy. Skin Neoplasms / diagnosis. alpha-Galactosidase / therapeutic use

  • Genetic Alliance. consumer health - BabyFirstTest - Fabry Disease.
  • Genetic Alliance. consumer health - Fabry Disease.
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  • [CommentOn] Br J Dermatol. 2004 Mar;150(3):575-7 [15030345.001]
  • (PMID = 15656825.001).
  • [ISSN] 0007-0963
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] England
  • [Chemical-registry-number] EC 3.2.1.22 / alpha-Galactosidase
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