Generalized Telangiectasia

Becker, S. William

doi:10.1001/archderm.1926.02370220018003

Cited by 38 publications

(2 citation statements)

References 21 publications

(1 reference statement)

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“…At variance with CCV, GET is more common in women and can rarely also involve the oral mucosa and conjunctiva. In contrast to CCV, in GET there are dilated vessel walls, which consist of thickened endothelial cells, but without any deposition of amorphous hyaline material [2,9]. …”

Section: Discussionmentioning

confidence: 99%

Cutaneous Collagenous Vasculopathy: A Rare Form of Microangiopathy Successfully Treated with a Combination of Multiplex Laser and Optimized Pulsed Light with a Review of the Literature

et al. 2015

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Cutaneous collagenous vasculopathy (CCV) is a rare idiopathic microangiopathy of the cutaneous vasculature characterized histologically by the presence of dilated small blood vessels with flat endothelial cells and thickened walls containing hyaline material in the upper dermis. We report an elderly patient presenting with an extensive form of CCV involving the trunk, upper and lower limbs. She was treated with Multiplex PDL 595-nm/Nd:YAG 1,064-nm laser and optimized pulsed light. This approach, which has never been reported for CCV so far, resulted in a striking and almost complete clearance of the widespread lesions. We here review our knowledge about CCV and therapeutic options available with a survey of the literature.

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Section: Discussionmentioning

confidence: 99%

Cutaneous Collagenous Vasculopathy: A Rare Form of Microangiopathy Successfully Treated with a Combination of Multiplex Laser and Optimized Pulsed Light with a Review of the Literature

et al. 2015

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“…Generalized essential telangiectasia is much more common among adult women without family history. It occurs most frequently on the lower extremities and tends to extend progressively (8)(9)(10)(11)(12).…”

Section: Discussionmentioning

confidence: 99%

Hereditary Benign Telangiectasia: Two Case Reports

Puppin

Rybojad

Morel

1992

The Journal of Dermatology

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We present two cases of hereditary benign telangiectasia (HBT) in which the genetic findings are compatible with an autosomal dominant hypothesis. The lesions persisted indefinitely for many years without effect on the general health of the patients. The term hereditary benign telangiectasia distinguishes the disorder from the more serious hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber). The etiology remains unknown. The condition causes only cosmetic disability and is not associated with any other diseases.

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Skin Diseases of Endocrine Origin (Dyshormonal Dermatoses)

Bloch¹

1929

Arch Derm Syphilol

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Generalized Telangiectasia

Cited by 38 publications

References 21 publications

Cutaneous Collagenous Vasculopathy: A Rare Form of Microangiopathy Successfully Treated with a Combination of Multiplex Laser and Optimized Pulsed Light with a Review of the Literature

Cutaneous Collagenous Vasculopathy: A Rare Form of Microangiopathy Successfully Treated with a Combination of Multiplex Laser and Optimized Pulsed Light with a Review of the Literature

Hereditary Benign Telangiectasia: Two Case Reports

Skin Diseases of Endocrine Origin (Dyshormonal Dermatoses)

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