Pyogenic granuloma within unilateral dermatomal superficial telangiectasia

Mazereeuw‐Hautier, J.; Thibaut, I; Jl, Bonafé

doi:10.1046/j.1365-2133.2003.05195.x

Cited by 14 publications

(4 citation statements)

References 7 publications

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“…Until today, unilateral naevoid telangiectasia of the patchy type is a poorly defined disorder . It is included here for heuristic reasons.…”

Section: Capillary Malformations That Perhaps Represent Naevimentioning

confidence: 99%

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Capillary malformations: a classification using specific names for specific skin disorders

Happle

2015

Acad Dermatol Venereol

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The name capillary malformation has caused much confusion because it is presently used to designate numerous quite different disorders such as naevus flammeus, the salmon patch, the vascular naevus of the hereditary 'megalencephaly-capillary malformation syndrome' and the skin lesions of non-hereditary traits such as 'capillary malformation-arteriovenous malformation' and 'microcephaly-capillary malformation'. To avoid such bewilderment, the present review describes the distinguishing clinical and genetic criteria of 20 different capillary malformations, and a specific name is given to all of them. The group of capillary naevi includes naevus flammeus, port-wine naevus of the Proteus type, port-wine naevus of the CLOVES type, naevus roseus, rhodoid naevus, cutis marmorata telangiectatica congenita, congenital livedo reticularis, segmental angioma serpiginosum, naevus anaemicus, naevus vascularis mixtus and angiokeratoma circumscriptum. Capillary lesions that perhaps represent naevi are the mesotropic port-wine patch, Carter-Mirzaa macules, unilateral punctate telangiectasia and unilateral naevoid telangiectasia of the patchy type. Capillary malformations that do not represent naevi include X-linked angiokeratoma corporis diffusum (Fabry disease), autosomal dominant angiokeratoma corporis diffusum, hereditary haemorrhagic telangiectasia, hereditary angioma serpiginosusm and the salmon patch. In this way, we are able to discriminate between various non-hereditary capillary naevi such as naevus roseus and the hereditary rhodoid naevus and several hereditary traits that do not represent naevi such as angiokeratoma corporis diffusum and hereditary haemorrhagic telangiectasia; between four different types of port-wine stains, three of them being lateralized and one being mesotropic; between cutis marmorata telangiectatica congenita and congenital livedo reticularis; between telangiectatic naevi and the vasoconstrictive naevus anaemicus; and between two different types of angiokeratoma corporis diffusum. Finally, arguments are presented why the salmon patch ('stork bite', 'naevus simplex') cannot be categorized as a naevus.

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“…Until today, unilateral naevoid telangiectasia of the patchy type is a poorly defined disorder . It is included here for heuristic reasons.…”

Section: Capillary Malformations That Perhaps Represent Naevimentioning

confidence: 99%

“…107,112,113 Unilateral naevoid telangiectasia of the patchy type Until today, unilateral naevoid telangiectasia of the patchy type is a poorly defined disorder. [114][115][116] It is included here for heuristic reasons. The disorder is characterized by light red macules of various sizes.…”

Section: Figurementioning

confidence: 99%

Capillary malformations: a classification using specific names for specific skin disorders

Happle

2015

Acad Dermatol Venereol

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“…In 1983, Wilkin et al 2 proposed a system for classifying UNT ( Table 1). We have reviewed the literature and found reports of many new cases [11][12][13][14][15][16][17][18][19][20][21][22][23][24][25] that provide new information. The UNT patient should be evaluated for associated diseases, although some associations may be coincidental.…”

Section: Discussionmentioning

confidence: 99%

Unilateral nevoid telangiectasia: case report and proposal for new classification system

2013

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“…Cutaneous lesions are predominantly located on the third and fourth cervical dermatomes 4 . UNT has also been described in association with a few other cutaneous conditions, such as polymorphic light eruption 5 or pyogenic granuloma 6 …”

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confidence: 99%

Unilateral naevoid telangiectasia in a young man after chemotherapy: a simple coincidence or a new clinical association?

Rodríguez-Martín¹,

Sáez²,

Carnerero

et al. 2006

Acad Dermatol Venereol

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1001placebo or active comparators, but not one type of treatment vs. another or vs. a combination of both. In our case, complete symptom resolution followed combined use of both oral paroxetine and local triamcinolone. We would conclude that the two types of treatment are not incompatible in the same patient and may both be applied to obtain early resolution of AA and associated psychiatric comorbidity. It would be interesting to compare each treatment individually vs. each other and vs. their combination in different orders (e.g. antidepressant first, triamcinolone after or vice versa ) to establish whether there is a sequentially ordered pathophysiological link between psychological/psychiatric and somatic symptoms in AA with comorbid depression.

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Pyogenic granuloma within unilateral dermatomal superficial telangiectasia

Cited by 14 publications

References 7 publications

Capillary malformations: a classification using specific names for specific skin disorders

Capillary malformations: a classification using specific names for specific skin disorders

Unilateral nevoid telangiectasia: case report and proposal for new classification system

Unilateral naevoid telangiectasia in a young man after chemotherapy: a simple coincidence or a new clinical association?

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