2012
DOI: 10.1016/j.jaad.2012.01.036
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Connective tissue nevi in children: Institutional experience and review

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Cited by 38 publications
(42 citation statements)
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References 55 publications
(74 reference statements)
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“…There is no estimated incidence or prevalence of CTN. The lesions can be acquired or congenital, sporadic or inherited . They may be features of several syndromes, such as Buschke–Ollendorff syndrome , Proteus syndrome , tuberous sclerosis , or multiple endocrine neoplasia type 1 .…”
Section: Discussionmentioning
confidence: 99%
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“…There is no estimated incidence or prevalence of CTN. The lesions can be acquired or congenital, sporadic or inherited . They may be features of several syndromes, such as Buschke–Ollendorff syndrome , Proteus syndrome , tuberous sclerosis , or multiple endocrine neoplasia type 1 .…”
Section: Discussionmentioning
confidence: 99%
“…In 1980, Uitto et al first classified CTN. More recently, McCuaig et al proposed a new, modified classification, dividing CTN into acquired and inherited lesions and classifying them also according to the major component of the extracellular matrix: collagenoma if the major component is collagen, elastoma if it is elastin, and mucinous nevus in the case of proteoglycans.…”
Section: Discussionmentioning
confidence: 99%
“…These lesions are very firm and contain deep sulci that resemble the brain, for which the lesion is named. Histology sections of CCTN show massively expanded dermis filled with thick collagen bundles (Figure 1d-f) (McCuaig et al 2012). Epidermal nevi (EN) can be non-syndromic or occur as part of several syndromes including PS (Happle 2010).…”
mentioning
confidence: 99%
“…Connective tissue nevi are dermal hamartomas characterized by an abnormal accumulation of collagen, elastin, or proteoglycans . Uitto et al first classified connective tissue nevi in 1980.…”
Section: Discussionmentioning
confidence: 99%