1996
DOI: 10.1111/j.1365-4362.1996.tb05057.x
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Immunohistochemical Study of Porokeratotic Eccrine Nevus

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Cited by 15 publications
(10 citation statements)
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“…Punctate porokeratosis is a rare, often congenital variant of porokeratosis which may be clinically indistinguishable from PEODDN. Although punctate porokeratosis is characterized by cornoid lamellation which may involve the sweat gland ostium, hair follicles, or interadnexal epidermis, there are no comedo-like epidermal invaginations (4). PEODDN is characterized by comedo-like epidermal invaginations surrounding cornoid lamellae that emerge exclusively from eccrine ostia.…”
Section: Discussionmentioning
confidence: 99%
“…Punctate porokeratosis is a rare, often congenital variant of porokeratosis which may be clinically indistinguishable from PEODDN. Although punctate porokeratosis is characterized by cornoid lamellation which may involve the sweat gland ostium, hair follicles, or interadnexal epidermis, there are no comedo-like epidermal invaginations (4). PEODDN is characterized by comedo-like epidermal invaginations surrounding cornoid lamellae that emerge exclusively from eccrine ostia.…”
Section: Discussionmentioning
confidence: 99%
“…[2] In recent years, immunohistochemistry with CEA staining the cuticle of the acrosyringium and dermal duct traversing the parakeratotic column but not the inner borders of the epidermal invagination, supports the theory that it represents an abnormally keratinizing epidermal invagination through which an acrosyryngium traverses. [1,5,6] Wang et al, [1] have demonstrated that abnormal keratinizing epidermal invagination may be due to increased proliferation as shown by keratin (Ki-67) staining at the basal layer underneath the cornoid lamella.…”
Section: Case Reportmentioning
confidence: 98%
“…Most patients have relatively localized involvement of an acral site, with 24 of 39 reported cases involving the palms/hands, soles/feet, or both. 1,2,5,7,9,10,13,14,16,18,19,22,27,28,30,[32][33][34][35][36][37][38][39][40][41] The vast majority of PEODDN case reports (32 of 39) describe unilateral involvement, with 7 having bilateral distribution. 6 involving the proximal extremities, trunk, buttocks, neck, or a combination of these has been reported in 13 of 39 cases of PEODDN.…”
Section: Clinical Findingsmentioning
confidence: 99%
“…There have been two prior reports of PEHFN 3,4. Of the 39 total cases of PEODDN, 2 had onset of the disease at birth,1,[5][6][7][8][9]11,13,14,16,18,21,23,24,26, 29-31,33,34,36,39,41 6 had onset in the first few years of life…”
mentioning
confidence: 94%