1986
DOI: 10.1001/archderm.1986.01660130086032
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Elastosis Perforans Serpiginosa in a Patient With Renal Disease

Abstract: We encountered a case of elastosis perforans serpiginosa in a patient with coexisting renal disease, the first such reported association of which we are aware. The perforating disorders tend to have atypical clinical features when associated with renal disease. The exact pathogenic mechanism by which renal disease predisposes to a perforating disease remains to be elucidated but is likely to be related to minor trauma, which occurs in renal disease.

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Cited by 25 publications
(9 citation statements)
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“…In the primary perforating disorders, an interaction between elastin and its receptor on keratinocytes in elastosis perforans serpingiosa 39 and an overexpression of TGF‐β 3 in reactive perforating collagenosis 40 have been described. For the acquired perforating dermatoses, several pathomechanisms have been proposed and include a possible pathogenetic role for fibronectin, 41,42 microtrauma associated with chronic pruritis and scratching, 43–45 abnormal vitamin A or vitamin D 46 metabolism, hypoxic skin conditions 47 and diabetes‐related microangiopathy 45 …”
Section: Discussionmentioning
confidence: 99%
“…In the primary perforating disorders, an interaction between elastin and its receptor on keratinocytes in elastosis perforans serpingiosa 39 and an overexpression of TGF‐β 3 in reactive perforating collagenosis 40 have been described. For the acquired perforating dermatoses, several pathomechanisms have been proposed and include a possible pathogenetic role for fibronectin, 41,42 microtrauma associated with chronic pruritis and scratching, 43–45 abnormal vitamin A or vitamin D 46 metabolism, hypoxic skin conditions 47 and diabetes‐related microangiopathy 45 …”
Section: Discussionmentioning
confidence: 99%
“…Over the last two decades, the four major perforating disorders have also been observed in adult patients with CRF and/or DM as well as some other systemic disorders. The authors of these reports used many confusing terms such as EPS, 15 acquired RPC, 16 reactive perforating collagenosis of DM and renal failure, 17 PF, 14 PF of haemodialysis, 18 KD, 19 Kyrle‐like lesions, 20 uremic follicular hyperkeratosis, 21 and perforating pseudoxanthoma elasticum 22 . Later on, because of the close clinical and histopathological resemblance among these cases, it was suggested that they are the variants of the same disease process 23 .…”
Section: Discussionmentioning
confidence: 99%
“…Perforating folliculitis (2) c. Blastomycosis (13) c. Amyloid (13) 5. Secondary to CRF and/or DM (2,(52)(53)(54)(55)(56)(57)(58)(59) d. Cryptococcosis (13) d. Ochronotic pigment (25) e. Leischmaniasis (13) e. Elastic fibres (12, 16) f. Histoplasmosis (17) f. Steroids (15) 31 May 1998. Three-mmthick sections were cut from archival paraffin wax blocks and stained with haematoxylin and eosin (H& E), giemsa and silver (Warthin Starry) stains.…”
Section: Methodsmentioning
confidence: 99%