2014
DOI: 10.1111/jdv.12542
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Regional lymphomatoid papulosis in association with pseudoepitheliomatous hyperplasia: 13 years follow‐up

Abstract: mucosal lesions, 5,6 the handheld device seems to improve the access to difficult areas.In conclusion, our two cases support the possible application and usefulness of RCM for confirmation of inflammatory mucosal diseases, excluding tumoural processes and orienting the biopsy site selection. More advanced experiences on different oral mucosa diseases, also involving deeper areas of the oral cavity, are needed to demonstrate the effective usefulness of the handheld RCM in oral diseases diagnosis and patient man… Show more

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Cited by 5 publications
(3 citation statements)
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References 8 publications
(13 reference statements)
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“…Nevertheless, careful histologic examination revealed no keratinocyte atypia. Pseudoepitheliomatous hyperplasia in lesions of LyP have been reported in adults in small case series, but rarely in pediatric patients 16,17. Its occurrence, however, has no significant difference in clinical outcome or prognosis.…”
Section: Discussionmentioning
confidence: 98%
See 1 more Smart Citation
“…Nevertheless, careful histologic examination revealed no keratinocyte atypia. Pseudoepitheliomatous hyperplasia in lesions of LyP have been reported in adults in small case series, but rarely in pediatric patients 16,17. Its occurrence, however, has no significant difference in clinical outcome or prognosis.…”
Section: Discussionmentioning
confidence: 98%
“…Pseudoepitheliomatous hyperplasia in lesions of LyP have been reported in adults in small case series, but rarely in pediatric patients. 16,17 Its occurrence, however, has no significant difference in clinical outcome or prognosis. Keratoacanthomas have also been reported to occur in older patients with LyP and has not been reported in pediatric patients.…”
Section: Discussionmentioning
confidence: 99%
“…Overlapping cases with more than one subtype in a single case have also been reported [14]. Less common variants such as folliculotropic (F subtype), [15,16], syringotropic, spindle cell, angioinvasive, pseudoepitheliomatous, intralymphatic, and granulomatous eccrinotropic [17][18][19][20][21][22] are not yet listed in the official WHO classification. Unfortunately, there is no established correlation between histopathologic subtypes and clinical presentation, apart from type E which includes eschar-like necrosis [2,23].…”
Section: Introductionmentioning
confidence: 99%