1986
Acral persistent papular mucinosis: a new entity
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Cited by 40 publications
(37 citation statements)
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“…The localized variants comprise five subtypes including discrete papular LM, acral persistent papular mucinosis, juvenile and adult variant of self-healing papular mucinosis, papular mucinosis of the infancy and nodular LM [3, 4, 2, 5]. As the morphology of the case reported herein does not fit well into the localized variants as described, we would assign our observation to the third group of the atypical forms of mucinoses.…”
Section: Discussionmentioning
confidence: 72%
“…The localized variants comprise five subtypes including discrete papular LM, acral persistent papular mucinosis, juvenile and adult variant of self-healing papular mucinosis, papular mucinosis of the infancy and nodular LM [3, 4, 2, 5]. As the morphology of the case reported herein does not fit well into the localized variants as described, we would assign our observation to the third group of the atypical forms of mucinoses.…”
Section: Discussionmentioning
confidence: 72%
“…APPM was proposed as a distinct form of cutaneous mucinosis in 1986 [1], and other patients have been reported since in the literature, confirming its easily recog nizable clinical and histological features.…”
mentioning
confidence: 64%
“…In most cases the lesions slowly increase in number but there are no systemic associations [3]. To our knowledge, thirty‐two cases including two from China have been reported earlier [1, 3–26] which strictly agree with the defined diagnostic criteria of APPM [3]. Besides these 32, another six cases reported in the previous century had similar lesions but did not strictly fit the criteria [3].…”
Section: Introductionmentioning
confidence: 78%
