Updated Diagnosis Criteria for Confluent and Reticulated Papillomatosis: A Case Report

Jo, Seongmoon; Park, Hyun Sun; Cho, Soyun; Yoon, Hyun Sun

doi:10.5021/ad.2014.26.3.409

Cited by 16 publications

(15 citation statements)

References 5 publications

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“…The trunk, particularly the intermammary areas, epigastrium, and back, is the most common region affected. Recent observations of CRP on the face, axilla, and groin have also been reported …”

Section: Discussionmentioning

confidence: 83%

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Punctate, pigmented, and verrucous papillomatosis: a rare variant of Gougerot–Carteaud syndrome

Ibekwe

Ukonu

2015

Int J Dermatology

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Section: Discussionmentioning

confidence: 83%

“…Recent obser-vations of CRP on the face, axilla, and groin have also been reported. 3,6,7 Histology of the three different cutaneous papillomatoses described by Gougerot and Carteaud is indistinguishable. 1 Characteristically, they have demonstrated hyperkeratosis, papillomatosis, and acanthosis.…”

Section: Discussionmentioning

confidence: 93%

Punctate, pigmented, and verrucous papillomatosis: a rare variant of Gougerot–Carteaud syndrome

Ibekwe

Ukonu

2015

Int J Dermatology

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“…Die Rolle von Pityrosporon ovale in PCR-Läsionen dagegen wurde in den letzten Jahren zwar als pathogenetisch relevant beschrieben, ist jedoch seit kurzem in die Diskussion geraten, da nur in einem geringen Teil der PCR-Läsionen diese Hefe nachgewiesen wurde [46]. Therapeutisch wirksam ist interessanterweise Minocyclin [47], was ebenso die bakterielle These stützt.…”

Section: Merkeunclassified

“…Analog zur AN wird auch die PCR gehäuft bei Patienten mit Diabetes mellitus, Adipositas, aber auch Amyloidose beobachtet [46]. Klinische Diagnosekriterien umfassen den klinischen Befund bräunlicher Maculae und Plaque mit retikulärem Muster, welche den oberen Stamm, Hals und die Flexuren betreffen, fehlender Nachweis von Pilzen sowie fehlendes Ansprechen auf antimykotische Therapien, hingegen jedoch wie erwähnt exzellentes Ansprechen auf eine antibiotische Therapie (Minocyclin) [47].…”

Section: Merkeunclassified

Erworbene retikuläre Pigmentdermatosen

Müller¹,

Vogt²

2019

Akt Dermatol

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Clinical differential diagnoses of acquired hyperpigmentation of the skin are manifold. The rarity and fuzzy demarcation between various entities on the one hand and the alleged insignificance and harmlessness of the dermatoses on the other hand often delay a rapid diagnosis in everyday clinical practice. In the present work the most important clinical differential diagnoses are reviewed. Acquired reticular pigment dermatoses (RPD) of the skin sui generis include Dowling-Degos disease (DDD), Galli-Galli disease (GGD). Further diseases rarely found in Europe are Kitamura disease (RKD), reticular acropigmentation Dohi (RAD) and Haber syndrome (HS). Other acquired more frequent hyperpigmentation of the skin, which may also have a reticular pattern, include acanthosis nigricans, papillomatosis confluens et reticularis Gougerot carteaud, diabetic dermatopathy, and postinflammatory hyperpigmentation. Some of these diseases are particularly indicative of endocrinopathies. In particular, childhood acanthosis nigricans is of great importance in diabetes mellitus screening. Histopathological examination with the clinical problem of acquired hyperpigmentation can be difficult and requires close clinical-pathological correlation.

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“…Given that topical isotretinoin treatment initially led to improvement in a hyperkeratotic test area on the trunk, we started the patient on topical isotretinoin 1-2 times daily. However, no further improvement was achieved over the to either azithromycin or local treatment with fusidic acid, and not to antiinflammatory agents or drugs that affect epidermal differentiation, however, strongly support the contributing role of gram-positive bacteria (e. g. Dietzia papillomatosis [11][12][13][14]) in the development of the disease. course of several weeks.…”

mentioning

confidence: 96%