Two brothers with confluent and reticulated papillomatosis

Rietz, Stephan; Grabbe, Stephan; Stebut, Esther von

doi:10.1111/ddg.12982

Cited by 5 publications

(6 citation statements)

References 4 publications

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“…In this study we report two identical twin sisters with CRP diagnosis. Few cases of the disease in the same family between siblings have been reported in the literature [6,7]. However, no case of identical twin sisters has been reported.…”

Section: Discussionmentioning

confidence: 99%

Confluent and Reticulated Papillomatosis of Gougerot and Carteaud in Two Identical Twins: Case Report

Malveira¹,

Dornelas²,

Leite³

et al. 2020

SCR

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Confluent and reticulated papillomatosis of Gougerot-Carteaud (CARP) is a rare dermatosis. Even though many authors affirm that it is a keratinization disorder, the causes are still unknown. There are various therapeutic options to treat this disorder: retinoids, antibiotics, keratolytic, and others, but the results are unsatisfactory. This study presents the case of two identical twins, approaching clinic characteristics, as well as histopathologic characteristics, and the difficulties of finding the correct diagnosis since it is a rare disease.

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Section: Discussionmentioning

confidence: 99%

Confluent and Reticulated Papillomatosis of Gougerot and Carteaud in Two Identical Twins: Case Report

Malveira¹,

Dornelas²,

Leite³

et al. 2020

SCR

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“…This is the largest case series of patients with familial CRP. There has been a total of 9 kindreds reported in the literature, all of which described only 2 4-10 or 3 family members. 11,12…”

Section: Discussionmentioning

confidence: 99%

“…[2][3][4] Familial predisposition has been suggested. [4][5][6][7][8][9][10][11][12] We report 2 kindreds of CRP, including 4 family members over 3 generations.…”

mentioning

confidence: 99%

Familial Confluent and Reticulated Papillomatosis in 2 Kindreds Including 3 Generations

Berg

Pehr

2018

J Cutan Med Surg

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“…as a familial occurrence suggesting a genetic predisposition [5]. Still there is no consensus on the pathogenic mechanisms that lead to this puzzling but treatable distinct entity [6].…”

Section: Clinical Lettermentioning

confidence: 99%

Papillomatosis confluens et reticularis (Morbus Gougerot‐Carteaud) – a retrospective study of 25 patients

Weins

Biedermann

Mempel

et al. 2021

J Deutsche Derma Gesell

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Papillomatosis confluens et reticularis (Morbus Gougerot-Carteaud) -a retrospective study of 25 patients Dear Editors, Papillomatosis confluens et reticularis (Morbus Gougerot-Carteaud; MGC) is a poorly understood skin disorder predominantly affecting adolescents and young adults [1]. Patients typically show brownish, reticular coalescing papules and plaques with predilection of the neck, upper trunk and axillae (Figure 1) [1-3]. Given its nonspecific histopatho-

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Two brothers with confluent and reticulated papillomatosis

Cited by 5 publications

References 4 publications

Confluent and Reticulated Papillomatosis of Gougerot and Carteaud in Two Identical Twins: Case Report

Confluent and Reticulated Papillomatosis of Gougerot and Carteaud in Two Identical Twins: Case Report

Familial Confluent and Reticulated Papillomatosis in 2 Kindreds Including 3 Generations

Papillomatosis confluens et reticularis (Morbus Gougerot‐Carteaud) – a retrospective study of 25 patients

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