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Cronkhite–Canada Syndrome: Dermatological Features

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Atlas of Dermatological Manifestations of Gastrointestinal Disease
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Abstract

Clinical signs and features include:

Dermatological triad:

1. Hyperpigmentation: macules and papules (lentigo-like), light to dark brown, a few mm to 10 cm in diameter, diffusely located but most commonly on the hands, feet, face, lips, buccal mucosa

2. Nail changes: dystrophy, onycholysis, unique inverted triangle of inverted normal nail bordered by dystrophic nail.

3. Alopecia: rapidly progressive, patchy but leading to complete hair loss: also facial, axillary, extremity, and pubic hair loss.

Median age diagnosis, 59 years old.

Males > females

Since 1955, there have been 400 cases, 75 % in Japan, 15 % develop malignancy most commonly of the sigmoid colon and rectum.

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References

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  4. Herzberg AJ, Kaplan DL. Cronkhite-Canada syndrome: light and electron microscopy of the cutaneous pigmentary abnormalities. Int J Dermatol. 1990;29:121–5.

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Correspondence to Liam Zakko .

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Zakko, L., Finch, J., Rothe, M.J., Grant-Kels, J.M. (2013). Cronkhite–Canada Syndrome: Dermatological Features. In: Wu, G., Selsky, N., Grant-Kels, J. (eds) Atlas of Dermatological Manifestations of Gastrointestinal Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-6191-3_60

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  • DOI: https://doi.org/10.1007/978-1-4614-6191-3_60

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