The clinical case of Sneddon - Wilkinson disease in a pregnant woman

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Abstract


Describes a rare clinical case demonstrating the sudden appearance of the disease Sneddon - Wilkinson in women during pregnancy, which regressed completely within a month after birth and had no recurrence.

About the authors

M. S. Askhakov

Stavropol State Medical University

Author for correspondence.
Email: kedri2007@yandex.ru

Russian Federation

V. V. Chebotarev

Stavropol State Medical University

Email: kedri2007@yandex.ru

Russian Federation

A. V. Odinec

Stavropol State Medical University

Email: kedri2007@yandex.ru

Russian Federation

References

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  2. Berk D., Hurt M., Mann C., Sheinbein D. Sneddon - Wilkinson disease treated with etaner-cept: report of two cases. Clin Exp Dermatol 2009; 34 (3): 347-51.
  3. Lombart F., Dhaille F., Lok C., Dadban A. Subcorneal pustular dermatosis associated with Mycoplasma pneumoniae infection. J Am Acad Dermatol 2014; 71 (3): e85-e86.
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  7. Nievas M., Pugnaire M., Salmeron M., Lora V. Patient with subcorneal pustular dermatosis: Sneddon-Wilkinson syndrome. J Am Acad Dermatol 2013; 68 (4): AB57-AB57.
  8. Lew T., Hague J., Colloby P., Oripin S. Sneddon-Wilkinson disease associated with seronegative inflammatory polyarthritis. J Am Acad Dermatol 2012; 66 (4): AB61-AB61.

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