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Multiple perforating and non perforating pilomatricomas in a patient with Churg–Strauss syndrome and Rubinstein−Taybi syndrome

Authors


* Corresponding author, P Bayle, Place du Baylac, Toulouse Cedex, 31059, tel: +5 6177 9494; fax: +5 6177 7430; E-mail: bayle.p@chu-toulouse.fr

SUMMARY

We report an unusual association of multiple perforating and non-perforating pilomatricomas with Churg–Strauss syndrome, and a dysmorphic syndrome evocative of Rubinstein-Taybi syndrome. These syndromes may be independent, but these rare diseases and genetic abnormalities may be linked together.

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