HAVING MULTIPLE RENAL CYSTS IN A YOUNG ADULT IS
NOT ALWAYS A SIGN OF POLYCYSTIC KIDNEY DISEASE Kaynar K1,*, Kayıpmaz S2, Çebi AH3, Hüseynova Ş4 *Corresponding Author: Professor Dr. Kubra Kaynar, Karadeniz Teknik Üniversitesi, Tıp Fakültesi,
Nefroloji Bilim Dalı, 61080 Trabzon, Turkey. Tel.: +90-542-241-58-79. Fax: +90-462-325-22-70.
E-mail: kkaynar@ yahoo.com page: 1
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INTRODUCTION
Cystic kidney diseases are commonly discovered by
renal imaging methods in adult patients. Simple renal cysts
are the most common (65.0-70.0%) types of all the renal
masses [1]. The incidence of simple renal cysts increase
by aging with an incidence of zero between 15-29 years
of life. Thus, it is especially necessary for young patients
to differentiate the simple cysts from more serious types
such as polycystic kidney disease (PKD), renal abscess,
cystic carcinoma and nephronophthisis. Among these ciliopathies,
a very rarely reported syndrome is cranioectodermal
dysplasia (CED), which should be considered for
young adults, as one of the clinical features of CED is
nephronophthisis [2]. Here, we report a 22-year-old male
patient with multiple bilateral renal cysts finally diagnosed
as CED (or Sensenbrenner syndrome) by genetic testing.
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