TITLE:
Rothmund-thomson syndrome and cutan T-cell lymphoma in childhood
AUTHORS:
Katalin Bartyik, K. Míta Gábor, Béla Iványi, István Németh, Eszter Karg
KEYWORDS:
Rothmond Thomson Syndrome; Genetic Disorder; Cutan T-Cell Lymphoma
JOURNAL NAME:
Open Journal of Pediatrics,
Vol.3 No.3,
August
29,
2013
ABSTRACT: We
report a 3-year-old girl suffering from RothmundThomson
Syndrome (RTS). The patient at birth had multiplex anomalies:
poikilodermatous rash, sceletal abnormalities:
palatoschisis, micrognathi, aplasia radii, hypoplastic right and left thenar and thumbs, pesequinus on both site,
ectopy renis. The patient in the later ages was detected dental malformation,
facial dysmorfism. At the age 3, she had lasion in her muscle. After biopsy,
histological examination showed cutan T-cell lymphoma. The patient is the first
case who had cutan T-cell lymphoma associated with RTS in this young age.