RESUMO
Juvenile granulosa cell tumor [JGCT] is one of the rare sex cord-stromal tumours of the ovary occurring in the first two decades of life .It makes less than 5% of ovarian tumours in childhood and adolescence
It is different from adult granulosa cell tumor that is seen in older females with respect to clinical and pathological features as well as biological behaviour. In this article we report a case of juvenile granulosa cell tumor of the right ovary in a 7-month-old infant which was presented with vaginal bleeding
RESUMO
Rhabdomyosarcoma of biliary tract system [RMS/BT] is a very rare form of RMS that usually presents with jaundice in young children. In some rane cases icter disappears transiently and causes delay in diagnosis, there fore this condition must be included in differential diagnosis of obstructive jaundice in infants and children
Ultrasonography is very useful for diagnosis of abdominal mass and clarifying it's relationship with the biliary tract system. Surgery is critical for estabilishing accurate diagnosis and determining the extent of regional disease, but aggressive surgery is not recommended because, despite gross residual mass after surgery the outcome of chemotherapy +/- radiotherapy is sufficient. Because this tumor is very rare and its treatment has improved in recent years we report a case of RMS/BT in a 15-month girl who presented with abdominal mass and history of obstructive jaundice