Embryonal Rhabdomyosarcoma of Upper Lid in 15-Year-Old Patient

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منابع مشابه

Embryonal Rhabdomyosarcoma of Upper Lid in 15-Year-Old Patient

Rhabdomyosarcoma is the most common childhood primary malignant tumor of orbit. Most of patients present between the ages of 7 and 8 years. Pure eyelid rhabdomyosarcoma is a very rare tumor with only a few reported cases in the literature. We introduce a pure embryonal rhabdomyosarcoma of upper lid in 15-year-old patient and demonstrate successful management of it.

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Fetal rhabdomyomas (RM) are extremely rare benign mesenchymal tumours that occur primarily in the head and neck.This tumour exhibits immature skeletal muscle differentiation. The patients’ median age is four years and surgical resectionis the recommended treatment.Fetal RM of limbs are rare and not well described in the literature and if, predominantly in form of case reports. We reportthe seco...

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A Case of Embryonal Rhabdomyosarcoma of Cervix Uteri in a 14 Year Old Girl

Rhabdomyosarcoma is an aggressive soft tissue malignancy of childhood and adolescence arising from embryonal mesenchyme [1]. As compared to literature available, these tumours are mainly discussed in context of case studies. Most common affected sites are head, neck, abdomen and genitourinary tract [2]. Embryonal rhabdomyosarcoma is the most common subtype, of which botryoid is a polypoidal var...

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Embryonal rhabdomyosarcoma of the caruncle in a 4 year-old boy: case report.

Rhabdomyosarcoma is a rare tumor, with an annual incidence of 4.3 cases per million children. Even thought, it is the most common soft tissue sarcoma in childhood, with a mean age of 6 to 8 years at diagnosis. A 4 year-old boy presented with a history of a fast growing (1-month) nodular lesion in the caruncle of his left eye. Slit lamp examination showed a vascularized solid nodular lesion in t...

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Rhadomyosarcoma is the most common tumour of the soft tissues in infants and children. We report a case of a 3 1/2 year old girl who presented with a swelling over the neck. Swelling was diagnosed as Rhabdomyosarcoma (embryonal type). Tumour mass was found to be unresectable initially. The patient was subjected to multiple courses of checmotherapy, which shrunk the tumour significantly. There w...

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ژورنال

عنوان ژورنال: Case Reports in Ophthalmological Medicine

سال: 2014

ISSN: 2090-6722,2090-6730

DOI: 10.1155/2014/157053