1,720,983 research outputs found
Berthold von Moosburg, Expositio super elementationem theologicam Procli, Sach- und Quellenregister
Su di un caso di meningioma del Tuberculuim Sellae: manifestazioni oculari e problemi di diagnosi differenziale
Un nuovo trattamento nella terapia del Calazio: l’iniezione intraparenchimale di corticosteroidi
Distacco di retina bilaterale in corso di eclampsia gravidica: documentazione fluoroangiografica e considerazioni patogenetiche
Single and combined deactivating effect of alkali metals and HCl on commercial SCR catalysts.
Studio Ecografico A-scan degli esoftalmi non tiroidei, osservati nella Clinica Oculistica di Siena nel bioennio: 1979-1980
A case of primary botryoid conjunctival rhabdomyosarcoma
Background: Rhabdomyosarcoma is the most common childhood primary orbital malignancy, but the occurrence of this tumour in the conjunctiva is rare. Methods: A 14-year-old girl presented with a visible case of conjunctival mass in the left eye. The year before, the patient was referred to another hospital for a biopsy of a conjunctival mesenchymal tumour in the same site, which was periodically checked after the excision. We intervened by partially removing the conjunctival mass. Results: The histopathology revealed a botryoid rhabdomyosarcoma. The patient underwent chemotherapy and fractionated radiotherapy. The follow-up after three years revealed that the patient remained clinically tumor-free, with no ocular complication from the radiotherapy. Conclusions: It is evident that by not excising the tumour in its entirety it is therefore possible to preserve the underlying rectus muscles and not interfere with ocular motility. Subsequent radiotherapy and chemotherapy helped to destroy any residual tumour. Alternatively, surgical excision of the mass alone could lead to recurrence of the tumour after some months or years
Indagine clinico-statistica sui portatori di lenti a contatto nell’ambulatorio della Clinica Oculistica di Siena
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