1.Relapsed Wilms' tumor with multiple brain metastasis.
Akın AKAKIN ; Baran YILMAZ ; Murat Sakir EKŞI ; Ozlem YAPICIER ; Türker KILIÇ
Korean Journal of Pediatrics 2016;59(Suppl 1):S96-S98
Wilms' tumor is the most common malignant renal tumor in childhood. The brain metastasis of a Wilms' tumor with anaplastic histopathology is rare. We present the case of an 8-year-old girl with Wilms' tumor, who presented with multiple brain metastases 5 years after her primary diagnosis. The brain masses were diagnosed after a generalized tonic-clonic seizure attack. The big solid mass in the cerebellum was resected, and whole-brain radiotherapy was performed, after which, she succumbed to her disease. In the case of clinical suspicion, cranial surveillance should be included in the routine clinical work-up for Wilms' tumor. Combined aggressive therapy (surgery+radiotherapy+chemotherapy) should be applied whenever possible, for both better survival and palliative aspects.
Brain*
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Cerebellum
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Child
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Diagnosis
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Drug Therapy
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Female
;
Glycogen Storage Disease Type VI
;
Humans
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Neoplasm Metastasis*
;
Radiotherapy
;
Seizures
;
Wilms Tumor*
2.Concomitant Double Tumors of Myxopapillary Ependymoma Presented at Cauda Equina-Filum Terminale in Adult Patient.
Ulaş YENER ; Mustafa GÜDÜK ; Murat Sakir EKŞI ; Murat Hamit AYTAR ; Aydın SAV ; Serdar ÖZGEN
Korean Journal of Spine 2016;13(1):33-36
A 32-year-old man presented with gradually increasing bilateral buttock pain. He had intermittent claudication. Multiple, homogenously enhanced intradural extramedullary lesions at L2-L3 and L5-S1 levels were observed on magnetic resonance imaging. The tumors were debulked and were removed in piecemeal pattern until they had completely been resected. Histopathological examination of the surgical specimens confirmed that both tumors were myxopapillary ependymomas (MPE). MPE presenting as concomitant double tumor at conus-cauda-filum level are very rare. This kind of presentation could not be directly considered as dissemination, since both tumors were in the site of classical origin of MPE. Ten cases of double spinal MPEs have been reported to date. Including the present case, analysis of the 11 patients revealed some facts. There is a male predominance, which is opposite to the ependymomas that are commonly observed in females. Median age at presentation is 15 years. Most pronounced symptom is low back pain that sometimes radiates to lower extremities. Surgical approach was aimed in all tumors, which could be succeeded in all tumors except one. Adjuvant radiation therapy was applied in 5 patients. No recurrences have been reported after surgery or surgery + radiotherapy regimens.
Adult*
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Buttocks
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Ependymoma*
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Female
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Humans
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Intermittent Claudication
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Low Back Pain
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Lower Extremity
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Magnetic Resonance Imaging
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Male
;
Radiotherapy
;
Recurrence