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Papillary pineocytoma in child: a case report

W. Marcol, K. Kotulska, W. Grajkowska, D. Gołka, P. Właszczuk, M. Drogosiewicz, M. Mandera, J. Lewin-Kowalik, M. Roszkowski

. 2007 ; 151 (1) : 121-123.

Jazyk angličtina Země Česko

Typ dokumentu kazuistiky, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc13003626

BACKGROUND: Papillary pineocytoma is an extremely rare tumor usually with a poor outcome. CASE REPORT: We report a case of a 10-year-old-girl with pineal gland tumor and obstructive hydrocephalus diagnosed using MRI. The child was successful treated by insertion of a ventriculoperitoneal shunt and consecutive tumor resection by supracerebellar-infratentorial approach. Histopathological examination showed a papillary structure of the pineocytoma. As such, tumors are considered to be aggressive the child was subjected to radio- and chemotherapy. CONCLUSION: At six year follow-up after surgery, the patient is symptom-free and the MRI shows no tumor recurrence.

Citace poskytuje Crossref.org

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$a Grajkowska, Wiesława $u Department of Pathology, The Children's Memorial Health Institute, Warsaw, Poland
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$a Gołka, Dariusz $u Department of Pathology, Medical University of Silesia, Katowice, Poland
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