Sanae GHAMMAD, Ghita CHEBİHİ HASSANİ, Fadwa ALLOUCHE, Zineb ALAMİ, Touria BOUHAFA, Khalid HASSOUNİ

Radyoterapi ile tedavi edilen malign retroperitoneal paraganglioma: Olgu sunumu

Paragangliomalar, ilkel nöral krest'in farklılaşmamış hücrelerinden kaynaklanan nadir tümörlerdir. Sol böbreğin sol böbrek üzerinde yer alan geniş retroperitonal tümör hastası olan 33 yaşında bir kadın hastayı sunduk. Serum epinefrin ve norepinefrin düzeyleri yüksek bulundu. Taranmış bir biyopsi yaptık; Histopatolojik inceleme ve immunohistokimyasal analizler retroperitoneal paraganglioma tanısını koydu. Tümör salgılanıp inoperabl olarak değerlendirildi; Bu nedenle radyoterapi ile tedavi edilmeye karar verildi.

Anahtar Kelimeler:

Retroperitoneal paraganglioma, Radyoterapi, Secretory tumor, Pheochromocytoma

Malignant retroperitoneal paraganglioma treated with radiotherapy: A case report

Paragangliomas are rare tumors arising from undifferentiated cells of the primitive neural crest. We report a case of a 33-year-old female patient who presented a large firm retroperitoneal tumor situated on the left flank above the left kidney. Levels of the serum epinephrine and norepinephrine were high. We performed a scanned biopsy; the histopathological examination and the immunohistochemical analyses concluded the diagnosis of a retroperitoneal paraganglioma. The tumor was judged secreting and inoperable; therefore it was decided to be treated with radiotherapy.

Keywords:

Retroperitoneal paraganglioma, Radiotherapy, Secretory tumor, Pheochromocytoma,

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