Malignant retroperitoneal paraganglioma treated with radiotherapy: A case report

Year 2019, , 105 - 108, 27.01.2019

Sanae Ghammad , Ghita Chebihi Hassani Fadwa Allouche , Zineb Alami Touria Bouhafa Khalid Hassouni

https://doi.org/10.28982/josam.456705

Abstract

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

Radyoterapi ile tedavi edilen malign retroperitoneal paraganglioma: Olgu sunumu

Abstract

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.

Keywords

Retroperitoneal paraganglioma, Radyoterapi, Secretory tumor, Pheochromocytoma

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