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Ewing's Sarcoma (Primitive Neuroectodermal Tumor) of Seminal Vesicles: A Case Report
被引:1
|作者:
Badheeb, Ahmed M.
[1
,2
]
Alshukami, Anwar A.
[3
]
Bashanfer, Galal A.
[4
]
Alkhanbashi, Omar M.
[5
]
Badheeb, Mohamed A.
[6
]
机构:
[1] King Khalid Hosp, Oncol Ctr, Najran, Saudi Arabia
[2] Hadhramout Univ, Med, Mukalla, Yemen
[3] King Khalid Hosp, Diagnost Radiol, Najran, Saudi Arabia
[4] King Khalid Hosp, Pathol & Lab Med, Najran, Saudi Arabia
[5] King Khalid Hosp, Urol, Najran, Saudi Arabia
[6] King Khalid Hosp, Gen Med, Najran, Saudi Arabia
关键词:
extra-skeletal ewing sarcoma;
ewing sarcoma (es);
primitive neuroectodermal tumor (pnet);
seminal vesicle;
seminal vesicle ewing sarcoma;
TERM-FOLLOW-UP;
BONE;
FAMILY;
D O I:
10.7759/cureus.21993
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Malignant tumors of the seminal vesicles are rare; they may he of epithelial or mesenchymal origin. Carcinomas are the most common and pelvic sarcoma may he confused with a primary tumor of the seminal vesicles. Little is known of the prognosis and best sequence of treatment in such sarcoma. We report a rare case of extra-skeletal Ewing sarcoma/primitive neuroectodermal tumor of the seminal vesicles in a 54-year-old man who presented with chronic lower abdominal pain, urinary retention, and severe constipation. Pelvic CT scan and MRI confirmed the presence of a soft tissue mass lesion centered on seminal vesicles. A trans-gluteal Tru-cut biopsy confirmed the diagnosis. Three cycles of the preoperative chemotherapy VAC/JE (vincristine, Adriamycin and cyclophosphamide, followed by ifosfamide and etoposide) protocol achieved an excellent clinical response.
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