睾丸畸胎瘤向原始神经外胚层肿瘤的恶性转化。

IF 0.7 Q4 UROLOGY & NEPHROLOGY Urology Annals Pub Date : 2022-10-01 DOI:10.4103/ua.ua_162_21
Daniyah Elagi, Rodney Young, Abdulmajeed Dayili
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引用次数: 0

摘要

畸胎瘤是一种影响年轻成年男性的常见生殖细胞肿瘤。少数睾丸畸胎瘤有沿内胚层、外胚层或中胚层线恶性转化的潜力。我们报告的转移性混合生殖细胞肿瘤由原始神经外胚层肿瘤(PNET)合并成熟畸胎瘤组成。PNET是一种高度侵袭性肿瘤,对标准铂基化疗反应差,预后差。PNET的主要治疗方法是手术切除。畸胎瘤向PNET恶性转化是一种罕见的现象。文献中仅有少数畸胎瘤向PNET恶性转化的病例报道。在此,我们报告一例罕见的PNET病例,发生于恶性混合生殖细胞肿瘤,患者为23岁男性,他接受了阿霉素、环磷酰胺(VAC)、异环磷酰胺和依托泊苷(IE)交替化疗和腹膜后淋巴结切除术。
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Malignant transformation of testicular teratoma to primitive neuroectodermal tumor.

Teratoma is a common germ cell tumor that affects young adult males. A small number of testicular teratomas have the potential for malignant transformation along endodermal, ectodermal, or mesodermal lines. The metastatic mixed germ cell tumor we reported consists of the primitive neuroectodermal tumor (PNET) with mature teratoma. PNET is a highly aggressive tumor with a poor prognosis given its poor response to standard platinum-based chemotherapy. The primary treatment for PNET is surgical resection. Malignant transformation of teratoma to PNET is a rare phenomenon. Only a few cases of malignant transformation of teratomas to PNET are reported in the literature. Here, we present a rare case of PNET arising in a malignant mixed germ cell tumor in a 23-year-old male who underwent adjuvant adriamycin, cyclophosphamide (VAC) alternating with ifosfamide and etoposide (IE) chemotherapy and retroperitoneal lymph node dissection.

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来源期刊
Urology Annals
Urology Annals UROLOGY & NEPHROLOGY-
CiteScore
1.20
自引率
0.00%
发文量
59
审稿时长
31 weeks
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