A yolk sac tumor in a female newborn with a subcutaneous metastasis of the abdominal wall

A. Wacker, F. Neunhoeffer, J. Fuchs, S. Warmann, C. Schwarze, K. Sotlar, H. Scheel-Walter, R. Handgretinger
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引用次数: 3

Abstract

Extragonadal yolk sac tumors (YST) are extremely rare tumors. Only a few case reports can be found in the literature. We report about a female term newborn. After delivery a sacrococcygeal tumor was obvious. Alpha Fetoprotein (AFP) levels were in the upper normal range (91 006 ng/ml). The tumor was completely removed. Histological examinations revealed a typical YST. In the follow-up examinations a subcutaneous metastasis in the abdominal wall was found and excised at the age of 6 weeks. Curative polychemotherapy was induced. After 2 cycles AFP levels were decreased. However, the patient had a local relapse after the 4 cycle of chemotherapy and showed increased AFP levels. Therefore, hyperthermia combined with chemotherapy was applied and a second surgical resection was done. Despite of multiple therapy regime, the patient died due to tumor progress. This case demonstrates an uncommon dissemination of a primary YST. Therapeutic options in neonates are extremely difficult.
女性新生儿卵黄囊肿瘤伴腹壁皮下转移
卵黄囊外肿瘤是一种极为罕见的肿瘤。在文献中只能找到少数病例报告。我们报告一个女性足月新生儿。分娩后骶尾骨肿瘤明显。甲胎蛋白(AFP)水平在正常范围上(91 006 ng/ml)。肿瘤被完全切除了。组织学检查为典型的YST。在随访检查中发现腹壁皮下转移并在6周时切除。诱导多药化疗。2个周期后,甲胎蛋白水平下降。化疗4个周期后局部复发,甲胎蛋白水平升高。因此,采用热疗联合化疗,并进行第二次手术切除。尽管多次治疗,患者仍因肿瘤进展而死亡。本病例显示原发性YST的罕见传播。新生儿的治疗选择非常困难。
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