Rapid Regrowth of Atypical Teratoid Rhabdoid Tumor after Gross Total Resection in Adult: Case Report

Jun Mo Kim, Gwang Yoon Choi, K. Choi, H. Choi
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Abstract

Atypical teratoid/rhabdoid tumors (AT/RTs) are rare embryonal tumors. Herein, we present an unusual case of an AT/RT showing rapid regrowth to more than its original size approximately 1 month after gross total resection (GTR). A 22-year-old man presented with a severe headache. On magnetic resonance imaging (MRI), a tumor was found in the left cerebellopontine angle (2.8 × 3.7 × 3.7 cm; 38.3 cm 3 ). GTR was performed, and biopsy confirmed AT/RT. On day 38 after surgery, a follow-up MRI due to abrupt mental deterioration to coma was performed, showing that the tumor had regrown to be even larger than its original size (3.6 × 3.5 × 5.3 cm; 66.78 cm 3 ). After 1 month, the patient died. The median survival of AT/RT patients who undergo GTR is 20 months. In our case, the patient died much earlier than the previously reported overall survival duration after GTR. Therefore, physicians should always be wary of the possibility of rapid regrowth of AT/RTs when establishing the treatment plan.
成人非典型畸胎体样横纹肌瘤全切除后快速再生1例
非典型畸胎瘤/横纹肌样瘤是一种罕见的胚胎性肿瘤。在此,我们报告一个不寻常的AT/RT病例,显示在总全切除(GTR)后大约1个月快速再生到超过其原始大小。一名22岁男子表现为严重头痛。MRI示左侧桥小脑角(2.8 × 3.7 × 3.7 cm;38.3厘米3)。行GTR,活检证实为AT/RT。术后第38天,因突然精神恶化致昏迷的随访MRI显示肿瘤已再生,甚至比原来的大小更大(3.6 × 3.5 × 5.3 cm;66.78厘米3)。1个月后,患者死亡。接受GTR的AT/RT患者的中位生存期为20个月。在我们的病例中,患者的死亡时间远远早于先前报道的GTR后的总生存时间。因此,医生在制定治疗方案时应始终警惕AT/RTs快速再生的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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