睾丸生殖细胞瘤腹膜后淋巴结清扫术后单侧手臂无力。

IF 0.8 Q3 ANESTHESIOLOGY Anaesthesia reports Pub Date : 2024-07-10 DOI:10.1002/anr3.12312
S. Gaikwad, B. Trivedi, S. Gholap
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引用次数: 0

摘要

一名 26 岁的男子被诊断为非肉芽肿性睾丸生殖细胞瘤,随后接受了腹膜后淋巴结清扫术。此前,他曾接受过腹股沟睾丸切除术。手术在全身麻醉和胸腔硬膜外镇痛下进行。手术开始四小时后,患者出现心动过速和低血压,输液治疗无效。因此,开始静脉注射去甲肾上腺素,剂量为 0.01-0.07 μg.kg-1.min-1,术后 2 小时停止。手术过程中,双臂外展至 90 度。手术结束后,患者的气管被拔除,并被转入重症监护室。术后第一天,患者出现左上肢单瘫,无感觉障碍。患者接受了脑部和臂丛磁共振成像(MRI)检查。脑部核磁共振成像显示出血性病变,周围水肿,诊断为无症状瘤内出血,颅内压升高(图 1)。由于该病灶界限清楚且为单发,因此被怀疑为转移性病灶。睾丸肿瘤可以转移到脑部,但这种情况很少见。患者接受了静脉注射地塞米松治疗,并接受了靶向放疗,术后第21天手臂无力症状完全恢复。非肉芽肿性睾丸生殖细胞瘤的脑转移并不常见,但更可能发生在40岁以上、β-人绒毛膜促性腺激素(≥ 5000 IU.l-1)和甲胎蛋白(> 10,000 ng.ml-1)水平升高、肺转移或骨转移以及出现神经系统症状的患者身上。由于没有这些症状且肿瘤标志物水平较低,该病例没有进行术前脑部成像[1, 2]。在非肉芽肿性睾丸生殖细胞瘤中,自发性肿瘤出血非常罕见,虽然患者的凝血功能和血小板正常,但全身免疫反应综合征和免疫抑制可能是导致出血风险的原因之一。全身免疫反应综合征可能会导致新陈代谢和血管并发症的增加,可能会影响瘤内出血的发生[3, 4]。对我们来说,关键的一点是脑转移瘤可能会模拟麻醉并发症,如臂丛神经损伤或脑血管意外。这凸显了在术后进行全面鉴别诊断的必要性,以确保准确识别和处理潜在疾病。
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Unilateral arm weakness following retroperitoneal lymph node dissection for testicular germ cell tumour

A 26-year-old man underwent retroperitoneal lymph node dissection following diagnosis of non-seminomatous testicular germ cell tumour. He had previously undergone an inguinal orchidectomy. The surgery was performed under general anaesthesia with thoracic epidural for analgesia. Four hours after the start of surgery, tachycardia and hypotension developed which did not respond to fluid therapy. Therefore, intravenous noradrenaline infusion was started at a rate of 0.01–0.07 μg.kg−1.min−1 which was discontinued 2 h after surgery. During the operation, both arms were abducted to 90 degrees. At the end of the surgery, the patients' trachea was extubated and he was transferred to the intensive care unit. On the first postoperative day, the patient developed a left upper limb monoparesis without sensory deficit. Magnetic resonance imaging (MRI) of the brain and brachial plexus were undertaken. The MRI brain revealed a haemorrhagic lesion with surrounding oedema, leading to a diagnosis of symptomatic intratumoural bleed with raised intracranial pressure (Fig. 1). This was suspected to be a metastatic lesion as it was well-defined and solitary. Testicular tumours can metastasise to the brain, although this is rare. The patient was treated with intravenous dexamethasone and received targeted radiotherapy which led to complete recovery of the arm weakness by postoperative day 21.

Brain metastases in non-seminomatous testicular germ cell tumours are uncommon, but more likely to occur in those over 40, with elevated levels of β-human chorionic gonadotropin (≥ 5000 IU.l−1) and alpha-fetoprotein (> 10,000 ng.ml−1), pulmonary or bone metastases, and neurological symptoms. Due to the absence of these symptoms and low tumour marker levels, pre-operative brain imaging was not performed in this case [1, 2]. The tumour markers were repeated and were within normal range.

In non-seminomatous testicular germ cell tumours, spontaneous tumour bleed is rare, and while the patient's coagulation profile and platelets were normal, systemic immune response syndrome and immune suppression may have contributed to the bleeding risk. Systemic immune response syndrome may lead to increased metabolism and vascular complications, possibly influencing the occurrence of intratumoural bleeding [3, 4].

For us, the key point is that brain metastases can mimic anaesthetic complications, such as brachial plexus injury or a cerebrovascular accident. This highlights the need for a comprehensive differential diagnosis in the postoperative period to ensure accurate identification and management of underlying conditions.

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