[Pheochromocytoma: role of preoperative diagnosis in the assessment of malignancy risk and in the choice of surgical approach].

C P Lombardi, M Raffaelli, C De Crea, E Traini, A M D'Amore, R Bellantone
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Abstract

Pheochromocytomas are malignant in 5-26% of the cases. Differential diagnosis with benign lesions can be difficult even on a pathological basis. Local invasion and distant metastasis are the only well established indicators of malignancy. It has been reported that the risk of malignancy increases with the lesion size. Despite safe laparoscopic adrenalectomy (LA) has been reported for lesions up to 10 cm, it is considered hazardous for pheochromocytoma larger than 6 cm, because of the risk of malignancy and iatrogenic pheochromocytomatosis. We evaluated the possibility to pre-operatively recognize pheochromocytomas at risk of being malignant that should not be selected for LA. The medical records of all the patients who underwent adrenalectomy for pheochromocytoma were reviewed. All the preoperatively available data (demographic, clinical, biochemical and radiological) were recorded as well as final pathological diagnosis. Comparative analysis of patients with benign and malignant pheochromocytomas was performed. Sixty-three adrenalectomies for pheochromocytoma were performed in 60 patients. Fifty-seven benign and 6 malignant pheochromocytomas were identified. No significant difference was found between patients with malignant and benign lesions concerning age, gender, family history, symptoms, laboratory and radiological findings. In particular, no significant difference was found for lesion size between the benign (63.3 +/- 30.6 mm, range, 20-150) and the malignant group (48.6 +/- 16.5 mm; range, 30-70). The largest diameter recorded for a malignant lesion was 70 mm. No preoperatively available data can reliably differentiate between benign and malignant pheochromocytomas. All malignant lesions in this series were smaller than 7 cm. Thus, pheochromocytoma size does not seem a reliable predictor of malignancy. In absence of the evidence of gross local invasion or metastatic disease, LA can be safely proposed also for large lesions. Conversion is mandatory in presence of local invasion or difficult dissection that could involve inadequate resection.

嗜铬细胞瘤:术前诊断在恶性肿瘤风险评估和手术入路选择中的作用。
5-26%的嗜铬细胞瘤为恶性。即使在病理基础上,良性病变的鉴别诊断也是困难的。局部侵袭和远处转移是恶性肿瘤唯一确定的指标。据报道,恶性肿瘤的风险随着病变的大小而增加。尽管安全的腹腔镜肾上腺切除术(LA)已报道病变达10厘米,但由于恶性肿瘤和医源性嗜铬细胞病的风险,对于大于6厘米的嗜铬细胞瘤,它被认为是危险的。我们评估了术前识别有恶性危险的嗜铬细胞瘤的可能性,这些嗜铬细胞瘤不应该被选为LA。本文回顾了所有因嗜铬细胞瘤而行肾上腺切除术的患者的医疗记录。记录所有术前资料(人口学、临床、生化、放射学)及最终病理诊断。对良恶性嗜铬细胞瘤患者进行对比分析。60例肾上腺嗜铬细胞瘤患者行肾上腺切除术63例。良性嗜铬细胞瘤57例,恶性嗜铬细胞瘤6例。恶性病变与良性病变患者在年龄、性别、家族史、症状、实验室及影像学检查等方面无显著差异。特别是,良性组(63.3 +/- 30.6 mm,范围20-150)与恶性组(48.6 +/- 16.5 mm;范围内,30 - 70)。恶性病变记录的最大直径为70毫米。没有术前可用的数据可以可靠地区分良性和恶性嗜铬细胞瘤。所有恶性病变均小于7cm。因此,嗜铬细胞瘤的大小似乎不是恶性肿瘤的可靠预测因子。在没有明显的局部侵犯或转移性疾病证据的情况下,对于较大的病变,也可以安全地推荐LA。如果存在局部侵犯或切除不充分导致解剖困难,则必须进行手术。
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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