JinFeng Chen , Min Ao , WeiYi Li , Xian Li , Li Yang
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引用次数: 0
摘要
原发性肺恶性黑色素瘤(Primary malignant melanoma of lung, PMML)相对罕见,约占所有恶性黑色素瘤的0.4%,仅占所有肺肿瘤的0.01%,诊断时发现远处转移的PMML极为罕见。本研究报告1例PMML表现为多发性实性及磨玻璃性肺结节,伴脑、肝、肺内及淋巴结转移。患者42岁,男,在我院神经内科对症治疗后头痛10天,上述症状未见改善。头颅MRI认为多发结节。胸部CT示右肺上下叶2个实性结节,双肺多发磨玻璃结节。为进一步明确诊断,行ct引导下经皮肺结节穿刺活检。病理示肺恶性黑色素瘤。NRAS + BRAF基因检测显示BRAF基因外显子15 V600E突变,出院后给予达拉非尼、曲美替尼靶向治疗。随访1个月后,所有病变均明显减少。PMML表现为实性和磨砂玻璃肺结节并多发性转移是极为罕见的。病理活检和基因检测的早期识别对于精确治疗和提高预后至关重要。
Primary pulmonary malignant melanoma with multiple metastases: a case report and literature review
Primary malignant melanoma of lung (PMML) are relatively rare, accounting for about 0.4 % of all malignant melanomas and only 0.01 % of all lung tumors, and PMML with distant metastases found at diagnosis is extremely rare. A case of PMML presented as multiple solid and ground glass pulmonary nodules with brain, liver,intrapulmonary and lymph nodes metastasis was reported in this study. A 42-year-old man had a headache for 10 days after symptomatic treatment in the department of neurology in our hospital, but the above symptoms did not improved. Multiple nodules were considered by head MRI. Chest CT showed two solid nodules in the upper and lower lobes of the right lung and multiple ground glass nodules in both lungs. To further clarify the diagnosis,CT-guided percutaneous puncture biopsy of pulmonary nodule was performed. The pathology revealed malignant melanoma of <lung>.NRAS + BRAF gene test, showing BRAF gene exon 15 V600E mutation Dalafenib and trametinib were given targeted therapy after discharge. After 1 month follow-up, all lesions were significantly decreased. PMML presenting as solid and ground glass pulmonary nodules with multiple metastases is extremely rare. The early identification of pathological biopsy and genetic testing is crucial for precise treatment and enhancing prognosis.