Yunce Muharrem, Selinger Stephen, Krimsky William, Harley Daniel P
Department of Internal Medicine, MedStar Franklin Square Medical Center, Baltimore, MD, USA.
Department of Pulmonary and Critical Care Medicine, MedStar Franklin Square Medical Center, Baltimore, MD, USA.
J Community Hosp Intern Med Perspect. 2018 Feb 6;8(1):29-31. doi: 10.1080/20009666.2018.1424485. eCollection 2018.
Primary malignant melanoma of the lung (PMML) is a rare malignancy that exhibits aggressive behavior and has a very poor prognosis. We are reporting on a case of PMML in an otherwise healthy 22-year-old Caucasian male with no significant past medical history and an unremarkable family history. The patient initially presented with a 2-month history of a cough and an unexplained 22-lb weight loss. His initial chest X-ray demonstrated opacification of the right lower lobe (RLL) of his lung and a subsequent computerized tomography scan (CT scan) of his lung revealed a large mass occupying most of his RLL (Figure 1). The patient subsequently underwent a bronchoscopy with endobronchial ultrasound. Biopsies revealed a poorly differentiated carcinoma. A positron emission tomography with low dose CT scan was performed per protocol and revealed an intensely hypermetabolic tumor with no evidence for lymphatic disease or extra-thoracic spread. The patient underwent a surgical exploration and a right lower lobectomy with a thoracic lymphadenectomy. The pathology including immunohistochemical stains demonstrated a malignant melanoma with no lymph node involvement. A physical examination including ophthalmic, mucosal, and skin examinations revealed no evidence for an extra-thoracic site of the disease. The patient had negative margins for resection and did not receive any adjuvant therapy and is alive and well with no evidence for recurrence 3 years after the resection.
原发性肺恶性黑色素瘤(PMML)是一种罕见的恶性肿瘤,具有侵袭性,预后很差。我们报告一例PMML病例,患者为一名22岁健康的白种男性,既往无重大病史,家族史无异常。患者最初出现咳嗽2个月,原因不明地体重减轻22磅。他最初的胸部X线显示右肺下叶(RLL)有致密影,随后的肺部计算机断层扫描(CT扫描)显示一个大肿块占据了大部分RLL(图1)。患者随后接受了支气管镜检查及支气管内超声检查。活检显示为低分化癌。按照方案进行了正电子发射断层扫描及低剂量CT扫描,显示一个代谢极度活跃的肿瘤,无淋巴疾病或胸外扩散的证据。患者接受了手术探查及右下叶切除术和胸段淋巴结清扫术。病理检查包括免疫组化染色显示为恶性黑色素瘤,无淋巴结受累。包括眼科、黏膜和皮肤检查在内的体格检查未发现疾病胸外部位的证据。患者手术切缘阴性,未接受任何辅助治疗,切除术后3年仍存活且状况良好,无复发迹象。