Chen Li-Qian, Yang Mai-Qing, Gao Su-Mei, Wang Zheng-Jiang, Xu Hong-Tao
Department of Pathology, Weifang People's Hospital (First Affiliated Hospital of Shandong Second Medical University), Weifang, Shandong 261041, P.R. China.
Department of Pathology, The First Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.
Exp Ther Med. 2024 Jul 16;28(3):369. doi: 10.3892/etm.2024.12658. eCollection 2024 Sep.
Papillary adenoma of the lung, a rare and benign tumor, is easily confused with other primary benign or malignant lung tumors and especially with lung adenocarcinoma that has a papillary growth pattern. Enhanced understanding and an accurate diagnosis of papillary adenomas of the lung are crucial for clinical treatment and prognostic assessment. A 61-year-old man who presented with an opportunistic finding in relation to a left lower lobe lung nodule during an examination was admitted to The First Hospital of China Medical University (Shenyang, China) for further treatment. Computed tomography (CT) revealed a well-circumscribed left lower lobe nodule (diameter, ~1 cm), comprising branched papillae with a fibrovascular core and no other structural components. The tumor cells appeared relatively uniform in shape and well arranged with round or oval nuclei. No nucleoli or mitotic figures were observed. Immunohistochemically, the papillary structures of the tumor cells were strongly and diffusely positive for cytokeratin (CK), CK7, Napsin-A and thyroid transcription factor 1. The Ki-67 index was ~1%. A pathological diagnosis of primary papillary adenoma of the lung was made based on these findings. A left lower-lobe wedge resection was performed and the patient's postoperative course was uneventful. Surgical resection is the preferred treatment. Papillary adenoma of the lung is very rare, and its clinical manifestations and CT images are non-specific. It is important to avoid misdiagnosing of papillary adenoma of the lung as another type of lung tumor, especially adenocarcinoma. A clear understanding of the morphological and immunohistochemical features of papillary adenomas is important for the diagnosis of this rare lung tumor.
肺乳头状腺瘤是一种罕见的良性肿瘤,很容易与其他原发性良性或恶性肺肿瘤混淆,尤其是与具有乳头状生长模式的肺腺癌混淆。加强对肺乳头状腺瘤的认识并准确诊断对于临床治疗和预后评估至关重要。一名61岁男性在检查中偶然发现左肺下叶结节,被收治于中国医科大学附属第一医院(中国沈阳)进行进一步治疗。计算机断层扫描(CT)显示左肺下叶有一个边界清晰的结节(直径约1厘米),由带有纤维血管核心的分支乳头组成,无其他结构成分。肿瘤细胞形态相对一致,核呈圆形或椭圆形,排列整齐。未观察到核仁或有丝分裂象。免疫组化显示,肿瘤细胞的乳头状结构对细胞角蛋白(CK)、CK7、Napsin-A和甲状腺转录因子1呈强弥漫性阳性。Ki-67指数约为1%。根据这些发现做出了原发性肺乳头状腺瘤的病理诊断。进行了左肺下叶楔形切除术,患者术后恢复顺利。手术切除是首选治疗方法。肺乳头状腺瘤非常罕见,其临床表现和CT图像无特异性。避免将肺乳头状腺瘤误诊为其他类型的肺肿瘤,尤其是腺癌,这一点很重要。清楚了解肺乳头状腺瘤的形态学和免疫组化特征对于诊断这种罕见的肺肿瘤很重要。