Tang Xiaoping, Wu Zihan, Shen Yihong
Department of Respiratory Medicine, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China.
Department of Pathology, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China.
Oncol Lett. 2015 Jul;10(1):250-254. doi: 10.3892/ol.2015.3225. Epub 2015 May 19.
Alveolar adenoma is an extremely rare benign tumor of the lung derived from type II pneumocytes. To date, only a limited number of alveolar adenoma cases have been reported in the literature. These tumors are usually discovered incidentally on radiographic images. However, other tumor types must be excluded when the characteristics of alveolar adenoma are not typical on the radiographic images. Therefore, diagnosis of alveolar adenomas is based on the combination of gross structural analysis and immunohistochemistry. The present study described a case of alveolar adenoma in a 47-year-old female patient. A chest X-ray revealed a pulmonary lesion in the right lower lobe and, subsequently, the patient underwent a right lower lobectomy. Pathological examination of the surgically resected tissue confirmed the initial diagnosis of alveolar adenoma. In addition, intracranial vascular malformations were detected on a computed tomography scan, but the patient did not experience any notable symptoms. Considering the benign nature of the malformations, as determined by digital subtraction angiography, the patient selected to undergo follow-up with observation only. The postoperative course was uneventful and no recurrence of pulmonary lesions was noted after >4 years, while the condition of the intracranial lesion was stable. In conclusion, the current study described a unique case of adenoma alveolar coexisting with intracranial vascular malformations. A literature review of previously-reported alveolar adenoma cases was also conducted.
肺泡腺瘤是一种极为罕见的起源于Ⅱ型肺上皮细胞的肺良性肿瘤。迄今为止,文献中仅报道了有限数量的肺泡腺瘤病例。这些肿瘤通常在影像学检查中偶然发现。然而,当肺泡腺瘤在影像学上的特征不典型时,必须排除其他肿瘤类型。因此,肺泡腺瘤的诊断基于大体结构分析和免疫组织化学的结合。本研究描述了一例47岁女性肺泡腺瘤患者。胸部X线检查发现右下肺有一个肺部病变,随后患者接受了右下肺叶切除术。对手术切除组织的病理检查证实了最初肺泡腺瘤的诊断。此外,计算机断层扫描检测到颅内血管畸形,但患者没有出现任何明显症状。考虑到数字减影血管造影确定的畸形的良性性质,患者选择仅接受观察随访。术后过程顺利,4年多后未发现肺部病变复发,而颅内病变情况稳定。总之,本研究描述了一例肺泡腺瘤与颅内血管畸形共存的独特病例。还对先前报道的肺泡腺瘤病例进行了文献综述。