Minami Yuko, Iijima Tatsuo, Yamamoto Tatsuo, Morishita Yukio, Terashima Hideo, Onizuka Masataka, Noguchi Masayuki
Department of Surgery, Institute of Clinical Medicine, University of Tsukuba, Ibaraki, Japan.
Pathol Res Pract. 2005;200(11-12):813-6. doi: 10.1016/j.prp.2004.09.009.
Pulmonary hamartoma usually occurs as a benign, well-circumscribed single nodule in the lung parenchyma. We report on a unique case of hamartoma that extended along the bronchial tree, formed endobronchial polypoid lesions, and expanded into the lung parenchyma. The patient, a 48-year-old man, was admitted with dyspnea and chest pain. A transbronchial biopsy was performed on a tumorous lesion that was diagnosed histologically as a hamartoma. As this lesion was found to be growing diffusely along the bronchial tree, a left pneumonectomy was performed. Gross examination showed that yellowish soft tissue had surrounded the bronchial tree and extended into the lung parenchyma. Histologically, the lesion contained mainly mature adipose tissue, cartilage, and muscle tissue with a minor component of short spindle cells in a myxomatous matrix. The patient was diagnosed as having diffuse pulmonary hamartoma.
肺错构瘤通常表现为肺实质内一个良性、边界清晰的单个结节。我们报告了一例独特的错构瘤病例,该错构瘤沿支气管树生长,形成支气管内息肉样病变,并扩展至肺实质。患者为一名48岁男性,因呼吸困难和胸痛入院。对一个肿瘤性病变进行了经支气管活检,组织学诊断为错构瘤。由于发现该病变沿支气管树弥漫性生长,遂行左肺切除术。大体检查显示,淡黄色软组织围绕支气管树并延伸至肺实质。组织学检查发现,病变主要包含成熟的脂肪组织、软骨和肌肉组织,在黏液样基质中有少量短梭形细胞成分。该患者被诊断为弥漫性肺错构瘤。