一例罕见的无症状巨大肺火腿肠瘤。

IF 2.4 3区 医学 Q2 PATHOLOGY
Xiaoming Fan, Barry Breaux, Laura Leonards, Rusella Mirza
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引用次数: 0

摘要

背景:肺火腿肠瘤是肺部良性病变。从组织病理学角度看,肺火腿肠瘤由不同数量的间质成分组成,包括软骨组织、成熟脂肪组织、纤维基质、平滑肌和夹杂的呼吸道上皮。大多数肺火腿肠瘤病例没有症状,是在影像学检查中偶然发现的。它们通常表现为圆形病变,最大尺寸小于 4 厘米。超过 8 厘米的无症状巨大肺火腿肠瘤非常罕见:在本病例报告中,一名 59 岁的女性在接受心脏病检查时意外发现了一个 12.0 × 9.5 × 7.5 厘米的肺部肿块。大体上,病变呈分叶状,切面呈珍珠白至棕白色实性,并有小囊性区域。显微镜下,具有代表性的肿瘤切片显示为软骨瘤样外观,基质细胞相对较少,外围夹有呼吸道上皮。未发现明显的不典型性。未发现有丝分裂,增殖指数很低(结论:巨大肺火腿肠瘤非常罕见;我们的病例是无症状患者患巨大火腿肠瘤的一个实例。肿瘤的大小令人担忧。因此,需要对病变进行仔细、全面的检查,以做出正确诊断并排除并存的恶性肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of asymptomatic giant pulmonary hamartoma.

Background: Pulmonary hamartomas are benign lung lesions. Histopathologically, pulmonary hamartoma is composed of varying amounts of mesenchymal elements, including chondroid tissue, mature adipose tissue, fibrous stroma, smooth muscle, and entrapped respiratory epithelium. Most pulmonary hamartoma cases are asymptomatic and found incidentally during imaging. They usually appear as well-circumscribed lesions with the largest dimension of less than 4 cm. Asymptomatic giant pulmonary hamartomas that more than 8 cm are rare.

Case presentation: In the current case report, a 12.0 × 9.5 × 7.5 cm lung mass was incidentally noticed in a 59-year-old female during a heart disease workup. Grossly, the lesion was lobulated with pearly white to tan-white solid cut surface and small cystic areas. Microscopically, representative tumor sections demonstrate a chondromyxoid appearance with relatively hypocellular stroma and entrapped respiratory epithelium at the periphery. No significant atypia is noted. No mitosis is noted, and the proliferative index is very low (< 1%) per Ki-67 immunohistochemistry. Mature adipose tissue is easily identifiable in many areas. Histomorphology is consistent with pulmonary hamartoma. A sarcoma-targeted gene fusion panel was further applied to this case. Combined evaluation of microscopic examination and sarcoma-targeted gene fusion panel results excluded malignant sarcomatous transformation in this case. The mediastinal and hilar lymph nodes are histologically benign. After surgery, the patient had an uneventful postoperative period.

Conclusions: Giant pulmonary hamartoma is rare; our case is an example of a huge hamartoma in an asymptomatic patient. The size of this tumor is concerning. Thus, careful and comprehensive examination of the lesion is required for the correct diagnosis and to rule out co-existent malignancy.

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来源期刊
Diagnostic Pathology
Diagnostic Pathology 医学-病理学
CiteScore
4.60
自引率
0.00%
发文量
93
审稿时长
1 months
期刊介绍: Diagnostic Pathology is an open access, peer-reviewed, online journal that considers research in surgical and clinical pathology, immunology, and biology, with a special focus on cutting-edge approaches in diagnostic pathology and tissue-based therapy. The journal covers all aspects of surgical pathology, including classic diagnostic pathology, prognosis-related diagnosis (tumor stages, prognosis markers, such as MIB-percentage, hormone receptors, etc.), and therapy-related findings. The journal also focuses on the technological aspects of pathology, including molecular biology techniques, morphometry aspects (stereology, DNA analysis, syntactic structure analysis), communication aspects (telecommunication, virtual microscopy, virtual pathology institutions, etc.), and electronic education and quality assurance (for example interactive publication, on-line references with automated updating, etc.).
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