首页> 外文期刊>Acta Cytologica: The Journal of Clinical Cytology and Cytopathology >Aspiration cytology of mesenchymal hamartoma of the chest wall in an infant: a case report.
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Aspiration cytology of mesenchymal hamartoma of the chest wall in an infant: a case report.

机译:婴儿胸壁间质错构瘤的抽吸细胞学检查:一例病例报告。

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BACKGROUND: Mesenchymal hamartoma of the chest wall is an extremely uncommon lesion of infants. Radiologic features simulate a malignant neoplasm; however, pathologic examination demonstrates an admixture of fibroblasts, benign cartilage and woven bone. There is a paucity of cytologic reports of this rare entity in the available literature. CASE: A 5-month-old infant presented with a large right chest wall swelling. Radiologic investigation demonstrated lytic destruction of the right 7th, 8th and 9th ribs with a large soft tissue mass. Fine needle aspiration smears showed lobules of hyaline cartilage and a few spindle cells with abundant chondromyxoid matrix. A cytologic diagnosis of a benign chondroid, possibly hamartomatous lesion was given, which was confirmed as mesenchymal hamartoma on histopathologic examination. CONCLUSION: Mesenchymal hamartoma is a rare chest wall lesion that can be diagnosed on cytology, provided that the cytopathologist is aware of this uncommon entity and appreciates the benign cytologic features.
机译:背景:胸壁间质错构瘤是婴儿极为罕见的病变。放射学特征可模拟恶性肿瘤;然而,病理检查显示成纤维细胞,良性软骨和编织骨的混合物。现有文献中很少有这种稀有实体的细胞学报告。病例:一个5个月大的婴儿右胸壁肿大。放射学检查显示右第7,第8和第9肋的溶解性破坏,软组织肿块较大。细针穿刺涂片显示小叶透明软骨和少数纺锤体细胞,具有丰富的软骨粘液基质。进行了良性软骨样病变的细胞学诊断,可能是错构瘤性病变,经组织病理学检查证实为间质错构瘤。结论:间质错构瘤是一种罕见的胸壁病变,可以通过细胞学诊断,只要细胞病理学家意识到这种罕见的现象并欣赏良性细胞学特征即可。

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