首页> 外文期刊>Indian journal of cancer. >Solitary calvarial metastases: an unusual presentation of thoracic neuroblastoma.
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Solitary calvarial metastases: an unusual presentation of thoracic neuroblastoma.

机译:孤立性颅盖转移瘤:胸神经母细胞瘤的异常表现。

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摘要

A primary thoracic origin occurs only in 20% of neuroblastomas, and their classical presentation is mediastinal or cord compression. Skeletal metastases of neuroblastomas are characteristically multiple, and calvarial deposits usually show simultaneous involvement of orbit. Solitary metastases in neuroblastoma, is an unusual entity and its presentation as a large calvarial mass, especially from a thoracic primary, is rare. Furthermore, calvarial metastases are relatively uncommon in children compared to adults. We discuss the clinical, radiographic, CT features, and differential diagnosis of a large calvarial mass with sunray spiculation in a child, which was due to a solitary metastases from an occult thoracic neuroblastoma. The possibility of neuroblastoma presenting in this unique fashion and the importance of considering a chemosensitive tumor such as neuroblastoma in the differential diagnosis of a solitary calvarial mass in a child is highlighted by our report.
机译:胸源性起源仅发生在20%的神经母细胞瘤中,其经典表现是纵隔或脐带受压。神经母细胞瘤的骨骼转移特征性地是多发的,颅盖沉积物通常显示出眼眶同时受累。神经母细胞瘤中的孤立转移是一个不寻常的现象,其表现为较大的颅盖肿块,尤其是来自胸原发灶的肿块。此外,与成年人相比,颅骨转移在儿童中相对较少见。我们讨论了儿童颅底大块肿物伴有日光针刺的临床,影像学,CT特征和鉴别诊断,这是由于隐匿性胸神经母细胞瘤发生了孤立性转移所致。我们的报告强调了神经母细胞瘤以这种独特方式出现的可能性以及考虑化学敏感性肿瘤(例如神经母细胞瘤)对儿童孤立颅盖肿块的鉴别诊断的重要性。

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