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De novo development of intraosseous cavernous hemangioma.

机译:从头发展骨内海绵状血管瘤。

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摘要

Intraosseous cavernous hemangiomas are rare and not often multifocal. De novo development of a skull cavernous hemangioma has not been described previously. We present a 20-year-old man who was operated upon for a skull cavernoma in the right frontal area and developed a new lesion 3 years later in the right occipital region. The first lesion was removed completely and the postoperative course was uneventful. Histology showed an intraosseous cavernous hemangioma. MRI follow-up revealed a new lesion in the right occipital region. At the time of the first operation this lesion was not seen on CT or MRI scan. Surgical removal was performed and histology again showed a cavernous hemangioma. The patient seems to be unique and it is important to keep young patients with the diagnosis of cavernous hemangioma under close follow-up. This supports the experience from parenchymatous cavernous hemangiomas that this malformation may become a dynamic disease.
机译:骨内海绵状血管瘤很少见,而且多灶性。头颅海绵状血管瘤从头发展从未有过描述。我们介绍了一名20岁男子,他在右额叶区域进行了颅骨海绵状瘤的手术,并在3年​​后在右枕骨区域发展了新的病变。完全清除了第一个病变,术后过程平稳。组织学显示骨内海绵状血管瘤。 MRI随访显示右枕骨区域有新病变。在第一次手术时,在CT或MRI扫描中未发现该病变。进行手术切除,组织学再次显示为海绵状血管瘤。该患者似乎是独特的,重要的是要对年轻患者进行海绵状血管瘤的诊断并密切随访。这支持了来自实质性海绵状血管瘤的经验,即这种畸形可能成为动态疾病。

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