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颅顶淋巴瘤与其他颅骨肿瘤相比的骨质破坏特征

Characteristics of Bone Destruction in Cranial Vault Lymphoma Compared with Other Skull Tumors.

作者信息

Umemura Takeru, Nakano Yoshiteru, Soejima Yoshiteru, Saito Takeshi, Kitagawa Takehiro, Miyaoka Ryo, Suzuki Kohei, Yamamoto Junkoh

机构信息

Department of Neurosurgery, School of Medicine, University of Occupational and Environmental Health, Japan.

出版信息

J UOEH. 2019;41(3):335-342. doi: 10.7888/juoeh.41.335.

Abstract

Cranial vault lymphomas are rare and challenging to diagnose. We present herein two cases of cranial vault lymphoma. The first patient was a 72-year-old woman who presented with a large mass in the parietal bone found incidentally following a head injury. The second patient was a 63-year-old man who presented with an occipital subcutaneous mass associated with visual disturbance and occipital headaches. The diagnosis of a malignant tumor in the second patient was straightforward due to his symptoms and considerable bone destruction, but the first patient was more difficult to diagnose due to a lack of symptoms and only slight bone destruction detected by computed tomography (CT). Both were histophathologically diagnosed with diffuse large B cell lymphoma (DLBCL) in the cranial vault. We also investigated the clinical features, including initial symptoms and patterns of bone destruction, in 23 patients with other types of skull tumors. This comparison showed that cranial vault lymphomas cause large masses on the scalp and lead to characteristic incomplete bone destruction, indicating that cranial bone is destroyed very slowly despite the expanding subcutaneous mass. This feature is unique compared with other benign and malignant skull tumors. In addition, cranial vault lymphoma can be confirmed via bone window CT.

摘要

颅骨淋巴瘤较为罕见,诊断颇具挑战性。我们在此报告两例颅骨淋巴瘤病例。首例患者为一名72岁女性,在头部受伤后偶然发现顶骨有一巨大肿块。第二例患者是一名63岁男性,出现枕部皮下肿块,并伴有视力障碍和枕部头痛。由于第二例患者的症状及明显的骨质破坏,其恶性肿瘤的诊断较为明确,但首例患者因无症状且计算机断层扫描(CT)仅发现轻微骨质破坏,诊断更为困难。两者经组织病理学检查均诊断为颅骨弥漫性大B细胞淋巴瘤(DLBCL)。我们还研究了23例其他类型颅骨肿瘤患者的临床特征,包括初始症状和骨质破坏模式。这种比较表明,颅骨淋巴瘤可导致头皮出现巨大肿块,并导致特征性的不完全骨质破坏,这表明尽管皮下肿块不断增大,但颅骨破坏非常缓慢。与其他良性和恶性颅骨肿瘤相比,这一特征较为独特。此外,颅骨淋巴瘤可通过骨窗CT得以确诊。

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