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颈髓外淋巴组织细胞样肉芽肿病。

Cervical extramedullary lymphomatoid granulomatosis.

机构信息

Institute of Neurosurgery, Catholic University, Rome 00168, Italy.

出版信息

J Clin Neurosci. 2011 Jun;18(6):851-3. doi: 10.1016/j.jocn.2010.08.042. Epub 2011 Apr 13.

Abstract

Lymphomatoid granulomatosis (LYG) is a rare multisystem disease involving most frequently the lung, kidney and skin. LYG is characterized by an infiltration of atypical lymphocytoid and plasmocytoid cells, with granulomatous inflammation in an angiocentric and angiodestructive pattern. There have been only a few reports of spinal involvement of LYG. To our knowledge, we report the first patient with cervical extramedullary LYG undergoing surgical removal of a lesion causing spinal cord compression, and review the pertinent literature. The patient underwent C5-partial T1 laminectomy with partial removal of the lesion and decompression of the spinal cord. A diagnosis of a grade III LYG was made and chemotherapy with cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP) was administered. The patient was in good neurological condition at the 6-month follow-up but died 5 months later because of systemic progression of the disease. Although prognosis of LYG remains poor, surgery can be considered to improve pain relief and neurological morbidity of spinal LYG.

摘要

淋巴样肉芽肿病(LYG)是一种罕见的多系统疾病,最常累及肺、肾和皮肤。LYG 的特征是浸润性的非典型淋巴样和浆细胞样细胞,并伴有血管中心性和血管破坏性的肉芽肿性炎症。仅有少数 LYG 脊柱受累的报道。据我们所知,我们报告了首例颈椎髓外 LYG 患者,该患者因脊髓压迫而行病变切除手术,并复习相关文献。患者行 C5 部分 T1 椎板切除术,部分切除病变并脊髓减压。诊断为 3 级 LYG,给予环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)化疗。患者在 6 个月的随访时神经状况良好,但 5 个月后因疾病全身进展而死亡。虽然 LYG 的预后仍然较差,但手术可考虑用于改善脊柱 LYG 的疼痛缓解和神经发病率。

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