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C1-C2色素沉着绒毛结节性滑膜炎与透明细胞癌:一种罕见疾病的意外表现及文献综述

C1-C2 pigmented villonodular synovitis and clear cell carcinoma: unexpected presentation of a rare disease and a review of the literature.

作者信息

Lavrador José Pedro, Oliveira Edson, Gil Nuno, Francisco António Fernandes, Livraghi Sérgio

机构信息

Neurosurgical Department, Hospital Santa Maria, Lisbon, Portugal,

出版信息

Eur Spine J. 2015 May;24 Suppl 4:S465-71. doi: 10.1007/s00586-014-3396-6. Epub 2014 Jun 8.

DOI:10.1007/s00586-014-3396-6
PMID:24908254
Abstract

INTRODUCTION

Pigmented Villonodular synovitis (PVNS) is a rare vertebral pathology--around 50 reports, only 3 concerning C1-C2 location.

CASE REPORT

A 64-year-old man, submitted to a right nephrectomy for a clear cell carcinoma, presented with an asymptomatic osteolytic C1-C2 lesion. Even though the diagnosis of metastatic disease was the most probable, the presence of a solitary lesion without other osseous or systemic localization and the predicted low risk of recurrence imposed a surgical biopsy. A pigmented villonodular synovitis diagnosis was made, a rare vertebral pathology--around 50 reports, only 3 concerning C1-C2 location. No further treatment was assigned precluding the iatrogenic consequences of empirical treatments based on clinical diagnosis with no histopathological support. The patient remains stable at 18 months of follow-up.

CONCLUSION

A large differential diagnosis should be made when the typical findings for metastatic disease are absent precluding the iatrogenic consequences of empirical treatments based on clinical diagnosis with no histopathological support.

摘要

引言

色素沉着绒毛结节性滑膜炎(PVNS)是一种罕见的脊柱病变——约有50例报告,仅3例涉及C1-C2节段。

病例报告

一名64岁男性,因透明细胞癌接受了右肾切除术,出现了一个无症状的C1-C2溶骨性病变。尽管转移性疾病的诊断可能性最大,但存在孤立性病变且无其他骨或全身定位,以及预测的低复发风险,因此进行了手术活检。诊断为色素沉着绒毛结节性滑膜炎,这是一种罕见的脊柱病变——约有50例报告,仅3例涉及C1-C2节段。未给予进一步治疗,以避免基于无组织病理学支持的临床诊断进行经验性治疗所带来的医源性后果。患者在随访18个月时保持稳定。

结论

当缺乏转移性疾病的典型表现时,应进行广泛的鉴别诊断,以避免基于无组织病理学支持的临床诊断进行经验性治疗所带来的医源性后果。

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