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用于诊断和治疗局限性朗格汉斯细胞组织细胞增多症(骨嗜酸性肉芽肿)的经皮技术。

Percutaneous techniques for the diagnosis and treatment of localized Langerhans-cell histiocytosis (eosinophilic granuloma of bone).

作者信息

Yasko A W, Fanning C V, Ayala A G, Carrasco C H, Murray J A

机构信息

University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.

出版信息

J Bone Joint Surg Am. 1998 Feb;80(2):219-28. doi: 10.2106/00004623-199802000-00009.

Abstract

We retrospectively studied the outcome of percutaneous needle biopsy and intralesional injection of a corticosteroid (methylprednisolone) in thirty-nine patients who had localized Langerhans-cell histiocytosis (eosinophilic granuloma of bone). All thirty-nine patients had a solitary symptomatic lesion at presentation; a second lesion developed in two patients, two and four months after the first lesion was diagnosed. Therefore, there were forty-one lesions in thirty-nine patients. Fine-needle aspiration with or without core-needle biopsy was performed for all forty-one lesions, and the diagnosis of Langerhans-cell histiocytosis was established for thirty-seven (90 per cent). A corticosteroid was injected into thirty-five lesions. Twenty-nine received the injection at the time of the fine-needle aspiration on the basis of the cytological findings in the aspirate. Six patients who had a solitary lesion had a two-stage procedure because the injection was delayed until the diagnosis was confirmed with histological evaluation of specimens obtained by core-needle biopsy. Thirty-four (97 per cent) of the thirty-five lesions healed. The clinical symptoms associated with thirty-one lesions resolved within two weeks after a single injection of the corticosteroid. There were no complications associated with either the biopsy or the injection. At a median of ninety months (range, twenty-four to 199 months), no patient had recurrence of symptoms or of radiographic evidence of the lesion. All patients who had been managed with an intralesional injection of the corticosteroid had full range of motion of the affected extremity and had resumed unlimited activities. Although the mechanism of action of intralesional injection of a corticosteroid has not been defined, use of percutaneous needle biopsy to diagnose localized Langerhans-cell histiocytosis and treatment with intralesional administration of methylprednisolone relieved pain expeditiously, enabled the patient to avoid an operative procedure, and resulted in osseous healing. The specific role of corticosteroid therapy remains to be determined by prospective, randomized studies.

摘要

我们回顾性研究了39例局限性朗格汉斯细胞组织细胞增多症(骨嗜酸性肉芽肿)患者经皮穿刺针活检及病灶内注射皮质类固醇(甲泼尼龙)的治疗结果。所有39例患者初诊时均有单个有症状的病灶;2例患者在首个病灶确诊后2个月和4个月出现了第二个病灶。因此,39例患者共有41个病灶。对所有41个病灶均进行了细针穿刺抽吸,部分同时进行了粗针活检,其中37个(90%)确诊为朗格汉斯细胞组织细胞增多症。对35个病灶注射了皮质类固醇。29例根据抽吸物的细胞学检查结果在细针穿刺抽吸时即接受了注射。6例有单个病灶的患者采用了两阶段操作,因为注射延迟至通过粗针活检获得的标本经组织学评估确诊后进行。35个病灶中有34个(97%)愈合。单次注射皮质类固醇后,与31个病灶相关的临床症状在两周内消失。活检或注射均未出现并发症。在中位时间90个月(范围24至199个月)时,没有患者出现症状复发或病灶的影像学证据。所有接受病灶内注射皮质类固醇治疗的患者患侧肢体活动范围正常,已恢复无限制活动。尽管病灶内注射皮质类固醇的作用机制尚未明确,但经皮穿刺针活检用于诊断局限性朗格汉斯细胞组织细胞增多症以及病灶内注射甲泼尼龙治疗可迅速缓解疼痛,使患者避免手术,并实现骨质愈合。皮质类固醇治疗的具体作用仍有待前瞻性随机研究确定。

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