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支气管肺泡灌洗细胞表面CD1表达对诊断组织细胞增多症X的价值——我们的经验

[Usefulness of CD1 expression on surfaces of cells in bronchoalveolar fluid for diagnosis of histiocytosis X--our experience].

作者信息

Sledziewska J, Rogińska E, Obłakowski P, Słodkowska J, Hawryłkiewicz I, Kuś J, Pawlicka L, Pirozyński M, Rowińska-Zakrzewska E

机构信息

III Kliniki Gruźlicy i Chorób Płuc, Warszawie.

出版信息

Pneumonol Alergol Pol. 1999;67(7-8):311-7.

Abstract

Histiocytosis X (HX), also referred as Langerhans cell granulomatosis is a disorder characterized by the presence of destructive granulomas containing Langerhans cells, lymphocytes, eosinophils and fibroblastes in the involved organs. Three presentations are commonly observed: 1) nonproductive cough or effort dyspnea, 2) spontaneous pneumothorax 3) incidental pulmonary infiltrates on chest X-ray in asymptomatic patients. HRCT may be helpful in the initial diagnosis of pulmonary HX. HRCT scans show nodules, cysts and estimate the extent of disease. But the final diagnosis of histiocytosis X requires the histologic demonstration of specific histiocytosis X cell in biopsy specimens of the lung. The aim of this study was to define the importance of the detection of Langerhans cells in bronchoalveolar lavage fluid (BALF) for the diagnosis of HX. The searched cells express a specific CD1 antigen, recognized by the monoclonal antibody OKT-6. In our study the demonstration of more than 5% of CD1 positive cells was defined to confirm HX. We have studied the BALF in 21 patients with suspected histiocytosis X. In BALF of 4 patients more than 5% of CD1 positive cells were found. In 1 of them HX was confirmed with open lung biopsy. Two patients displayed 5% of CD1 positive cells. The final diagnosis of the first patient was hypersensitivity pneumonitis and of the second one was bronchitis chronica. In 5 patients out of 15 patients in whom less than 5% of CD1 positive cells were found histiocytosis X was histologically proven. In other 10 patients the following disorders were histologically recognised: pulmonary emphysema 3 cases, pneumoconiosis-3, LMA-BOOP-1, sarcoidosis-1 and pleuritis eosinophilica-1. The estimation of Langerhans cells in BALF can be a useful method among the diagnostic procedures for histiocytosis X. It is necessary to remember that demonstration of less than 5% of CD1 positive cells do not exclude histiocytosis X.

摘要

组织细胞增多症X(HX),也称为朗格汉斯细胞组织细胞增生症,是一种以受累器官中存在含有朗格汉斯细胞、淋巴细胞、嗜酸性粒细胞和成纤维细胞的破坏性肉芽肿为特征的疾病。通常观察到三种表现:1)干咳或劳力性呼吸困难,2)自发性气胸,3)无症状患者胸部X线检查时偶然发现的肺部浸润。高分辨率计算机断层扫描(HRCT)可能有助于肺部HX的初步诊断。HRCT扫描可显示结节、囊肿并评估疾病范围。但组织细胞增多症X的最终诊断需要在肺活检标本中进行特定组织细胞增多症X细胞的组织学证明。本研究的目的是确定在支气管肺泡灌洗(BALF)液中检测朗格汉斯细胞对HX诊断的重要性。所检测的细胞表达一种特定的CD1抗原,可被单克隆抗体OKT-6识别。在我们的研究中,定义为超过5%的CD1阳性细胞可确诊HX。我们研究了21例疑似组织细胞增多症X患者的BALF。在4例患者的BALF中发现超过5%的CD1阳性细胞。其中1例经开胸肺活检确诊为HX。2例患者显示5%的CD1阳性细胞。第一例患者的最终诊断为过敏性肺炎,第二例为慢性支气管炎。在15例发现少于5%的CD1阳性细胞的患者中,5例经组织学证实为组织细胞增多症X。在其他10例患者中,经组织学诊断为以下疾病:肺气肿3例、尘肺3例、淋巴细胞性间质性肺炎-细支气管炎伴机化性肺炎(LMA-BOOP)1例、结节病1例和嗜酸性粒细胞性胸膜炎1例。在组织细胞增多症X的诊断程序中,BALF中朗格汉斯细胞的评估可能是一种有用的方法。必须记住,少于5%的CD1阳性细胞的证明并不排除组织细胞增多症X。

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