Takizawa Yuko, Taniuchi Namiko, Ghazizadeh Mohammad, Enomoto Tatsuji, Sato Masashi, Jin Enjing, Azuma Arata, Gemma Akihiko, Kudoh Shoji, Kawanami Oichi
Department of Molecular Pathology, Graduate School of Medicine, Nippon Medical School, Kawasaki, Kanagawa, Japan.
J Nippon Med Sch. 2009 Apr;76(2):84-92. doi: 10.1272/jnms.76.84.
Histiocytes of Langerhans cell type are recovered from the bronchoalveolar lavage fluid (BALF) of patients with interstitial lung diseases in a nonspecific manner. Langerhans cells (LCs) can be identified through immunostaining for S-100, CD1a, and, more specifically, langerin. To evaluate the diagnostic value of BALF in pulmonary Langerhans cell histiocytosis (PLCH), we performed a retrospective clinicopathological study of 5 patients with biopsy-confirmed PLCH or Hand-Schüller-Christian disease involving the lung. As a control study, we examined BALF cells from 23 patients with various diseases, including sarcoidosis, hypersensitivity pneumonitis, collagen vascular disease, idiopathic pulmonary fibrosis, and adenocarcinoma of the lung. Cytospins obtained from BALF were stained with Giemsa or Papanicoloau and others were immunostained. In general, cytospins showed a monomorphous and dispersed cell population containing mononucleated or binucleated and occasionally multinucleated histiocytes. LCs recovered from BALF were characterized by clear and velvety cytoplasm; oval or kidney-shaped, vesicular nuclei with irregular shapes; nucleoli; and frequent grooves and indentations. Radiography and high-resolution computed tomography showed multiple bilateral nodular or cystic lesions in the middle and upper lung zones. The mean percentage of LCs in 9 lavages from the 5 patients was 8.0%, whereas that from the control group was only 0.3% (maximum, 1.6%). The percentage of cells positive for S-100 or CD1a was comparable to the percentage of Langerhans-like histiocytes stained with Giemsa stain. The present results indicate that the survey of LCs in BALF with the aid of immunocytochemical evaluation and corresponding clinical data could play a critical role in establishing the diagnosis of PLCH, thus providing a less invasive approach than lung biopsy, which carries a risk of complications.
在间质性肺疾病患者的支气管肺泡灌洗(BALF)中可非特异性地发现朗格汉斯细胞型组织细胞。朗格汉斯细胞(LCs)可通过S-100、CD1a免疫染色,更确切地说是通过朗格素免疫染色来识别。为评估BALF在肺朗格汉斯细胞组织细胞增多症(PLCH)中的诊断价值,我们对5例经活检确诊为PLCH或累及肺部的汉-许-克病患者进行了回顾性临床病理研究。作为对照研究,我们检查了23例患有各种疾病患者的BALF细胞,这些疾病包括结节病、过敏性肺炎、胶原血管病、特发性肺纤维化和肺腺癌。从BALF获得的细胞涂片用吉姆萨或巴氏染色,其他涂片进行免疫染色。一般来说,细胞涂片显示为单一形态且分散的细胞群,包含单核或双核,偶尔还有多核组织细胞。从BALF中回收的LCs的特征为细胞质清晰且呈天鹅绒样;椭圆形或肾形、形状不规则的泡状核;核仁;以及频繁的沟和凹陷。放射学检查和高分辨率计算机断层扫描显示中、上肺区有多个双侧结节状或囊性病变。5例患者的9次灌洗中LCs的平均百分比为8.0%,而对照组仅为0.3%(最高为1.6%)。S-100或CD1a阳性细胞的百分比与吉姆萨染色的朗格汉斯样组织细胞的百分比相当。目前的结果表明,借助免疫细胞化学评估和相应临床数据对BALF中的LCs进行检测在PLCH诊断中可能起关键作用,从而提供一种比肺活检侵入性更小的方法,肺活检存在并发症风险。