从诊断活检到大泡切除术:肺朗格汉斯细胞组织细胞增多症的进行性并发症1例

IF 0.7 Q4 RESPIRATORY SYSTEM
Yuan-Chia Hsin , Yung-Chia Huang , Yen-Lin Wu , Shih-Wei Lee , Po-Chun Lo
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引用次数: 0

摘要

一位38岁男性吸烟者表现为持续干咳数周。胸片显示双侧网状结节性混浊主要位于肺上野。随后的胸部计算机断层扫描显示弥漫性、厚壁、不规则囊性病变,主要累及肺中上区,呈小叶中心分布。通过视频胸腔镜手术获得的组织病理学检查显示,细支气管中心结节和囊肿含有朗格汉斯细胞,细胞核卷曲,CD1a、S-100和朗格汉斯细胞免疫组化染色阳性。这些结果证实了肺朗格汉斯细胞组织细胞增多症(PLCH)的诊断。患者戒烟后症状最初有所改善,但并发复发性气胸和大泡形成,最终需要手术干预。本病例强调了PLCH与吸烟之间的关系,强调了手术活检后的潜在并发症,并强调戒烟是一种关键的治疗措施,针对难治性或突变特异性病例保留靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From diagnostic biopsy to bullectomy: A case of progressive complications in pulmonary langerhans cell histiocytosis
A 38-year-old male smoker presented with a persistent dry cough lasting several weeks. Chest radiography showed bilateral reticulonodular opacities predominantly in the upper lung fields. Subsequent chest computed tomography revealed diffuse, thick-walled, irregular cystic lesions mainly involving the mid and upper lung zones with a centrilobular distribution. Histopathological examination obtained through video-assisted thoracoscopic surgery demonstrated bronchiolocentric nodules and cysts containing Langerhans cells with convoluted nuclei, confirmed by positive immunohistochemical staining for CD1a, S-100, and Langerin. These findings confirmed the diagnosis of pulmonary Langerhans Cell Histiocytosis (PLCH). The patient's symptoms improved initially following smoking cessation but were complicated by recurrent pneumothorax and the formation of giant bullae, ultimately requiring surgical intervention. This case emphasizes the association between PLCH and smoking, highlights potential complications following surgical biopsy, and underscores smoking cessation as a critical therapeutic measure, with targeted therapies reserved for refractory or mutation-specific cases.
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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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