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隐源性机化性肺炎表现为局灶性肺肿块的罕见病例:一例报告及文献复习

Unusual Presentation of Cryptogenic Organising Pneumonia as a Focal Lung Mass: A Case Report and Literature Review.

作者信息

Ng Boon Hau, Low Hsueh Jing, Abeed Nik Nuratiqah Nik, Sharil Nor Safiqah, Osman Rose Azzlinda, Ban Andrea Yu-Lin

机构信息

Respiratory Unit, Department of Medicine, Hospital Canselor Tuanku Muhriz, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia.

Department of Anesthesiology and Critical Care, Hospital Canselor Tuanku Muhriz, Faculty of Medicine Universiti Kebangsaan Malaysia Kuala Lumpur Malaysia.

出版信息

Respirol Case Rep. 2025 Mar 5;13(3):e70138. doi: 10.1002/rcr2.70138. eCollection 2025 Mar.

Abstract

Organising pneumonia (OP) is a distinct pathological pattern characterised by the presence of granulation tissue buds composed of fibroblasts and myofibroblasts embedded in a loose connective tissue matrix within the distal pulmonary airspaces. When OP occurs without an identifiable cause or etiologic context, it is termed cryptogenic organising pneumonia (COP). The diagnosis of OP can be challenging due to its diverse clinical presentations, including the idiopathic form and various secondary forms associated with underlying diseases. We report a case of a middle-aged male presenting with intermittent cough and haemoptysis. Initial sputum analysis was unremarkable, and the patient showed no improvement with antibiotic therapy. Chest radiography showed left lower zone consolidation. Computed tomography (CT) thorax revealed a mass in the left lower lobe, while positron emission tomography-computed tomography (PET/CT) demonstrated a hypermetabolic lesion at the same site. Bronchoscopic bronchoalveolar lavage was negative for tuberculosis, respiratory pathogens, and malignancy. Autoimmune screening yielded negative results. A transthoracic tru-cut lung biopsy confirmed the diagnosis of OP. The patient was treated with prednisolone, leading to significant clinical improvement and complete resolution of the lesion on follow-up CT imaging.

摘要

机化性肺炎(OP)是一种独特的病理模式,其特征是在远端肺气腔内由成纤维细胞和肌成纤维细胞组成的肉芽组织芽嵌入疏松结缔组织基质中。当OP发生时无明确病因或病因背景时,称为隐源性机化性肺炎(COP)。由于OP临床表现多样,包括特发性形式和与基础疾病相关的各种继发性形式,其诊断可能具有挑战性。我们报告一例中年男性,表现为间歇性咳嗽和咯血。初始痰液分析无异常,患者接受抗生素治疗后无改善。胸部X线显示左下肺实变。胸部计算机断层扫描(CT)显示左肺下叶有一肿块,而正电子发射断层扫描-计算机断层扫描(PET/CT)显示同一部位有高代谢病变。支气管镜下支气管肺泡灌洗未发现结核、呼吸道病原体及恶性肿瘤。自身免疫筛查结果为阴性。经胸壁穿刺肺活检确诊为OP。患者接受泼尼松龙治疗,临床症状显著改善,随访CT影像显示病变完全消退。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f3/11880684/e351d22f2ac8/RCR2-13-e70138-g002.jpg

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