Department of Cardiothoracic Surgery, Royal Infirmary of Edinburgh, Edinburgh, Edinburgh, UK
Department of Pathology, Western General Hospital, Edinburgh, UK.
BMJ Case Rep. 2022 Jul 13;15(7):e250249. doi: 10.1136/bcr-2022-250249.
A female patient presented with fever of unknown origin, night sweats and weight loss. She had no pulmonary symptoms. Investigations revealed bilateral ground glass lung lesions which were subsequently followed-up with imaging. Two years later, a follow-up CT scan revealed an increase in the size of the lesions which exhibited a more solid appearance. A diagnostic biopsy was difficult to perform, and the patient underwent a left upper lobectomy for suspected primary lung malignancy. Histological examination showed lung involvement by Castleman's disease of plasma cell type which displayed a multifocal distribution. There was no evidence of nodal involvement. Following discussion at the multidisciplinary team meeting and correlation with radiology, a diagnosis of multicentric Castleman's disease of the lung was made. Here, we present an unusual case of multicentric Castleman's disease of the lung mimicking primary lung carcinoma. Our case highlights the importance of considering this entity in the differential diagnosis of multifocal lung lesions with a ground glass-like appearance to allow early diagnosis and management.
一位女性患者以不明原因发热、盗汗和体重减轻就诊。她没有肺部症状。检查显示双侧磨玻璃样肺病变,随后进行影像学随访。两年后,随访 CT 扫描显示病变大小增加,表现出更坚实的外观。进行诊断性活检很困难,因此患者因疑似原发性肺癌行左肺上叶切除术。组织学检查显示肺实质受累为浆细胞型 Castleman 病,呈多灶性分布。无淋巴结受累证据。在多学科团队会议上进行讨论并与放射学相关联后,诊断为肺多中心 Castleman 病。在此,我们提出了一个不常见的肺多中心 Castleman 病病例,类似于原发性肺癌。我们的病例强调了在具有磨玻璃样外观的多灶性肺部病变的鉴别诊断中考虑这种疾病的重要性,以便早期诊断和治疗。