From the University of Maryland School of Medicine, Baltimore, MD.
University of Chicago Pritzker School of Medicine, Chicago, IL.
J Comput Assist Tomogr. 2024;48(1):98-103. doi: 10.1097/RCT.0000000000001536. Epub 2023 Aug 7.
The purpose of this study is to bring attention to an atypical form of metastatic pulmonary calcification, which is conventionally described as a metabolic process with upper lobe predominance in patients with a specific clinical history, which has not been reported as a distinct entity.
Patients with metastatic pulmonary calcification (MPC) were first identified with mPower keyword search, including MPC or metastatic calcifications on computed tomography chest radiological reports. Patients were then filtered on likelihood of MPC based off imaging reports. Images were then reviewed by three senior radiologists for pertinent characteristics such as location of MPC, degree of calcifications and pleural effusions. Based on the predominant location of MPC, cases were labeled as either typical or atypical. Clinical and imaging characteristics relevant to MPC were noted and compared across typical and atypical cases.
In our study, we describe 25 patients with MPC, 13 defined as typical MPC and 12 with atypical MPC. Through consensus of senior radiologists, MPC was deemed to be mild (52%), moderate (44%), or severe (4%). Twenty-three patients (92%) had underlying renal disease including 21 requiring dialysis at the time of diagnosis. Outside of age at diagnosis, there was no significant clinical difference between the two groups. Evaluation of imaging characteristics (average HU attenuation, 267; range, 186-295), pattern and distribution of calcification, and clinical history strongly supported a diagnosis of atypical MPC.
This study presents several cases of lower lobe subpleural MPC associated with pleural effusions, which has not been reported as a distinct entity, despite comprising a significant portion of MPC cases at our institution.
本研究旨在引起人们对一种非典型形式的转移性肺钙化的关注,这种钙化通常被描述为一种代谢过程,在上肺叶中占优势,且发生于具有特定临床病史的患者中,但尚未被报道为一种独特的实体。
首先通过 mPower 关键字搜索确定转移性肺钙化(MPC)患者,包括胸部 CT 放射学报告中的 MPC 或转移性钙化。然后根据影像学报告对 MPC 的可能性进行过滤。然后由三位资深放射科医生对图像进行审查,以确定 MPC 的位置、钙化程度和胸腔积液等相关特征。根据 MPC 的主要位置,将病例标记为典型或非典型。记录与 MPC 相关的临床和影像学特征,并对典型和非典型病例进行比较。
在我们的研究中,我们描述了 25 例 MPC 患者,其中 13 例被定义为典型 MPC,12 例为非典型 MPC。通过资深放射科医生的共识,MPC 被认为是轻度(52%)、中度(44%)或重度(4%)。23 例(92%)患者存在基础肾脏疾病,包括 21 例在诊断时需要透析。除了诊断时的年龄外,两组之间没有明显的临床差异。对影像学特征(平均 HU 衰减值,267;范围,186-295)、钙化的模式和分布以及临床病史的评估强烈支持非典型 MPC 的诊断。
本研究提出了几例与胸腔积液相关的下叶胸膜下 MPC 的病例,尽管在我们机构中占 MPC 病例的很大一部分,但尚未被报道为一种独特的实体。