Key result
Pulmonary artery intimal sarcoma is a rare malignancy mimicking pulmonary embolism, with clinical clues including disproportionately low d-dimer and characteristic CT findings like the 'wall eclipsing sign'.
Why the study?
Pulmonary artery intimal sarcoma is a rare malignancy that closely mimics pulmonary thromboembolism, making prompt recognition of distinguishing clinical and radiological characteristics critical to guide surgical management.
Case Report (n=2)
No
Recognizing specific clinical and radiological signs of pulmonary artery intimal sarcoma can prevent inappropriate anticoagulation and facilitate early surgical management.
May prompt PAIS consideration in atypical PE cases with low biomarkers or wall-eclipsing CTPA signs; leaves open prospective validation.
Pulmonary artery intimal sarcoma (PAIS) is a rare malignancy which closely mimics acute or chronic pulmonary thromboembolism. There are clinical and radiological characteristics which may raise suspicion of this important differential diagnosis. These include disproportionately low d-dimer, troponin T or NT-proBNP, as well as characteristic findings on CT pulmonary angiography such as the 'wall eclipsing sign' and an non-dependent position of filling defects in the large arteries. Prompt diagnosis avoids inappropriate anticoagulation and facilitates early surgical management which may improve prognosis. There is emerging evidence of an effective treatment paradigm with surgical resection and adjuvant chemotherapy. We present two cases of PAIS diagnosed at a single centre within a 2-year period. We review the literature and demonstrate the features at presentation in our cases which were suggestive of the diagnosis.
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Tuft et al. (2022) conducted a case report in Pulmonary artery intimal sarcoma (PAIS) (n=2). Pulmonary artery intimal sarcoma is a rare malignancy mimicking pulmonary embolism, with clinical clues including disproportionately low d-dimer and characteristic CT findings like the 'wall eclipsing sign'.
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