CASE 13162 Published on 18.02.2016

A strange case of pulmonary embolism

Section

Chest imaging

Case Type

Clinical Cases

Authors

Robella Mattia1, Cortese Giancarlo2, Bertucci Roberto3

1 Radiology Institute, Surgical Science Department, University of Torino, City of Health and Science, Torino, Via Genova 3
2 Radiology Department, Maria Vittoria Hospital, Torino
3 Infective Disease 2 Department, Amedeo di Savoia Hospital, Torino
Patient

78 years, male

Categories
Area of Interest Thorax, Abdomen ; Imaging Technique Conventional radiography, CT
Clinical History
A 78-year-old man, ex-smoker, in treatment with oral anticoagulants for permanent atrial fibrillation was referred for a chest X-ray in order to investigate an episode of haemoptysis, longstanding cough and recurrent bronchitis. A hepatic cyst, probably hydatid in nature, was identified during preoperative assessment for elective cholecystectomy 20 years ago.
Imaging Findings
Chest X-ray (Fig. 1) demonstrated multiple nodular opacities in the right upper lobe.
Contrast enhanced Chest-CT demonstrated the presence of filling defects in the right middle and inferior lobe pulmonary arteries, compatible with embolism (Fig. 2a-b). Lobulated non-calcified opacities in bilateral upper lobes and left lower lobes were noted. These structures correspond to dilated segmental and subsegmental pulmonary arteries, filled with hypodense material (Fig. 2c-d). Echocardiography showed no signs of increased right ventricular pressure.
A partially calcified multi-loculated cyst was detected in liver segments III-IV, compatible with echinococcal cyst, the left hepatic vein could not be delineated (Fig. 2d-e).
PET-CT showed intense uptake of 18F-FDG at the level of the nodes (max SUV 4, 4), without other signs of increased metabolic activity.
Discussion
Embolization of echinococcal cysts to pulmonary arteries is rare [1-3] and it is caused by hepatic cysts in communication with hepatic veins/inferior vena cava or ruptured cysts in right cardiac chambers [2-5]. Arterial obstruction results from daughter cysts without thrombosis and is classified as a non-thrombotic pulmonary arterial embolism [2, 5]). In our case, infiltration of the left hepatic vein resulted in diffuse pulmonary arterial tree embolization without significant involvement of lung parenchyma.
The main clinical symptoms are cough, dyspnoea, haemoptysis and acute chest pain [6].
Patients with these symptoms are usually referred to the Radiology Department for Chest CT to rule out pulmonary thromboembolism. Enhanced CT demonstrates occlusion and enlargement of the pulmonary arterial tree by hypodense content; the differential diagnosis can therefore be other causes of embolism (thrombotic, septic and neoplastic) and pulmonary artery sarcoma. Clinical history (knowledge of hydatid infestation) and presentation are essential to achieve the correct diagnosis. When hydatid embolism is suspected, radiologists should search for the source of the emboli (hepatic cysts in communication with hepatic veins/vena cava, ruptured cyst in the right cardiac chambers).
MRI can be useful in the differential diagnosis, demonstrating the high signal in the T2-weighted sequences typical of cysts.
Pulmonary artery sarcoma is characterized by low-attenuating filling defect which can extend into lung parenchyma or mediastinum and shows diffuse enhancement.
Cases of hydatid pulmonary embolism are classified into three groups accordig to clinical course: acute fatal cases, subacute pulmonary hypertension cases resulting in death within 1 year and chronic pulmonary hypertension cases [2, 5, 7]. Our patient did not present with severe acute symptoms, neither did he develop chronic pulmonary hypertension. The patient is being regularly followed with echocardiography and shows no signs of increasing right ventricle pressure.
To confirm our diagnosis, the patient underwent VATS biopsy: a diagnosis of gigantocellular fibrogranulomatous nodules with ischemic necrosis and exogenous material referable to fragments of parasites was made.
Treatment of choice for hydatid pulmonary embolism is surgery. Given the anesthesiologic risk due to the permanent atrial fibrillation and the surgical risk of rupture of the artery or of the cyst with anaphylactic shock, we decided on repeated cycles of albendanzole and follow-up, in agreement with the patient.
After 2 years the patient reports a substantial stability in his symptomatology. The last follow up CT (Fig 3a-b) showed an increased extent of pulmonary arterial tree involvement; albendanzole therapy was then again started.
Differential Diagnosis List
Echinococcal pulmonary circulation embolism
Pulmonary thromboembolism
Pulmonary artery Sarcoma
Septic embolism
Tumor embolism
Final Diagnosis
Echinococcal pulmonary circulation embolism
Case information
URL: https://www.eurorad.org/case/13162
DOI: 10.1594/EURORAD/CASE.13162
ISSN: 1563-4086
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