Thoracic Fluid Collection
Paula J. Woodward, MD
DIFFERENTIAL DIAGNOSIS
Common
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Bilateral Pleural Effusion
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Hydrothorax
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Unilateral Pleural Effusion
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Chylothorax
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Pericardial Effusion
Less Common
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Effusions Associated with Lung Masses
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Bronchopulmonary Sequestration
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Congential Cystic Adenomatoid Malformation (CCAM)
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Masses That Can Mimic Simple Fluid Collection
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Unilocular CCAM
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Congenital Diaphragmatic Hernia
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ESSENTIAL INFORMATION
Key Differential Diagnosis Issues
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First determine where the fluid is located
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Pleural space, pericardial space or within a mass
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Pleural effusion
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Routine four chamber heart view
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Curvilinear, anechoic fluid
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Echogenic lung displaced medially
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Coronal chest view
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Lung displaced superiorly and medially
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“Wing-like” lungs float in fluid
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Pericardial effusion
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Fluid collection surrounds fetal heart
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If large, heart is seen beating in a “bag of water”
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Lungs will be compressed posteriorly, not free floating
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Large, unilocular cystic masses may simulate pleural effusion
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Masses are rounded or ovoid
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Have mass effect on lungs and mediastinal structures
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Lung shifted away from fluid, not surrounded by fluid as in a pleural effusion
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Helpful Clues for Common Diagnoses
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Hydrothorax
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Serous fluid collection
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Effusions are bilateral and symmetric
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Hallmark finding in hydrops fetalis (both immune and nonimmune)
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Hydrops defined as fluid accumulation in 2 or more body cavities
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Pleural effusion
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Ascites
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Skin edema
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Pericardial fluid
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Polyhydramnios and placentomegaly also often present if there is hydrops
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Anomalies commonly associated with effusions/hydrops
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Cystic hygroma (Turner syndrome) most common
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Trisomy 21 (other markers usually seen); trisomy 18, 13 less likely
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Cardiac defects
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Cardiac arrhythmia
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Infection
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Cystic adenomatoid malformation (< 10% have hydrops)
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Fetal masses causing high output failure (and possible hydrops)
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Sacrococcygeal teratoma
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Goiter
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Vascular shunting: Vein of Galen malformation, arteriovenous fistulas, hepatic hemangioendothelioma, placental chorioangioma
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First trimester pleural effusion
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Can be seen as early as 7 weeks
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Associated with increased nuchal translucency
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Poor prognosis when present before 15 wks
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Aneuploidy common: Turner syndrome most likely
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Chylothorax
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Chylous fluid collection
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Effusion is unilateral
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Primary congenital lymphatic defect
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Atresia, fistula, or absence of thoracic duct
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Thoracic duct crosses from right to left at 5th thoracic level
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Level of obstruction determines right versus left-sided effusion
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Equal incidence of right and left-sided effusions
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Fluid is anechoic
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Only after neonatal feeding will chylous fluid appear “milky”
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Mass effect common
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Mediastinal shift
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Flattened diaphragm
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May lead to hydrops when large
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Consider performing fetal thoracentesis if evidence of fetal compromise
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5% associated with aneuploidy
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Turner syndrome
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Trisomy 21
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Noonan syndrome
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Amniocentesis warranted
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15% resolve in fetal life
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Near 100% survival without hydrops and normal chromosomes
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Pericardial Effusion
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Seen best on standard four chamber view
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Lenticular or oval collection of fluid adjacent to, or surrounding heart
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Trace of fluid along one ventricular wall is normal
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Can be up to 2 mm
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Majority of fetuses (50-80%) have trace fluid if careful search done
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Generally transient
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If fetus not at increased risk, follow-up not necessary
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Significant effusion if fluid surrounds atria as well as ventricles
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Pericardial effusion seen in many conditions
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Evaluate heart for structural abnormality, arrhythmia or mass
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Look for other signs of hydrops
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Look for signs of congenital infection
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Look for anemia
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Helpful Clues for Less Common Diagnoses
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Bronchopulmonary Sequestration
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6-10% may develop unilateral pleural effusion
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May cause tension hydrothorax requiring fetal thoracentesis to decompress
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90% left-sided
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Look for triangular, solid mass surrounded by pleural fluid
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Congenital Cystic Adenomatoid Malformation (CCAM)
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May see effusions if fetus develops hydrops
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Occurs in < 10% of cases
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Unilocular CCAM can appear as a simple fluid collection
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Look for stomach below diaphragm to rule out congenital diaphragmatic hernia
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Congenital Diaphragmatic Hernia
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