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This case study presents a neonate diagnosed with a pulmonary mass, later confirmed as pulmonary sequestration. Born at term with significant respiratory distress, the infant was evaluated for differential diagnoses including pneumonia and intra/extralobar sequestration. Following imaging studies, surgical intervention was required to resect the mass, resulting in an uncomplicated recovery. The findings highlight the importance of timely diagnosis and management of congenital pulmonary anomalies in neonates.
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Pulmonary Mass in a Neonate Filomena Hazel R. Villa, MD PL 1- Pediatrics
Objective • To present a case of a neonate with pulmonary mass, its management and differential diagnoses
History • Boy M, 5 hours old • Born term (40 weeks), LGA (3732 g) • 21 y/o G1P1 • Prenatal History: unremarkable • Natal History: Born at CDN SROM - clear amniotic fluid, unknown amount NSVD, vertex presentation, APGAR 9,9
History • 2nd hour: feeding was started, + vomiting, tachypnea • 5th hour of life: persistence of tachypnea • Transferred to Thomason via EMS
Physical Examination • VS: T- 99.4; HR- 140; RR-89 BP - 57/33 (MAP 43-47) O2 Sat: 82-92% • Alert, and active • No icterus, no rashes • Open flat fontanelle • Eyes, normal shape and size with equal red reflex
Physical Examination • Ears: normally set, no gross anomalies • Nose: nares are patent, intact palate • Lungs and Chest: anteriorly - clear and equal breath sounds; posteriorly - slightly decreased breath sounds on the left hemithorax, ICS retractions, mild tachypnea
Physical Examination • Chest: normal rate and rhythm, pulses equal on all extremities, no murmur • Abdomen: umbilical stump: clean, with 3 vessels, soft, non tender, no organomegaly, no masses, normal bowel sounds • Genitalia: normal male genitalia
Physical Examination • Back and spine: no gross defects • Limbs and hips: no hip clicks, 10 fingers and toes, symmetric movements, capillary refill < 3 seconds • Neurologic: normal suck, tone, grasp, cry, Moro, root
Assessment and Plan • Term male infant • Suspected sepsis secondary to respiratory distress and desaturations • TTN vs Pneumonia • Plan: Sepsis work up, CXR • NPO, Isolette, Oxygen • Ampicillin and Gentamicin
Course in the NICU • Initial CXR: density in the left retrocardiac area • Unlikely pneumonia or atelectasis • Differential diagnoses: • Intra or Extra lobar sequestration • Mediastinal neuroblastoma • Broncho foregut malformation • Neuroenteric malformation • Intrathoracic kidneys
Course in the NICU • Case discussed with Radiologist • CT scan of the thorax • Ultrasound of abdomen and thorax • Echocardiogram: normal
Course in the NICU • CT scan of the thorax: • Soft tissue mass with no calcifications • No diaphragmatic eventration, no evidence of hernia • Differentials: Teratoma, Neuroblastoma
Course in the NICU • Sonogram of the abdomen: normal gas pattern, liver pancreas and kidneys-within the cavity • Sonogram of the thorax: • Left hemithorax mass • Arterial supply from the aorta • Vein drainage-origin not established • Consider: Extralobar Sequestration
Course in the NICU • 4th hospital day: referral to pediatric surgery • Images were reviewed • Plan: removal of the pulmonary mass
Course in the NICU • 5th hospital day: Surgery (Thoracotomy) • Intra-op findings: • Pulmonary sequestrum • Arterial aspect supplying the mass emerges from the thoracic aorta • Venous drainage into the intercostal vein • Resection of pulmonary sequestration
Post- operative Course • Uncomplicated recovery • Patient was discharged on 6th post-op day
Pathological Findings • It consists of a 6.5 x 4.5 x 3.0 cm lower lobe of lung tissue. It has an attached purple tan cystic structure filled with hemorrhagic serous fluid and air. This cystic structure measures 1.5 cm in greatest diameter. • Diagnosis: pulmonary sequestration with minimal interstitial lymphocytic inflammation dilated congested blood vessels and focal parenchymal hemorrhage.
Differential diagnoses • Pneumonia • Diaphragmatic hernia • Teratoma • Neuroblastoma • CCAM
Extralobar Pulmonary Sequestration • Non-functioning lung tissue • Aberrant blood supply- systemic circulation • Has its own pleura • Associated with other anomalies • Congenital
Extra vs Intralobar INTRALOBAR • Acquired/ congenital • Systemic blood supply • Pulmonary venous drainage • Pleura shared with adjacent normal lung EXTRALOBAR • Congenital • Systemic blood supply • Systemic venous drainage • Own pleura
Epidemiology • Incidence: 0.15-1.7% • 15-25%- extralobar • 75-85%- intralobar • 4:1 male to female • 60%- first 6 months of life
Prenatal Diagnosis and Treatment • No hydrops- follow closely with ultrasound • With hydrops- thoracoamniotic shunt • Postnatally- resection
Diagnosis • Plain x-ray- triangular or oval shape opacity • CT- cystic component • Color Doppler ultrasound- anomalous vessels • MRI- venous drainage
Treatment • Surgical resection • Thoracoscopy • Arterial embolization
Hemorrhage Empyema Hemothorax Hemoperitoneum Air leak Bronchopleural fistula Wound infection Atelectasis Infections Secretions management Respiratory failure Complications
Prognosis • With hydrops fetalis- dismal • Without hydrops - excellent
Baby boy M is presently being followed in our high risk clinic, growing and developing without significant pulmonary residuals.