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Congenital ranula in a newborn: a rare presentation
Arvind Soni1, Pooja Suyal, Amit Suyal
1Indraprastha Apollo Hospitals, New Delhi, India.
Summary
This case report details a congenital ranula in a neonate, a rare cystic lesion in the floor of the mouth. Simple aspiration successfully treated the ranula, with no recurrence observed during follow-up.
Area of Science:
- Oral and Maxillofacial Surgery
- Pediatric Dentistry
- Congenital Anomalies
Background:
- Ranulas are rare cystic lesions originating in the floor of the mouth, typically presenting as either retention cysts or pseudocysts.
- These lesions result from mucus extravasation into surrounding tissues, often associated with salivary gland duct obstruction or trauma.
- Congenital ranulas, while uncommon, represent a specific subset requiring careful evaluation and management in neonates.
Observation:
- A full-term female neonate presented with a congenital ranula located on the left side of the floor of the mouth.
- The ranula was asymptomatic, causing no discomfort or complications, and therefore did not necessitate immediate intervention.
- The lesion's size and location were documented, noting its non-obstructive nature.
Findings:
- The congenital ranula in this neonate was successfully treated via aspiration using a wide-bore needle.
- Post-treatment follow-up at four months revealed no recurrence of the ranula.
- This minimally invasive approach proved effective for this specific case.
Implications:
- Congenital ranulas in neonates may be managed conservatively, with observation for spontaneous resolution in uncomplicated cases.
- Aspiration offers a simple, effective, and minimally invasive treatment option for symptomatic or persistent congenital ranulas.
- This case highlights the potential for successful non-surgical management of neonatal ranulas, avoiding more invasive procedures.
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Clinical Manifestations:
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