Related Experiment Video
Updated: Jun 2, 2026

19:53
Single-stage Dynamic Reanimation of the Smile in Irreversible Facial Paralysis by Free Functional Muscle Transfer
Published on: March 1, 2015
105.8K
Parotid abscess causing facial palsy in a child: A case report
Samia Meherzi1, Amin Khbou1, Leila Jerbi1
1ENT Department, Hospital of Sidi Bouzid, Sidi Bouzid, Tunisia; University of Sousse, Faculty of Medicine of Sousse, Tunisia.
International Journal of Surgery Case Reports
|October 6, 2024
Summary
This case report details a rare pediatric parotid abscess causing facial palsy. Early antibiotic treatment and surgical drainage led to significant facial nerve recovery.
Area of Science:
- Pediatric Otolaryngology
- Infectious Diseases
- Neurology
Background:
- Parotid abscesses are uncommon in children.
- Facial nerve palsy secondary to parotid abscess is exceptionally rare.
Observation:
- A healthy 12-year-old presented with acute parotid swelling and Grade IV facial palsy.
- Staphylococcus aureus was identified as the causative agent.
- The patient received intravenous antibiotics and surgical drainage.
Findings:
- The parotid abscess and swelling resolved with treatment.
- Facial nerve function improved significantly, grading II on the House-Brackmann scale.
- Complete recovery was observed in this case of incomplete paralysis.
Implications:
- Early, targeted antibiotic therapy and surgical intervention are crucial for favorable outcomes.
- Prompt management can significantly improve facial motor function recovery in pediatric parotid abscess cases.
- Clinical expertise in managing this rare complication is vital for pediatricians and otolaryngologists.
Related Concept Videos
The Retinoblastoma Gene
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
Prosopagnosia
Prosopagnosia, also known as face blindness, is the inability to recognize faces. In severe cases, individuals with prosopagnosia may not recognize close family members, including parents and spouses, by their faces. For instance, someone with prosopagnosia might walk past their child in a crowd, only realizing their mistake upon noticing their child's distinctive backpack or favorite jacket. Prosopagnosia specifically impairs facial recognition, while the recognition of other objects or...
Respiratory Syncytial Virus Disease
Human respiratory syncytial virus (RSV) is a widespread pathogen that primarily targets infants and young children but also poses a serious health risk to elderly and immunocompromised individuals. Belonging to the Pneumoviridae family, RSV is a negative-sense, single-stranded RNA virus within the Pneumovirus genus. Its global health burden is significant, with millions of cases annually resulting in hospitalizations and mortality, particularly in resource-limited settings. Although most...

