Lipoblastoma of the infratemporal pterygoid region: An unusual case report

Lipoblastoma is a rare, benign tumor that arises from embryonic adipose tissue. It is more commonly found in males and is typically diagnosed in children under the age of 5. The tumor can occur in the head and neck region, including the cheek, jaw, and neck. Treatment involves complete surgical removal of the tumor. We present the clinical case of a lipoblastoma located in the pterygoid region, which has never been described before in the literature. The tumor was surgically treated using a transnasal transpterygoid endoscopic approach. An 11-year-old female patient presented to our hospital with a history of persistent, diffuse headaches lasting for 3 years, accompanied by nausea, vomiting, and intolerance to lights and sounds. A brain MRI revealed a lesion in the right pterygoid fat. A CT scan was performed to assess the bony structures. Nasal endoscopy was normal. The patient underwent radical surgery under general anesthesia, with a transnasal transpterygoid endoscopic approach and reconstruction using a rescue flap. Pathological analysis confirmed the diagnosis of lipoblastoma. The postoperative course was uneventful and 3 months after surgery the patient reported no further headache. The patient was followed up for 5 years post-surgery, with no evidence of recurrence. The transnasal transpterygoid endoscopic approach is a safe and effective technique, even in pediatric patients, but it should only be performed by a qualified and experienced surgeon. Although lipoblastoma is an extremely rare tumor, it should be considered in the differential diagnosis of headache in children. • First reported case of lipoblastoma in the pterygoid region. • Pediatric patient successfully treated with a transnasal transpterygoid endoscopic approach. • Complete tumor resection achieved with no recurrence after 5 years. • Endoscopic surgery shown to be safe and effective for deep-seated head and neck tumors. • Lipoblastoma should be considered in the differential diagnosis of pediatric headaches

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Journal
Otolaryngology Case Reports
Published
2025-09-23
DOI
https://doi.org/10.1016/j.xocr.2025.100704
Primary Topic
Tumors and Oncological Cases
Type
article
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article

Lipoblastoma of the infratemporal pterygoid region: An unusual case report

Luca Guastini, Marta De Vecchi, Diego Criminelli Rossi, Frank Rikki Canevari et al.
Otolaryngology Case Reports
Tumors and Oncological Cases
article

Lipoblastoma of the infratemporal pterygoid region: An unusual case report

Luca Guastini, Marta De Vecchi, Diego Criminelli Rossi, Frank Rikki Canevari, Melania Bertolini, Monica Feltri
article en

Abstract

Lipoblastoma is a rare, benign tumor that arises from embryonic adipose tissue. It is more commonly found in males and is typically diagnosed in children under the age of 5. The tumor can occur in the head and neck region, including the cheek, jaw, and neck. Treatment involves complete surgical removal of the tumor. We present the clinical case of a lipoblastoma located in the pterygoid region, which has never been described before in the literature. The tumor was surgically treated using a transnasal transpterygoid endoscopic approach. An 11-year-old female patient presented to our hospital with a history of persistent, diffuse headaches lasting for 3 years, accompanied by nausea, vomiting, and intolerance to lights and sounds. A brain MRI revealed a lesion in the right pterygoid fat. A CT scan was performed to assess the bony structures. Nasal endoscopy was normal. The patient underwent radical surgery under general anesthesia, with a transnasal transpterygoid endoscopic approach and reconstruction using a rescue flap. Pathological analysis confirmed the diagnosis of lipoblastoma. The postoperative course was uneventful and 3 months after surgery the patient reported no further headache. The patient was followed up for 5 years post-surgery, with no evidence of recurrence. The transnasal transpterygoid endoscopic approach is a safe and effective technique, even in pediatric patients, but it should only be performed by a qualified and experienced surgeon. Although lipoblastoma is an extremely rare tumor, it should be considered in the differential diagnosis of headache in children. • First reported case of lipoblastoma in the pterygoid region. • Pediatric patient successfully treated with a transnasal transpterygoid endoscopic approach. • Complete tumor resection achieved with no recurrence after 5 years. • Endoscopic surgery shown to be safe and effective for deep-seated head and neck tumors. • Lipoblastoma should be considered in the differential diagnosis of pediatric headaches

Otolaryngology Case ReportsVol. 37
Martin University (US), Ospedale Policlinico San Martino (IT), University of Genoa (IT)
Openalex Percentile: Top 63%
Tumors and Oncological Cases
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