Pediatric SMARCB1 (INI1)–Deficient Parapharyngeal Myoepithelial Carcinoma: A Stair-Step Mandibulotomy Approach and Case Report

Background: SMARCB1 (INI-1)–deficient myoepithelial carcinoma of soft tissue is an exceptionally rare and aggressive pediatric neoplasm. Although epithelial in origin, these tumors display sarcoma-like behavior and often arise in the head and neck, where complete surgical excision can be technically challenging. Here, we present a complex case where multidisciplinary management was necessary for a complete tumor resection utilizing a novel mandibulotomy approach to help achieve an R0 tumor resection. Case Description: A 3-year-old female presented with progressive left neck swelling, with imaging demonstrating a 5.6 cm retropharyngeal mass displacing the carotid space. An open biopsy revealed a SMARCB1 (INI-1)–deficient myoepithelial carcinoma, confirmed through molecular testing and secondary review at an outside research hospital. PET-CT showed no evidence of metastatic disease. The patient underwent 6 cycles of modified CHOP-based chemotherapy (vincristine, cyclophosphamide, doxorubicin) with a near-complete metabolic response. Definitive surgical management included radical tumor resection requiring a stair-step mandibulotomy with selective neck dissection and carotid artery resection following preoperative embolization. Tracheostomy and gastrostomy were performed concurrently. Facial, vagus, and hypoglossal nerves were preserved. Postoperatively, the patient had a left-sided stroke requiring physiotherapy and speech-language therapy, but now has almost complete recovery. Adjuvant proton beam radiotherapy was added to the current chemotherapy. The patient continues with follow-up, demonstrating good outcomes and tolerating the treatment. Conclusion: This case illustrates the diagnostic and surgical complexities of SMARCB1-deficient myoepithelial carcinoma in the pediatric parapharyngeal space. Early multidisciplinary collaboration and tailored multimodal therapy are critical to optimizing outcomes while preserving neurovascular function.

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FACE
Published
2026-11-01
DOI
https://doi.org/10.1177/27325016261500642
Primary Topic
Sarcoma Diagnosis and Treatment
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article
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article

Pediatric SMARCB1 (INI1)–Deficient Parapharyngeal Myoepithelial Carcinoma: A Stair-Step Mandibulotomy Approach and Case Report

Joseph Lopez, Ajay Bharathan, Gabriela Cendejas, Kian Darius Tartibi et al.
FACE
Sarcoma Diagnosis and Treatment
article

Pediatric SMARCB1 (INI1)–Deficient Parapharyngeal Myoepithelial Carcinoma: A Stair-Step Mandibulotomy Approach and Case Report

Joseph Lopez, Ajay Bharathan, Gabriela Cendejas, Kian Darius Tartibi, Maria Jose Polania-Sandoval
article en

Abstract

Background: SMARCB1 (INI-1)–deficient myoepithelial carcinoma of soft tissue is an exceptionally rare and aggressive pediatric neoplasm. Although epithelial in origin, these tumors display sarcoma-like behavior and often arise in the head and neck, where complete surgical excision can be technically challenging. Here, we present a complex case where multidisciplinary management was necessary for a complete tumor resection utilizing a novel mandibulotomy approach to help achieve an R0 tumor resection. Case Description: A 3-year-old female presented with progressive left neck swelling, with imaging demonstrating a 5.6 cm retropharyngeal mass displacing the carotid space. An open biopsy revealed a SMARCB1 (INI-1)–deficient myoepithelial carcinoma, confirmed through molecular testing and secondary review at an outside research hospital. PET-CT showed no evidence of metastatic disease. The patient underwent 6 cycles of modified CHOP-based chemotherapy (vincristine, cyclophosphamide, doxorubicin) with a near-complete metabolic response. Definitive surgical management included radical tumor resection requiring a stair-step mandibulotomy with selective neck dissection and carotid artery resection following preoperative embolization. Tracheostomy and gastrostomy were performed concurrently. Facial, vagus, and hypoglossal nerves were preserved. Postoperatively, the patient had a left-sided stroke requiring physiotherapy and speech-language therapy, but now has almost complete recovery. Adjuvant proton beam radiotherapy was added to the current chemotherapy. The patient continues with follow-up, demonstrating good outcomes and tolerating the treatment. Conclusion: This case illustrates the diagnostic and surgical complexities of SMARCB1-deficient myoepithelial carcinoma in the pediatric parapharyngeal space. Early multidisciplinary collaboration and tailored multimodal therapy are critical to optimizing outcomes while preserving neurovascular function.

FACE
University of Central Florida (US), AdventHealth for Children (US)
Openalex Percentile: Top 12%
Sarcoma Diagnosis and Treatment
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