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Branchial Cleft Cyst Carcinoma Remains Grossly Over Diagnosed: A Large Database Analysis
Andrew Meci1, Neerav Goyal1,2, David Goldenberg1,2
1The Pennsylvania State University College of Medicine, Hershey, Pennsylvania, USA.
Most branchial cleft cyst carcinoma (BCCC) diagnoses are likely misdiagnoses of other head and neck cancers (HNC). This study suggests the BCCC diagnostic code should be discontinued due to poor survival rates and frequent misdiagnosis.
Area of Science:
- Oncology
- Head and Neck Surgery
- Pathology
Background:
- Branchial cleft cyst carcinomas (BCCC) are rare lateral neck malignancies.
- Primary BCCC diagnosis requires excluding cystic nodal metastasis.
- This study investigates BCCC diagnosis using a large database.
Purpose of the Study:
- To characterize the diagnosis of BCCC.
- To analyze patient demographics, treatments, and outcomes.
- To evaluate the accuracy of the BCCC diagnostic code.
Main Methods:
- Retrospective cohort study using the TriNetX Research database (2008-2018).
- Included patients aged ≥18 with ICD-10 C10.4 diagnosis.
- Analyzed demographics, oncologic history, diagnostic rates, and 5-year survival.
Main Results:
- 1070 BCCC patients identified; mean age 59.6, majority male and white.
- BCCC incidence rose until 2015, then dropped.
- 94.4% had another head and neck cancer (HNC) diagnosis within 5 years; 5-year survival was 56.0%.
Conclusions:
- The majority of BCCC patients were likely misdiagnosed with another HNC.
- Poor survival may result from delayed treatment due to misdiagnosis.
- The BCCC diagnostic code is considered detrimental and should be discontinued.
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