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Fibromatoses of Head and Neck: Case Series and Literature Review
OBJECTIVE: The objective of this study was to retrospectively review clinical data, management protocols, and clinical outcomes of patients with fibromatoses of head and neck region treated at our tertiary care center. METHODS: We retrospectively reviewed the medical records of 11 patients with conf...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rambam Health Care Campus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284993/ https://www.ncbi.nlm.nih.gov/pubmed/34270403 http://dx.doi.org/10.5041/RMMJ.10444 |
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author | Bhati, Muddasir Balakrishna, Gurukeerthi Joshi, Kamaldeep Bhattacharya, Kajari Bal, Munita Ghosh Laskar, Sarbani Sinha, Shwetabh Joshi, Amit Joshi, Poonam Nair, Sudhir Chaturvedi, Pankaj |
author_facet | Bhati, Muddasir Balakrishna, Gurukeerthi Joshi, Kamaldeep Bhattacharya, Kajari Bal, Munita Ghosh Laskar, Sarbani Sinha, Shwetabh Joshi, Amit Joshi, Poonam Nair, Sudhir Chaturvedi, Pankaj |
author_sort | Bhati, Muddasir |
collection | PubMed |
description | OBJECTIVE: The objective of this study was to retrospectively review clinical data, management protocols, and clinical outcomes of patients with fibromatoses of head and neck region treated at our tertiary care center. METHODS: We retrospectively reviewed the medical records of 11 patients with confirmed histopathological diagnosis of fibromatosis registered in the Department of Head and Neck Surgery at Tata Memorial Centre, India, between 2009 and 2019. Various clinical and pathological features and treatment modalities were evaluated. RESULTS: Age at diagnosis ranged between 18 and 74 years, with a median age of 36 years. The female-to-male ratio was 5:6. Supraclavicular fossa (n=4) was the most common subsite of origin in the neck (n=8). The lateral (n=2) and posterior cervical regions (n=2) were other common neck subsites. Less commonly involved sites were the mandible (n=1), maxilla (n=1), and thyroid (n=1). A total of eight patients underwent surgery at other centers before being referred to us for further management. Out of a total 11 patients, nine patients had unresectable disease at presentation. Six of the patients with unresectable disease received a combination of weekly doses of vinblastine 6 mg/m(2) and methotrexate 30 mg/m(2) for a median duration of 6 months (range 6–18 months) followed by hormonal therapy with tamoxifen. Three patients received metronomic chemotherapy followed by hormonal therapy. One treatment-naive patient with fibromatosis of posterior cervical (suboccipital) region underwent R2 resection (excision of bulk of the tumor with preservation of critical structures) at our center along with adjuvant radiotherapy. One pregnant patient reported to us after undergoing surgery outside and defaulting radiotherapy. During median follow-up of 29 months (range 1–77 months), six patients had stable disease, and four patients had disease reduction. Disease progression was seen in one patient. The two-year progression-free survival (PFS) was 90% (95% CI 70%–100%). CONCLUSION: Gross residual resection (R2) was the mainstay of surgical treatment in our series, as obtaining clear surgical margins is seldom possible in these locally aggressive tumors. Radiotherapy, chemotherapy, and hormonal therapy are the other preferred and more conservative treatment modalities. The goal of surgery should be preserving function with minimal or no morbidity. As fibromatoses in the head and neck region are extremely rare, their treatment awaits the development of standard treatment protocols. |
format | Online Article Text |
id | pubmed-8284993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rambam Health Care Campus |
record_format | MEDLINE/PubMed |
spelling | pubmed-82849932021-07-20 Fibromatoses of Head and Neck: Case Series and Literature Review Bhati, Muddasir Balakrishna, Gurukeerthi Joshi, Kamaldeep Bhattacharya, Kajari Bal, Munita Ghosh Laskar, Sarbani Sinha, Shwetabh Joshi, Amit Joshi, Poonam Nair, Sudhir Chaturvedi, Pankaj Rambam Maimonides Med J Original Research OBJECTIVE: The objective of this study was to retrospectively review clinical data, management protocols, and clinical outcomes of patients with fibromatoses of head and neck region treated at our tertiary care center. METHODS: We retrospectively reviewed the medical records of 11 patients with confirmed histopathological diagnosis of fibromatosis registered in the Department of Head and Neck Surgery at Tata Memorial Centre, India, between 2009 and 2019. Various clinical and pathological features and treatment modalities were evaluated. RESULTS: Age at diagnosis ranged between 18 and 74 years, with a median age of 36 years. The female-to-male ratio was 5:6. Supraclavicular fossa (n=4) was the most common subsite of origin in the neck (n=8). The lateral (n=2) and posterior cervical regions (n=2) were other common neck subsites. Less commonly involved sites were the mandible (n=1), maxilla (n=1), and thyroid (n=1). A total of eight patients underwent surgery at other centers before being referred to us for further management. Out of a total 11 patients, nine patients had unresectable disease at presentation. Six of the patients with unresectable disease received a combination of weekly doses of vinblastine 6 mg/m(2) and methotrexate 30 mg/m(2) for a median duration of 6 months (range 6–18 months) followed by hormonal therapy with tamoxifen. Three patients received metronomic chemotherapy followed by hormonal therapy. One treatment-naive patient with fibromatosis of posterior cervical (suboccipital) region underwent R2 resection (excision of bulk of the tumor with preservation of critical structures) at our center along with adjuvant radiotherapy. One pregnant patient reported to us after undergoing surgery outside and defaulting radiotherapy. During median follow-up of 29 months (range 1–77 months), six patients had stable disease, and four patients had disease reduction. Disease progression was seen in one patient. The two-year progression-free survival (PFS) was 90% (95% CI 70%–100%). CONCLUSION: Gross residual resection (R2) was the mainstay of surgical treatment in our series, as obtaining clear surgical margins is seldom possible in these locally aggressive tumors. Radiotherapy, chemotherapy, and hormonal therapy are the other preferred and more conservative treatment modalities. The goal of surgery should be preserving function with minimal or no morbidity. As fibromatoses in the head and neck region are extremely rare, their treatment awaits the development of standard treatment protocols. Rambam Health Care Campus 2021-07-20 /pmc/articles/PMC8284993/ /pubmed/34270403 http://dx.doi.org/10.5041/RMMJ.10444 Text en Copyright: © 2021 Bhati et al. https://creativecommons.org/licenses/by/3.0/This is an open-access article. All its content, except where otherwise noted, is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0 (https://creativecommons.org/licenses/by/3.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Bhati, Muddasir Balakrishna, Gurukeerthi Joshi, Kamaldeep Bhattacharya, Kajari Bal, Munita Ghosh Laskar, Sarbani Sinha, Shwetabh Joshi, Amit Joshi, Poonam Nair, Sudhir Chaturvedi, Pankaj Fibromatoses of Head and Neck: Case Series and Literature Review |
title | Fibromatoses of Head and Neck: Case Series and Literature Review |
title_full | Fibromatoses of Head and Neck: Case Series and Literature Review |
title_fullStr | Fibromatoses of Head and Neck: Case Series and Literature Review |
title_full_unstemmed | Fibromatoses of Head and Neck: Case Series and Literature Review |
title_short | Fibromatoses of Head and Neck: Case Series and Literature Review |
title_sort | fibromatoses of head and neck: case series and literature review |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284993/ https://www.ncbi.nlm.nih.gov/pubmed/34270403 http://dx.doi.org/10.5041/RMMJ.10444 |
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