{"title":"头颈部纤维瘤病:病例系列及文献回顾。","authors":"Muddasir Bhati, Gurukeerthi Balakrishna, Kamaldeep Joshi, Kajari Bhattacharya, Munita Bal, Sarbani Ghosh Laskar, Shwetabh Sinha, Amit Joshi, Poonam Joshi, Sudhir Nair, Pankaj Chaturvedi","doi":"10.5041/RMMJ.10444","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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<sup>2</sup> and methotrexate 30 mg/m<sup>2</sup> 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%).</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":46408,"journal":{"name":"Rambam Maimonides Medical Journal","volume":"12 3","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2021-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8284993/pdf/","citationCount":"1","resultStr":"{\"title\":\"Fibromatoses of Head and Neck: Case Series and Literature Review.\",\"authors\":\"Muddasir Bhati, Gurukeerthi Balakrishna, Kamaldeep Joshi, Kajari Bhattacharya, Munita Bal, Sarbani Ghosh Laskar, Shwetabh Sinha, Amit Joshi, Poonam Joshi, Sudhir Nair, Pankaj Chaturvedi\",\"doi\":\"10.5041/RMMJ.10444\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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<sup>2</sup> and methotrexate 30 mg/m<sup>2</sup> 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%).</p><p><strong>Conclusion: </strong>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. 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引用次数: 1
摘要
目的:本研究的目的是回顾性回顾在我们三级保健中心治疗的头颈部纤维瘤患者的临床资料、治疗方案和临床结果。方法:回顾性分析2009年至2019年在印度塔塔纪念中心头颈外科登记的11例经组织病理学诊断为纤维瘤病的患者的病历。评估各种临床和病理特征及治疗方式。结果:诊断年龄在18 ~ 74岁之间,中位年龄36岁。男女比例为5:6。锁骨上窝(n=4)是颈部最常见的起病部位(n=8)。侧颈区(n=2)和后颈区(n=2)是其他常见的颈部亚位。较不常见的受累部位是下颌骨(n=1)、上颌骨(n=1)和甲状腺(n=1)。共有8名患者在转介到我们进行进一步治疗之前在其他中心接受了手术。在11例患者中,有9例患者在就诊时患有不可切除的疾病。6例不可切除的疾病患者接受每周剂量的长春碱6mg /m2和甲氨蝶呤30mg /m2的联合治疗,中位持续时间为6个月(范围6-18个月),随后接受他莫昔芬激素治疗。3例患者接受节律化疗后再进行激素治疗。一名未接受治疗的后颈椎(枕下)区纤维瘤病患者在我们中心接受了R2切除术(切除大部分肿瘤,保留关键结构)和辅助放疗。一名孕妇在接受室外手术和未接受放射治疗后向我们报告。中位随访29个月(1-77个月),6例患者病情稳定,4例患者病情减轻。1例患者出现疾病进展。两年无进展生存期(PFS)为90% (95% CI 70%-100%)。结论:由于在这些局部侵袭性肿瘤中很少有可能获得清晰的手术切缘,因此总的残余切除(R2)是我们系列手术治疗的主要方法。放疗、化疗和激素治疗是其他更保守的首选治疗方式。手术的目标应该是在保持功能的同时尽量减少或避免并发症。由于头颈部的纤维瘤病极为罕见,其治疗有待于标准治疗方案的发展。
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 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/m2 and methotrexate 30 mg/m2 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.