CARCINOMA EX PLEOMORPHIC ADENOMA: DIAGNOSTIC CHALLENGE AND TREATMENT PROTOCOL

IF 1.8 Q3 HEMATOLOGY
Suad Enaami , Ebtihaj Hassan , Jalal Eltabib
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Abstract

Objective

Carcinoma ex pleomorphic adenoma CXPA, a rare epithelial malignancy arising from a primary or recurrent benign pleomorphic adenoma, accounts for 11.% of all malignant salivary gland neoplasms. It is difficult to diagnose preoperatively. often poses a diagnostic challenge to clinicians and pathologists Treatment involves an ablative surgical procedure with neck dissection followed by radiotherapy. We aim to investigate the impact of postoperative radiotherapy on improving disease-free survival.

Case report

A 39-year-old Libyan male presented with painless swelling near the angle of the right mandible four months ago. FNA Cytology showed a benign pleomorphic adenoma. A total parotidectomy with VII CN preservation was done in September 2022. The histopathological features were consistent with carcinoma EX pleomorphic adenoma, a widely invasive salivary duct carcinoma grade III with < 1mm(close)margins staged PT1 N0 M0. The immunohistochemistry revealed the negative expression of ER and PR assays.

Methodology

In December 2022, he received adjuvant radiation to the tumor bed (66 GY) in 33 fractions over 6 weeks based on the VMAT technique. 12-month follow-up, the patient showed no evidence of local or regional disease recurrence or distant metastasis.

Results

Radical surgery, followed by adjuvant radiotherapy, should be considered the standard of care for a patient, with significant improvement in 5-year locoregional control. and in general, salivary gland neoplasms respond poorly to chemotherapy and are currently indicated only for palliative sitting. More prospective data is needed to establish a role for hormonal therapy and molecularly targeted therapies.

Conclusion

CXPA is an uncommonly aggressive malignancy that, if associated with regional metastasis, invariably leads to mortality. Total resection of the tumor, followed by adjuvant radiotherapy, should be considered the standard of care for a patient with significantly improved 5-year locoregional control. Early and prompt diagnosis, followed by aggressive surgical intervention and adjuvant radiotherapy for patients with carcinoma ex pleomorphic adenoma, can enhance their survival rates.

癌前多形性腺瘤:诊断挑战和治疗方案
摘要: 多形性腺瘤癌(CXPA)是一种罕见的上皮性恶性肿瘤,由原发性或复发性良性多形性腺瘤引起,占所有唾液腺恶性肿瘤的 11.%。它很难在术前确诊,常常给临床医生和病理学家带来诊断上的挑战。 治疗包括颈部切除的消融外科手术和放疗。我们旨在研究术后放疗对提高无病生存率的影响。病例报告一名 39 岁的利比亚男性四个月前出现右下颌角附近无痛性肿胀。FNA 细胞学检查显示为良性多形性腺瘤。2022 年 9 月,该患者接受了腮腺全切除术,并保留了第七CN。组织病理学特征与癌EX多形性腺瘤一致,为广泛浸润性涎管癌III级,边缘< 1毫米(近),分期为PT1 N0 M0。2022 年 12 月,他接受了基于 VMAT 技术的肿瘤床辅助放射治疗(66 GY),分 33 次,每次 6 周。12个月的随访显示,患者没有出现局部或区域性疾病复发或远处转移的迹象。结果对患者来说,先进行放射外科手术,再进行辅助放疗,应被视为标准治疗方法,可显著改善5年的局部区域控制。结论CXPA是一种不常见的侵袭性恶性肿瘤,如果伴有区域转移,必然会导致死亡。肿瘤全切除术和辅助放疗应被视为标准治疗方法,可显著改善患者的 5 年局部控制率。对多形性腺瘤外癌患者进行早期和及时诊断,然后进行积极的手术干预和辅助放疗,可以提高患者的生存率。
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来源期刊
CiteScore
2.40
自引率
4.80%
发文量
1419
审稿时长
30 weeks
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