Brandenburg Tim, Muchalla Philipp, Theurer Sarah, Schmid Kurt Werner, Führer Dagmar
Department of Endocrinology, Diabetes and Metabolism, Endocrine Tumour Center at West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Endocrine Tumour Center at West German Cancer Center, Member of ENDO-ERN and EURACAN, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Eur Thyroid J. 2021 Nov;10(6):511-516. doi: 10.1159/000518055. Epub 2021 Sep 3.
Primary squamous cell carcinoma (PSCC) of the thyroid is an exceptionally rare malignancy accounting for <1% of all primary thyroid cancers. Therapy is multimodal including surgery, radiotherapy, and chemotherapy but with no consensus for management and therapy. Here, we describe a case of a male patient who presented with a BRAF V600E-mutated PSCC of the thyroid gland showing response to combined dabrafenib and trametinib therapy over a period of >12 months.
A 78-year-old male patient presented with a 3-week history of dysphonia and dyspnoea. Laryngoscopy revealed a mechanical obstruction by a right-sided, subglottical mass, which on cervical ultrasound was highly suggestive of anaplastic thyroid carcinoma. Additional workup including esophagogastroduodenoscopy showed compression of the oesophagus but no oesophageal infiltration by the tumour. Immunohistochemistry displayed CK19-positive cells indicating epithelial origin of the tumour. CK5/6 and P40 immunohistochemistry confirmed the morphological impression of squamous cell differentiation while staining with thyroid markers TTF-1 and TPO was negative and PAX8 showed a nuclear positive signal. Based on immunohistopathology, presence of TP53 and BRAF V600E mutations, and exclusion of metastatic squamous cell carcinoma of other origin, the diagnosis of a PSCC of the thyroid was established. As an individualized treatment concept, we decided to advocate combined BRAF V600E targeting by the multikinase inhibitors dabrafenib and trametinib. This led to drastic improvement in patient's quality of life without severe side effects over a period of >12 months.
In this case, molecular diagnosis allowed a highly individualized treatment concept with combined dabrafenib and trametinib therapy.
甲状腺原发性鳞状细胞癌(PSCC)是一种极为罕见的恶性肿瘤,占所有原发性甲状腺癌的比例不到1%。治疗方式为多模式,包括手术、放疗和化疗,但在管理和治疗方面尚无共识。在此,我们描述一例男性患者,其患有BRAF V600E突变的甲状腺PSCC,在超过12个月的时间里对达拉非尼和曲美替尼联合治疗有反应。
一名78岁男性患者出现声音嘶哑和呼吸困难3周病史。喉镜检查发现右侧声门下肿物导致机械性梗阻,颈部超声高度提示为未分化甲状腺癌。包括食管胃十二指肠镜检查在内的进一步检查显示食管受压,但肿瘤未侵犯食管。免疫组织化学显示CK19阳性细胞,表明肿瘤起源于上皮。CK5/6和P40免疫组织化学证实了鳞状细胞分化的形态学印象,而甲状腺标志物TTF-1和TPO染色为阴性,PAX8显示核阳性信号。基于免疫组织病理学、TP53和BRAF V600E突变的存在以及排除其他来源的转移性鳞状细胞癌,确诊为甲状腺PSCC。作为个体化治疗方案,我们决定采用多激酶抑制剂达拉非尼和曲美替尼联合靶向BRAF V600E。这使得患者的生活质量在超过12个月的时间里得到显著改善,且无严重副作用。
在本病例中,分子诊断使得采用达拉非尼和曲美替尼联合治疗的高度个体化治疗方案成为可能。