Mota Maria Emília, Lascane Nelise Alexandre Silva, Moreira Maria Stella, de Andrade Ariadne Padilha, Sedassari Bruno Tavares
Department of Stomatology, School of Dentistry, University of São Paulo (USP), São Paulo, SP, Brazil.
School of Dentistry, Municipal University of São Caetano do Sul, São Caetano do Sul, SP, Brazil.
Head Neck Pathol. 2025 Aug 12;19(1):103. doi: 10.1007/s12105-025-01836-5.
Cholangiocarcinoma is a malignant neoplasm with biliary differentiation and its metastatic spread to the oral and maxillofacial region is a rare event that can pose diagnostic challenges, especially when it is the initial presentation of the disease.
A 67-year-old woman presented with a painful and hard swelling in the right posterior aspect of the mandible with ulceration of the overlying mucosa. Radiological examination revealed a destructive lesion involving the body and angle of the mandible with cortical bone destruction. An incisional biopsy was performed.
The histopathology showed an invasive and moderately differentiated adenocarcinoma with tubular and cribriform patterns of growth. Neoplastic cells were diffusely positive to cytokeratin (CK) 7, to 35βH11, and weakly to 34βE12 on immunohistochemistry, but were negative to estrogen, progesterone, and androgen receptors, HepPar-1, CDX-2, CK20, GATA 3, napsin-A, PAX-8, TTF-1, CD117, DOG1, p63, and S100 protein. A preliminary diagnosis of metastatic adenocarcinoma was rendered, and the patient was referred to an oncologic evaluation. An abdominal computed tomography performed revealed an intrahepatic mass, diagnosed as a cholangiocarcinoma on core needle biopsy. The patient was submitted to palliative care and died of disease complications three months after the diagnosis of the mandibular lesion.
This case highlights the importance of an interdisciplinary approach, incorporating comprehensive clinical, pathological, and radiological correlations in reaching the appropriate diagnosis of a challenging metastatic lesion that developed in an unusual anatomical location.
胆管癌是一种具有胆管分化的恶性肿瘤,其转移至口腔颌面部区域是一种罕见事件,可能带来诊断挑战,尤其是当它作为疾病的初始表现时。
一名67岁女性,下颌骨右后方出现疼痛性硬性肿胀,覆盖黏膜溃疡。影像学检查显示下颌骨体部和角部有破坏性病变,伴有皮质骨破坏。进行了切开活检。
组织病理学显示为浸润性中度分化腺癌,呈管状和筛状生长模式。免疫组织化学检查显示肿瘤细胞对细胞角蛋白(CK)7、35βH11弥漫性阳性,对34βE12弱阳性,但对雌激素、孕激素和雄激素受体、HepPar-1、CDX-2、CK20、GATA 3、napsin-A、PAX-8、TTF-1、CD117、DOG1、p63和S100蛋白均为阴性。初步诊断为转移性腺癌,患者被转诊进行肿瘤学评估。腹部计算机断层扫描显示肝内有一肿块,经粗针活检诊断为胆管癌。患者接受了姑息治疗,在诊断下颌骨病变三个月后死于疾病并发症。
本病例强调了多学科方法的重要性,在对一个发生于不寻常解剖部位的具有挑战性的转移性病变进行准确诊断时,要综合临床、病理和影像学的相关性。