Gupta Deepika, Khera Sudeep, Soni Subhash Chandra
Department of Pathology and Laboratory Medicine, All India Institute of Medical Sciences, Jodhpur, India.
Department of Surgical Gastroenterology, All India Institute of Medical Sciences, Jodhpur, India.
Ochsner J. 2022 Spring;22(1):89-93. doi: 10.31486/toj.21.0032.
Most malignant tumors arising from the biliary tract are adenocarcinomas. Adenosquamous carcinoma is an uncommon variant of extrahepatic bile duct cancer that is associated with more aggressive behavior than adenocarcinoma. A 58-year-old male presented with complaints of obstructive jaundice and dull aching pain in the abdomen. At his initial evaluation in another hospital, ultrasound of the abdomen and magnetic resonance cholangiopancreatography revealed common bile duct dilatation with an ill-defined lesion in the periampullary region. Endoscopic retrograde cholangiopancreatography showed infiltration of the ampulla. Biopsy specimen taken during stenting of the common bile duct suggested dysplasia. Because of recurrent jaundice, the patient was referred to our institution, and contrast-enhanced computed tomography (CT) of the abdomen showed a hypoenhancing lesion with ill-defined margins in the head of the pancreas. The patient underwent a Whipple procedure. Microscopic examination of the pancreaticoduodenectomy specimen showed an invasive adenosquamous tumor arising from the distal part of the common bile duct that infiltrated the body and head of the pancreas, involved the wall of the duodenum, and reached the duodenal mucosa. Morphologic diagnosis was supported by immunohistochemistry profile. Postoperative contrast-enhanced CT of the abdomen showed multiple enlarged mesenteric lymph nodes and multiple lesions in both lobes of the liver, suggestive of metastasis. The patient died 1 week after surgery. Because the clinical, pathologic, and prognostic characteristics of adenosquamous carcinoma are poorly known, early diagnosis of this rare entity is warranted for patient management.
大多数起源于胆道的恶性肿瘤是腺癌。腺鳞癌是肝外胆管癌的一种罕见变体,其行为比腺癌更具侵袭性。一名58岁男性因梗阻性黄疸和腹部隐痛就诊。在另一家医院进行初步评估时,腹部超声和磁共振胰胆管造影显示胆总管扩张,壶腹周围区域有边界不清的病变。内镜逆行胰胆管造影显示壶腹受侵。在胆总管支架置入期间获取的活检标本提示发育异常。由于黄疸复发,患者转诊至我院,腹部增强计算机断层扫描(CT)显示胰头有一个边界不清的低密度强化病变。患者接受了惠普尔手术。对胰十二指肠切除标本的显微镜检查显示,一个浸润性腺鳞肿瘤起源于胆总管远端,侵犯了胰腺体部和头部,累及十二指肠壁,并侵犯至十二指肠黏膜。免疫组化结果支持形态学诊断。术后腹部增强CT显示多个肠系膜淋巴结肿大以及肝脏两叶有多个病变,提示转移。患者术后1周死亡。由于腺鳞癌的临床、病理和预后特征鲜为人知,因此对于这种罕见疾病,有必要进行早期诊断以指导患者管理。