Callata-Carhuapoma Hector R, Pato Cour Esperanza, Garcia-Paredes Beatriz, Fernandez Ramiro Mendez, Mendoza Fernandez Maria Luisa, Fernandez Aranzazu Manzano, De La Rosa Carlos Aguado, Sotelo Lezama Miguel J, Cabezas-Camarero Santiago, Sastre Varela Javier
Department of Medical Oncology, Hospital Clínico San Carlos, Madrid, Spain.
Department of Rheumatology, Hospital Clínico San Carlos, Madrid, Spain.
Pancreatology. 2015 Jul-Aug;15(4):440-4. doi: 10.1016/j.pan.2015.04.006. Epub 2015 Apr 24.
Pancreatic acinar cell carcinoma (PACC) is a rare pancreatic tumor, with an estimated frequency of less than 1% of pancreatic malignancies. There are no prospective studies to guide diagnostic or therapeutic algorithms. We report the case of a 36 year-old woman, diagnosed of a pancreatic tumor with liver and peritoneal metastases that was initially managed as a neuroendocrine tumor with temozolomide and capecitabine. After two cycles a severely painful arthritis developed in her left ankle with panniculitis and extensive fat necrosis, and CT scan demonstrated progressive disease. Pathology of the primary was reassessed establishing the diagnosis of PACC. The patient started treatment with FOLFIRINOX regimen, achieving clinical benefit and disease stabilization. We also briefly reviewed the literature on this rare subtype of pancreatic tumor.
胰腺腺泡细胞癌(PACC)是一种罕见的胰腺肿瘤,估计在胰腺恶性肿瘤中所占比例不到1%。目前尚无前瞻性研究来指导诊断或治疗方案。我们报告了一例36岁女性病例,该患者被诊断为患有肝和腹膜转移的胰腺肿瘤,最初被当作神经内分泌肿瘤用替莫唑胺和卡培他滨进行治疗。两个周期后,她的左脚踝出现了严重疼痛的关节炎,并伴有脂膜炎和广泛的脂肪坏死,CT扫描显示疾病进展。对原发灶进行病理重新评估后确诊为PACC。患者开始使用FOLFIRINOX方案治疗,获得了临床益处且疾病稳定。我们还简要回顾了关于这种罕见胰腺肿瘤亚型的文献。