NewYork-Presbyterian Weill Cornell Medical Center, New York, NY, USA.
Int J Surg Pathol. 2020 Sep;28(6):668-671. doi: 10.1177/1066896920905887. Epub 2020 Feb 12.
Sarcoid-like granulomatosis is a known but rare adverse reaction to immune checkpoint inhibitors and chemotherapy in the treatment of advanced solid tumors. We present a case of a 29-year-old female with a pathologically confirmed poorly differentiated invasive ductal carcinoma of the breast with presumed metastases to the lungs, hilar lymph nodes, liver, and spleen. Despite appropriate chemotherapy, the patient developed pulmonary lesions that were interpreted on imaging studies as progression of malignancy. Autopsy revealed disseminated sarcoid-like granulomatosis with multiple noncaseating granulomata with associated fibrosis in the lungs, liver, and spleen. No residual invasive carcinoma or metastatic disease was identified. This case illustrates the difficulty in differentiating this nonneoplastic process from progressive disease in the clinical setting.
类肉瘤样肉芽肿病是一种已知但罕见的不良反应,发生于免疫检查点抑制剂和化疗治疗晚期实体瘤的过程中。我们报告了 1 例 29 岁女性,其病理证实为乳腺低分化浸润性导管癌,伴肺、肺门淋巴结、肝和脾转移的假定。尽管进行了适当的化疗,但该患者出现了肺部病变,影像学研究提示为恶性肿瘤进展。尸检显示肺部、肝脏和脾脏弥漫性类肉瘤样肉芽肿病,伴有多个非干酪样肉芽肿和相关纤维化。未发现残留的浸润性癌或转移性疾病。该病例说明了在临床环境中区分这种非肿瘤过程与进行性疾病的困难。