Hirota T, Kaneda M, Iwasa M, Tamaki H
Department of Surgery, Mie Prefectural Hospital of Shima, Mie, Japan.
Surg Today. 1993;23(9):810-5. doi: 10.1007/BF00311625.
Epithelioid cell granulomas identical to those of systemic sarcoidosis are occasionally observed within malignant neoplasms, particularly in the lymphatics draining a primary tumor. These histologic changes have been termed sarcoid reactions and are easily confused with systemic sarcoidosis. This report describes an extremely rare case of gastric cancer accompanied by sarcoid reactions in the regional lymph nodes and liver parenchyma near a tumor metastasis. A 63-year-old woman with advanced gastric cancer was treated by subtotal gastrectomy with dissection of the regional lymph nodes and local excision of the liver tissue involved by metastasis. Microscopic examination of the resected lymph nodes and liver disclosed the presence of sarcoid-like granulomas. The absence of any clinical manifestations and the negative results of the Kveim test, chest radiograph, and laboratory tests, including that for the serum angiotensin converting enzyme excluded the possibility of systemic sarcoidosis. The presence of a sarcoid reaction in the liver parenchyma adjacent to a metastasis has never been reported previously.
在恶性肿瘤内偶尔可观察到与系统性结节病相同的上皮样细胞肉芽肿,尤其是在引流原发性肿瘤的淋巴管中。这些组织学改变被称为结节病反应,很容易与系统性结节病混淆。本报告描述了一例极为罕见的胃癌病例,其区域淋巴结和肿瘤转移附近的肝实质伴有结节病反应。一名63岁的晚期胃癌女性接受了胃次全切除术,包括区域淋巴结清扫和转移灶累及的肝组织局部切除。对切除的淋巴结和肝脏进行显微镜检查发现存在类结节状肉芽肿。无任何临床表现,且Kveim试验、胸部X线片及实验室检查(包括血清血管紧张素转换酶检测)结果均为阴性,排除了系统性结节病的可能性。此前从未有过肝实质转移灶附近出现结节病反应的报道。