Choi Sangjoon, Park Sujin, Chung Man Pyo, Kim Tae Sung, Cho Jong Ho, Han Joungho
Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
J Pathol Transl Med. 2019 May;53(3):188-191. doi: 10.4132/jptm.2019.02.21. Epub 2019 Mar 11.
IgG4-related disease is a systemic inflammatory disease and is known as IgG4-related lung disease (IgG4-RLD) when it involves the respiratory system. Primary lung cancer arising from a background of IgG4-RLD is very rare. Herein, we report a case of adenosquamous carcinoma arising from the background of IgG4-RLD and presenting as an interstitial lung disease pattern. A 66-year-old man underwent lobectomy under the impression of primary lung cancer. Grossly, the mass was ill-defined and gray-tan colored, and the background lung was fibrotic. Microscopically, tumor cells showed both squamous and glandular differentiation. Dense lymphoplasmacytic infiltration with fibrosis and obliterative phlebitis were seen in the background lung. IgG4 immunohistochemical stain showed diffuse positivity in infiltrating plasma cells. Primary lung adenosquamous carcinoma has not been reported in a background of IgG4-RLD. Due to the rarity of IgG4-RLD, physicians must follow patients with IgG4-RLD over long periods of time to accurately predict the risk of lung cancer.
IgG4相关性疾病是一种全身性炎症性疾病,当累及呼吸系统时被称为IgG4相关性肺病(IgG4-RLD)。IgG4-RLD背景下发生的原发性肺癌非常罕见。在此,我们报告一例起源于IgG4-RLD背景并表现为间质性肺病模式的腺鳞癌病例。一名66岁男性因原发性肺癌的诊断接受了肺叶切除术。大体上,肿块边界不清,呈灰棕色,背景肺组织纤维化。显微镜下,肿瘤细胞表现出鳞状和腺性分化。背景肺组织可见密集的淋巴细胞和浆细胞浸润伴纤维化及闭塞性静脉炎。IgG4免疫组化染色显示浸润的浆细胞弥漫阳性。IgG4-RLD背景下尚未见原发性肺腺鳞癌的报道。由于IgG4-RLD罕见,医生必须对IgG4-RLD患者进行长期随访,以准确预测肺癌风险。