Ramakrishna Banumathi, Yewale Rohan, Vijayakumar Kavita, Radhakrishna Patta, Ramakrishna Balakrishnan Siddartha
Department of Pathology, SRM Institutes for Medical Science, Vadapalani, India.
Department of Medical Gastroenterology, SRM Institutes for Medical Science, Vadapalani, India.
J Pathol Transl Med. 2020 May;54(3):258-262. doi: 10.4132/jptm.2020.02.10. Epub 2020 Mar 4.
IgG4-related disease of the stomach is a rare disorder, and only a few cases have been reported. We present two cases that were identified over a 2-month period in our center. Two male patients aged 52 and 48 years presented with mass lesion in the stomach, which were clinically thought to be gastrointestinal stromal tumor, and they underwent excision of the lesion. Microscopic examination revealed marked fibrosis, which was storiform in one case, associated with diffuse lymphoplasmacytic infiltration and an increase in IgG4-positive plasma cells on immunohistochemistry. Serum IgG4 level was markedly elevated. Although rare, IgG4-related disease should be considered in the differential diagnosis of gastric submucosal mass lesions.
胃IgG4相关性疾病是一种罕见的疾病,仅有少数病例报道。我们报告在我们中心2个月内确诊的2例病例。两名男性患者,年龄分别为52岁和48岁,均表现为胃内肿块,临床上认为是胃肠道间质瘤,他们接受了病变切除。显微镜检查显示明显纤维化,其中1例为席纹状,伴有弥漫性淋巴浆细胞浸润,免疫组化显示IgG4阳性浆细胞增多。血清IgG4水平显著升高。尽管罕见,但在胃黏膜下肿块病变的鉴别诊断中应考虑IgG4相关性疾病。