Oshitari Toshiyuki, Yotsukura Jiro, Asahagi Kaoru, Baba Takayuki, Kishimoto Takashi, Yamamoto Shuichi
Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
Clin Ophthalmol. 2010 Dec 30;5:23-5. doi: 10.2147/OPTH.S16303.
The purpose of this study is to present a case of chronic sclerosing dacryoadenitis with high level of IgG4 in a patient diagnosed earlier with Castleman disease. A 79-year-old man noticed a swelling of his lower left jaw that was first seen 8 years earlier. He was diagnosed with Castleman disease from the histopathological examination of a biopsy of the submandibular gland. Since then, the size of the gland had not changed, and he had no systemic inflammatory signs or symptoms. He developed diplopia a year earlier, and CT scans showed bilateral swelling of the lacrimal glands. He was referred to our hospital for further examinations. The patient underwent partial dacryoadenectomy. From the histopathological examinations, he was diagnosed with chronic sclerosing dacryoadenitis with high level of the serum IgG4. He underwent oral steroid therapy and the swollen lacrimal glands were significantly improved. The results suggest that there may be pathological links between IgG4-related dacryoadenitis and Castleman disease.
本研究的目的是报告一例先前诊断为Castleman病的患者出现慢性硬化性泪腺炎且IgG4水平升高的病例。一名79岁男性注意到左下颔肿胀,最初是在8年前发现的。通过对下颌下腺活检的组织病理学检查,他被诊断为Castleman病。从那时起,腺体大小未变,且他没有全身炎症体征或症状。一年前他出现复视,CT扫描显示双侧泪腺肿胀。他被转诊至我院进行进一步检查。该患者接受了部分泪腺切除术。通过组织病理学检查,他被诊断为血清IgG4水平升高的慢性硬化性泪腺炎。他接受了口服类固醇治疗,肿胀的泪腺明显改善。结果表明,IgG4相关性泪腺炎与Castleman病之间可能存在病理联系。