台耳醫誌

雜誌專區 -第57卷第2期

病例報告 
IgG4-Associated Sialadenitis Presenting as a Submandibular Gland Neoplasm—Case Report    僅供有效會員 登入會員查看全文
155~160 
英文 
chronic sclerosing sialadenitis、IgG4-associated sialadenitis、Kuttner’s tumor、submandibular gland neoplasm 
Yih-Min Chu1 、Chien-Han Yuan1,2,3 、Chia-An Hsu1 、Hsin-Ho Chen4 、Ben-Chih Yuan5  
Kaohsiung Armed Forces General Hospital, KaohsiungDepartment of Otolaryngology1 、National Sun Yat-Sen University, KaohsiungInstitute of Medical Science and Technology2 、National Defense Medical Center, TaipeiDepartment of Otolaryngology3 、Fooyin University Hospital, PingtungDepartment of Pathology4 、Fooyin University Hospital, Pingtung, TAIWANDepartment of Otorhinolaryngology5  
A 76-year-old man was seen in the clinic for a painless mass in his left upper neck. Physical examination and computed tomography showed an enlargement of the left submandibular gland. Sonography revealed multiple lobulated hypoechoic lesions within the enlarged left submandibular gland. Excision of the left submandibular gland was performed smoothly. The specimen showed interlobular fibrosis and atrophic acini. There was lymphoplasmacytic infiltration, which had increased immunoglobulin G4 (IgG4) positive plasma cell populations in the gland. The patient’s serum IgG4 was 189 mg/dL, far beyond the reference level of 8-140 mg/dL. These findings were all consistent with IgG4-associated sialadenitis. The man did not receive systemic steroid therapy after the surgery. No disease recurrence was observed in the following year after excision. Though IgG4-associated sialadenitis is usually highly sensitive to steroids, the diagnosis is often made after surgical resection, which is usually also curative. Systemic corticosteroid therapy could be reserved for use in cases of refractory or recurrent diseases. (J Taiwan Otolaryngol Head Neck Surg 2022; 57:155-160)