A case of anti-neutrophil cytoplasmic antibody-associated vasculitis masquerading as Sjogren syndrome

被引:0
|
作者
Pillay, S. Sujitha [1 ]
Nune, Arvind [1 ]
Manzo, Ciro [2 ]
Barman, Bhupen [3 ]
Raza, Hasnain [1 ]
机构
[1] Southport & Ormskirk NHS Trust, Southport PR8 6PN, England
[2] Rheumatol Outpatient Clin, St Agnello, Italy
[3] All India Inst Med Sci AIIMS, Dept Gen Med, Gauhati, India
关键词
anti-neutrophil cytoplasmic antibody; autoimmune disease; case report; Sjogren syndrome; vasculitis; ANCA-ASSOCIATED VASCULITIS; SALIVARY-GLAND INVOLVEMENT; WEGENERS-GRANULOMATOSIS; MORTALITY;
D O I
10.1111/1756-185X.14823
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anti-neutrophil cytoplasmic antibody (ANCA) -positive vasculitis is a small-vessel vasculitis that affects multiple body systems. Salivary gland involvement in ANCA-associated vasculitis is rare. When present, it mimics infection or malignancy, which might lead to misdiagnosis. In this report, we describe a 72-year-old man who presented with parotid and submandibular gland pain and swelling in addition to dry mouth and eyes. He had bilateral non-tender parotid gland lumps and no lymphadenopathies. Laboratory tests were positive for ANCA, hematuria, and proteinuria but negative for Anti-Ro and -La. He was treated with corticosteroids and cyclophosphamide for acute kidney injury. Unfortunately, the patient died a few months later. This case report sheds light on a rare manifestation of salivary gland involvement in ANCA-associated vasculitis that mimics Sjogren syndrome and the challenges associated with its diagnosis and treatment.
引用
收藏
页码:2555 / 2558
页数:4
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