Hypophysitis Secondary to Small Vessel ANCA Vasculitis Treated With Rituximab

被引:1
作者
Kumar, Nankee K. [1 ]
Rivadeneira, Ana [2 ]
Banerjee, Shubhasree [3 ]
Gubbiotti, Maria [4 ]
Yoshor, Daniel [1 ]
Jackson, Christina [1 ]
Kharlip, Julia [5 ]
White, Caitlin A. [5 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Neurosurg, 3400 Civ Ctr Blvd, Philadelphia, PA 19104 USA
[2] Thomas Jefferson Univ, Div Endocrinol, Philadelphia, PA USA
[3] Univ Penn, Div Rheumatol, Perelman Sch Med, Philadelphia, PA USA
[4] UNiv Texas MD Anderson Canc Ctr, Div Pathol, Houston, TX USA
[5] Univ Penn, Perelman Sch Med, Div Endocrinol Diabet & Metab, Philadelphia, PA USA
关键词
hypophysitis; ANCA associated vasculitis; rituximab; GRANULOMATOSIS; POLYANGIITIS; CYCLOPHOSPHAMIDE;
D O I
10.1016/j.aace.2023.12.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Objective: Antineutrophil cytoplasmic antibody (ANCA) associated vasculitis is a rare small vessel vasculitis that can cause pituitary hypophysitis. Hypophysitis is difficult to treat, often requiring high doses of glucocorticoids with frequent flaring as glucocorticoids are tapered. We present a case of ANCA vasculitis involving the pituitary gland successfully treated with rituximab. Case Report: Fifty-one-year-old woman developed progressive frontal headaches, congestion, and epistaxis. Sinus computed tomography scan showed pituitary enlargement and chronic mucosal disease. Pituitary magnetic resonance imaging (MRI) confirmed a diffusely enlarged pituitary with a thickened pituitary stalk. Serologic evaluation revealed elevated inflammatory markers, positive perinuclear ANCA (p-ANCA), and an elevated serum anti-proteinase 3 (anti-PR3) antibody. The patient underwent pituitary biopsy, which showed adenohypophysitis with dense lymphoplasmacytic infiltration, some arranged perivascularly, compatible with involvement of the pituitary gland by ANCA vasculitis. The patient began rituximab and reported resolution of daily headaches, congestion, and epistaxis. Pituitary MRI scan 6 months after rituximab showed reduction in pituitary gland size and stalk thickening. Discussion: ANCA vasculitis is a rare etiology of pituitary hypophysitis, which can present a diagnostic and therapeutic challenge. Pituitary involvement of ANCA vasculitis can be identified through pANCA or cytoplasmic ANCA (c-ANCA) and biopsy of the involved tissue. Rituximab, a monoclonal antibody against CD20, has been successfully used to treat ANCA vasculitis and in this case, led to clinical improvements and reduction in the size of the pituitary gland. Conclusion: Pituitary biopsy enabled confirmation of ANCA hypophysitis and facilitated treatment with a steroid-sparing agent. (c) 2024 AACE. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:55 / 59
页数:5
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