Cerebral toxoplasmosis in a patient with Good's syndrome: A case report and literature review

被引:0
|
作者
Choi, Seoyoung [1 ]
Kwon, Mi Jung [2 ]
Kim, Eun Soo [3 ]
Lee, Heui Seung [4 ]
Jung, Younghee [5 ]
Kim, Joo-Hee [1 ]
Jang, Seung Hun [1 ]
机构
[1] Hallym Univ, Coll Med, Sacred Heart Hosp, Dept Internal Med, Anyang, South Korea
[2] Hallym Univ, Sacred Heart Hosp, Dept Pathol, Coll Med, Anyang, South Korea
[3] Hallym Univ, Sacred Heart Hosp, Dept Radiol, Coll Med, Anyang, South Korea
[4] Hallym Univ, Sacred Heart Hosp, Dept Neurosurg, Coll Med, Anyang, South Korea
[5] Chungnam Natl Univ Hosp, Dept Internal Med, Div Infect Dis, Daejeon, South Korea
来源
ALLERGY ASTHMA & RESPIRATORY DISEASE | 2024年 / 12卷 / 03期
关键词
Cerebral toxoplasmosis; Primary immunodeficiency disease; Thymoma; Cell-mediated immunity; Hypogammaglobu-; linemia; INFECTIONS;
D O I
10.4168/aard.2024.12.3.155
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Good's syndrome is a rare cause of combined B- and T-cell immunodeficiency in adults with a history of thymectomy. The patients with Good's syndrome are susceptible to encapsulated bacterial infections and opportunistic viral/fungal infections. We report a 63-year-old female patient who was diagnosed with cerebral toxoplasmosis in the middle of monthly immunoglobulin treatment for Good's syndrome. She was referred owing to progressive dizziness for one week without any neurologic deficits. Although routine laboratory tests and toxoplasma serology exams were within the normal range, brain image studies suggested cerebral toxoplasmosis, which was confirmed by pathology of brain lesions. She was treated with pyrimethamine and sulfadiazine as well as with systemic corticosteroids, and improved without sequelae. Later, her medication was switched to trimethoprim/sulfamethoxazole as a second-line treatment due to sulfadiazine-related neuropathy. (Allergy Asthma Respir Dis 2024;12:155-159)
引用
收藏
页码:155 / 159
页数:5
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