BCG-Related Immune Reconstitution Inflammatory Syndrome and Delayed Donor Chimerism After Allogeneic HSCT in T-B-NK+ SCID: A Successful Report of Steroid-Sparing Management [0.03%]
T-B-NK+重症联合免疫缺陷患者异基因HSCT后类BCG-相关免疫重建炎症综合征及供者嵌合体延迟的一项成功病例报道
Seyed Reza Abdipour Mehrian,Sarah Ravankhah,Kiarash Kavari et al.
Seyed Reza Abdipour Mehrian et al.
Background: Severe combined immunodeficiency (SCID) is a life-threatening disorder that requires early hematopoietic stem cell transplantation (HSCT). In regions where Bacillus Calmette-Guérin (BCG) vaccination is routin...
Granulomatosis With Polyangiitis Presenting as Pulmonary Nodules: A Case Study and Literature Review [0.03%]
多血管炎以肺结节形式表现的肉芽肿病一例及文献复习
Yanghang Chen,Haihong Zheng,Liuyang Gong
Yanghang Chen
This article presents a case of myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA)-positive granulomatosis with polyangiitis (GPA) presenting initially as chronic cough. Pulmonary shadows persisted and progressed despite antibio...
Not All That Itches Is DRESS: A Case Report of Lichenified Dermatosis and Hypereosinophilia Associated With Tocilizumab [0.03%]
并非所有瘙痒都是DRESS（药物反应伴嗜酸粒细胞增多和淋巴结肿大综合症）：托珠单抗相关lichenified皮肤病和淋巴细胞增多的病例报告
Mani Maheshwari,Brian Swick,Benjamin Davis et al.
Mani Maheshwari et al.
Drug-induced hypereosinophilic syndromes (HESs) have been associated with a variety of medications, including biologic agents. We present a case of an 85-year-old female with a history of giant cell arteritis (GCA) complicated by ascending ...
Diagnosing Hyper IgE Syndrome in a Resource-Limited Setting: A Case Report Highlighting the Utility of Clinical Scoring and Multidisciplinary Management [0.03%]
资源有限条件下的低免疫球蛋白E综合征的诊断：一个病例报告强调了临床评分和多学科管理的作用
Roshna Devi,Huda Raja,Prithvi Raj et al.
Roshna Devi et al.
Background: Hyperimmunoglobulin E syndrome (HIES), also known as Job's syndrome, is an uncommon primary immunodeficiency disorder characterized by markedly elevated serum IgE levels, recurrent infections, both bacterial a...
A Novel MYO5A Mutation (c.3508C>T) in a 27-Month-Old Girl With Hypotonia and Developmental Delay: Expanding the Phenotypic Spectrum of Griscelli Syndrome Type 1 [0.03%]
MYO5A新突变(c.3508C>T)一例：两名27个月发育迟缓女婴及其Griscelli综合征1型的临床表型拓展
Davoud AmirKashani,Soudabeh Hosseini,Marziyeh Mojbafan et al.
Davoud AmirKashani et al.
Background: Griscelli syndrome (GS) is a rare autosomal recessive disorder, characterized by pigmentary dilution of hair and skin. There are three known types of this disease. GS type 1 (GS1), due to mutations in MYO5A, i...
Supplemental Bee Pollen Ingestion With Resultant Anaphylaxis and Allergic Asthma: Case Report [0.03%]
关于花粉摄入引起过敏性哮喘和全身过敏反应的病例报告
Erin Eickholt,Victoria Norelli,Kathleen Martin et al.
Erin Eickholt et al.
Bee pollen has become an increasingly popular dietary supplement due to potential therapeutic effects. However, ingestion has been shown to trigger allergic responses as severe as anaphylaxis. This case highlights allergic asthma developmen...
Lucía Ferrer Clavería,Verónica Perciun,María Teresa Sobrevía Elfau et al.
Lucía Ferrer Clavería et al.
Dragon fruit, also known as pitahaya, has become increasingly popular in Europe and the United States owing to its nutritional value and potential health-promoting properties. This study describes a patient with anaphylaxis after the ingest...
A Novel Variant of CORO1A Gene Contributing to the Development of Primary Immunodeficiency in Children [0.03%]
CORO1A基因新突变导致儿童原发性免疫缺陷病
Alanoud Aljohani,Yazeed Alayed,Bashayer Alrasheed et al.
Alanoud Aljohani et al.
Introduction: The case report describes a novel finding of a homozygous variant in the coronin 1A (CORO1A) gene, associated with atypical severe combined immunodeficiency (SCID) in a 9-year-old female patient with recurre...
Acute Motor Axonal Neuropathy Coexisting With Ankylosing Spondylitis: A Case-Based Review [0.03%]
与强直性脊柱炎共存的急性运动轴突神经病：基于病例的回顾
Yiğit Can Güldiken,Batool Achmar,Sema Kaymaz Tahra
Yiğit Can Güldiken
Guillain-Barré syndrome (GBS) is a rare autoimmune disorder characterized by peripheral nerve involvement. Among the many kinds of GBS, acute motor axonal neuropathy (AMAN) syndrome has been shown to have distinct clinical characteristics ...
Homozygous C1qA Deficiency Presenting as Early-Onset Systemic Lupus Erythematosus: A Case Report With a Literature Review [0.03%]
C1qA纯合子缺乏导致早期系统性红斑狼疮一例及文献复习
Hadi Mottaghipisheh,Andisheh Mosaffa Jahromi,Fatemeh Mirzaei et al.
Hadi Mottaghipisheh et al.
Background: Childhood-onset systemic lupus erythematosus (cSLE) can be particularly severe when associated with inborn errors of immunity. Hereditary C1q deficiency is an exceptionally rare complement disorder that confer...