A case of steroid-induced mania following lamotrigine-induced drug reaction with eosinophilia and systemic symptoms (DRESS): a cautionary tale [0.03%]
一例拉莫三嗪诱导的药物反应伴嗜酸性粒细胞增多和系统症状(DRESS)继发糖皮质激素所致躁狂症的病例报告：一则警示故事
Bianca Te,Edwin Tam,Sheila Au
Bianca Te
Drug reaction with eosinophilia and systemic symptoms is a severe cutaneous adverse reaction frequently associated with lamotrigine, an antiepileptic drug also used to treat bipolar disorder. Although a mainstay of therapy for drug reaction...
Case report: Challenging diagnosis of leukocytoclastic vasculitis, caused by recurrent urinary tract infection [0.03%]
病例报告：由反复泌尿系感染引起的白细胞破裂性血管炎的疑难诊断
Slavena Dineva,Christoph Henzen,Thomas Hodel et al.
Slavena Dineva et al.
We present a 63-year-old male with a history of chronic cystoprostatitis and urethral stricture with recurrent purpuric skin lesions and fulminant uroseptic shock. Initial treatment for suspected septic vasculitis with antibiotics and corti...
Diagnostic challenges and perioperative management of a lateral cystic neck mass in an adult patient with hemophilia B: A case report [0.03%]
成人B型血友病患者的侧向囊性颈部肿块的诊断挑战及围手术期管理：病例报告
William G Ruley,Wesley A Greene,Daniel A Cranfield et al.
William G Ruley et al.
Lymphatic malformations and branchial cleft anomalies are rare congenital lesions that can present similarly as cystic neck masses, often in childhood, but occasionally in adults. Differentiating between the two can be challenging, especial...
Kayla J Steinberger,John C Goellner,Hillary E Morley
Kayla J Steinberger
A 21-month-old male presented with a suction blister on his thumb caused by the thumb being caught in a pacifier overnight. This rare presentation highlights the need for careful monitoring of pacifier use in young children to prevent simil...
Heterozygous X-linked Alport syndrome in a pregnant woman: A case report [0.03%]
杂合子X连锁Alport综合征并发妊娠1例报告
Caroline Gee,Matthew D Nguyen,Dao Le et al.
Caroline Gee et al.
Alport syndrome is a genetic disorder of chronic kidney disease, hearing loss, and ocular abnormalities, caused by mutations in type IV collagen. While X-linked Alport Syndrome demonstrates characteristic severe renal failure in males, it h...
Infantile hypertrophic cardiomyopathy masquerading as cardiac tamponade: A case report [0.03%]
以心包填塞样表现为首发的肥厚型心肌病一例报告
Theresia Sri Rezeki Sembiring,Mochamad Faisal Adam
Theresia Sri Rezeki Sembiring
Hypertrophic cardiomyopathy in infancy often follows a rapidly progressive clinical course, with many cases becoming fulminant and fatal. We reported a case of a 4-month-old infant with worsening breathlessness. While admitted, she was in s...
Quynh Kieu,Brianna Leyden
Quynh Kieu
Kikuchi-Fujimoto disease (KFD) is a rare, benign, self-limited lymphadenitis most commonly affecting children and young adults, particularly females of Asian descent. Its etiology is unclear but is thought to involve immune dysregulation tr...
Persistent eosinophilia following treatment for pediatric pyogenic liver abscess: A case report [0.03%]
一例儿童肝脏脓肿治疗后持续嗜酸细胞增多症的病例报告
Alex F Gimeno,Walter Dehority,Stephanie L Rolsma et al.
Alex F Gimeno et al.
This case report describes a case of pyogenic liver abscess potentially associated with toxocariasis, a rare disease in the United States. A 3-year-old girl presented with new abdominal pain and fever. Contrasted computed tomography of the ...
Purification and antibody-free ex-vivo expansion of peripheral blood-derived autologous natural killer cells: A Malaysian case series on patient safety and tolerability [0.03%]
基于外周血的同种异体天然杀伤细胞的纯化和无抗体体外扩增：马来西亚患者的案例系列研究——有关安全性和耐受性的分析
Ramesh Thevendran,Manickam Ravichandran,Seng Kong Tham
Ramesh Thevendran
Natural killer cells are the most researched and employed cells for immunotherapy, which have expanded from autologous immune-enhanced therapies to genetically enhanced cell therapies such as chimeric antigen receptors natural killer cells....
Secondary hemophagocytic lymphohistiocytosis following blood transfusion in the absence of an identifiable trigger [0.03%]
无明确诱因输血后继发性噬血细胞综合征一例报告
Ashley M Tuin,Kyle Gilkeson,Joseph Thirumalareddy
Ashley M Tuin
Hemophagocytic lymphohistiocytosis is a life-threatening inflammatory syndrome resulting from uncontrolled immune activation. Secondary hemophagocytic lymphohistiocytosis is typically triggered by infection, malignancy, or autoimmune diseas...