The paradox of hypothyroidism: elevated cardiac biomarkers without coronary artery disease [0.03%]
甲状腺功能减退的悖论：无冠状动脉疾病但心脏生物标志物升高
Pooja Alipuria,Atush Alipuria
Pooja Alipuria
Summary: This case report describes a 55-year-old male with hypothyroidism who presented with chest pain, elevated cardiac biomarkers (creatine kinase-MB (CK-MB) and troponin T), and abnormal electrocardiogram (ECG), find...
Intravascular large B-cell lymphoma presenting with SIAD and pituitary insufficiency: a unifying diagnosis for multiple endocrinopathies [0.03%]
以SIAD和垂体功能不全为表现的血管内大B细胞淋巴瘤：多种内分泌疾病的统一诊断
Zoe Gavey,Raymond Dharmaputra,Nirjhar Nandi et al.
Zoe Gavey et al.
Summary: Intravascular large B-cell lymphoma is an uncommon haematological condition that may present with a variety of non-specific symptoms and signs. In this report, we discuss the case of a man in his 70s who presente...
Co-existing phaeochromocytoma and anti-HMG-CoA reductase immune-mediated necrotising myositis: a diagnostic challenge [0.03%]
伴抗3-羟基-3-甲基-glutaryl-coenzyme a 还原酶免疫介导性坏死性肌炎的嗜铬细胞瘤的诊断难题：一例报道及文献回顾
Sean Maher,Eibhlin Lonergan,Sarah Fullam et al.
Sean Maher et al.
Summary: We report the case of a 62-year-old male who developed progressive lower limb and bulbar muscle weakness associated with elevated creatine kinase (CK) levels on a background of statin use following myocardial inf...
Luis Miguel Osorio-Toro,Yessica Alejandra Ordoñez-Guzman,Jhon Herney Quintana-Ospina et al.
Luis Miguel Osorio-Toro et al.
Summary: Thyroid storm, also known as thyroid crisis, is a serious medical condition that occurs when there is an extreme overproduction of thyroid hormones. It usually develops in individuals with uncontrolled hyperthyro...
Does X mark the spot? A case series of discrepant preoperative insulinoma localization [0.03%]
X型定位吗？术前胰岛素瘤定位不一致的病例系列分析
Shouheng Goh,Oana-Patricia Zaharia,Emily Reutemann et al.
Shouheng Goh et al.
Summary: We explored the challenges associated with the localization of insulinomas, pancreatic neuroendocrine tumors responsible for hypoglycemia. Insulinomas often present with varied symptoms, leading to potential diag...
Concordant X-linked hypophosphatemic rickets in monozygotic twins: diagnostic challenges and a novel genetic insight [0.03%]
单卵双生子同患X染色体连锁低磷血症性佝偻病的诊断挑战及新的基因研究发现
Sara Ribeiro,Telma Moreno,Ana Varela et al.
Sara Ribeiro et al.
Summary: X-linked hypophosphatemic (XLH) is the most common inherited form of rickets, caused by inactivating mutations in the PHEX gene. Resultant overproduction of fibroblast growth factor 23 (FGF23) leads to renal phos...
Acute hepatitis induced by insulin overdose and oral glucose administration in a child managed under a hybrid continuous care model [0.03%]
混合连续照顾模式下儿童因胰岛素过量和口服葡萄糖诱发的急性肝炎病例报告
Judy Kattan,Kowshik Gupta,Hala Zakaria et al.
Judy Kattan et al.
Summary: Acute hepatitis was reported in a 10-year-old male patient with type 1 diabetes, believed to be due to hepatic glycogenosis from insulin overdose and oral glucose administration. Liver function abnormalities, inc...
Severe lumbosacral polyradiculopathy secondary to micronutrient deficiencies in a patient on semaglutide therapy following bariatric surgery [0.03%]
微营养素缺乏继发司美格鲁肽治疗的代谢手术患者严重腰骶多神经根病一例
Emma C Donigan,Elizabeth Ingersent,Erik J Wanberg et al.
Emma C Donigan et al.
Summary: Bariatric surgery and glucagon-like peptide-1 receptor agonist medications (GLP-1RAs) are common and effective methods for treating obesity. Since bariatric surgery is associated with an increased risk of malnutr...
Retroperitoneal bronchogenic cyst masquerading as an adrenal incidentaloma [0.03%]
以肾上腺意外瘤为表现的腹膜后支气管源性囊肿病例报告
Trevor Tam,Nishani Jayatunge,Louis Saada et al.
Trevor Tam et al.
Summary: Bronchogenic cysts, developmental malformations of the primitive foregut, extremely rarely occur in the retroperitoneum. Here, we present a retroperitoneal bronchogenic cyst presenting as an adrenal incidentaloma...
Combined alkaptonuria and osteoporosis contributing to chronic back pain [0.03%]
黑尿酸病合并骨质疏松导致慢性背痛病例报告
Anna Riegler,Gurpreet Anand
Anna Riegler
Summary: Alkaptonuria is a rare autosomal recessive metabolic disorder caused by a deficiency in homogentisate 1,2-dioxygenase (HGD), leading to the accumulation of homogentisic acid (HGA) in connective tissues, cartilage...