Majlinda Xhikola,Aditya S Shirali,George A Sarosi et al.
Majlinda Xhikola et al.
Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors that secrete catecholamines. While classic symptoms such as palpitations, sweating, and headaches may occur, many patients exhibit nonspecific or mild signs due to ...
Antiphospholipid Syndrome-Associated Lemierre's Syndrome With Extensive Cervicothoracic Venous Thrombosis Mimicking Thoracic Outlet Syndrome [0.03%]
Neha Arsha,John Zadran,Abhimannu Majumder et al.
Neha Arsha et al.
Lemierre's syndrome is a rare postanginal septic thrombophlebitis involving the internal jugular vein in younger adults. Extension into the thoracic inlet and upper extremity venous system is uncommon, and the role of underlying autoimmune ...
Ruba Habib,Rouba Isshak,Rayan Sabouh et al.
Ruba Habib et al.
Sugammadex is a new drug that gained FDA approval in 2015 for rapid reversal of aminosteroid neuromuscular blockade as it showed faster action than the traditional drugs, neostigmine and is generally well tolerated. However, hypersensitivit...
Functional Recovery Following Intensive Upfront Therapy in Multiple Myeloma Patients With Poor Performance Status: A Case Series [0.03%]
强化诱导治疗后多发性骨髓瘤患者的功能恢复：一系列案例研究
Kareem Latif,Jerry Qi,Pranati Shah et al.
Kareem Latif et al.
Patients with newly diagnosed multiple myeloma (MM) may present with profound functional impairment due to high disease burden, and an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 4 is often viewed as a barrier to in...
Srijani Thannir,Jonathan Kutcher,Jayalekshmi Jayakumar et al.
Srijani Thannir et al.
Vitamin B12 deficiency is classically associated with megaloblastic anemia and neurologic or neuropsychiatric manifestations; however, in rare cases, it may present with pancytopenia and laboratory features that mimic hemolytic anemia. Pern...
Morganella Morganii Respiratory Infection as an Initial Presentation of Acute Myeloid Leukemia With Monocytic Differentiation: A Rare Opportunistic Pathogen in a Newly Diagnosed Immunocompromised Host [0.03%]
肠道沙雷氏菌呼吸道感染作为单核细胞分化急性髓系白血病的初始表现：新诊断的免疫抑制宿主罕见机会致病菌
Varun Muppidi,Ragul Manoharan,Rouba Isshak et al.
Varun Muppidi et al.
Infective manifestations of hematological malignancies can be traced to a variety of pathogens, necessitating broad spectrum empiric antibiotic coverage, and prompt identification of pathogenic microbes to improve clinical outcomes. We pres...
Fungating Mass of the Glans Penis: A Case Report and Discussion on Penile Squamous Cell Carcinoma [0.03%]
阴茎鳞状细胞癌病例报告及讨论：阴茎龟头外生性肿物一例报告与讨论
Dominic M Collins,Alex Marvin Simpkins,John Diks et al.
Dominic M Collins et al.
Penile squamous cell carcinoma (PSCC) is a rare presentation in the United States and Europe, accounting for only 1% of male malignancies. Most commonly due to human papilloma virus (HPV), PSCC has an insidious onset, often ignored by patie...
Primary Intestinal Lymphangiectasia Presenting as Recurrent Chylous Ascites: A Rare Case [0.03%]
初发表现为反复性乳糜性腹水的原发肠道淋巴管扩张症罕见病例报告
Malak Hroub,Basheer Babaa,Abdallah Dwayat et al.
Malak Hroub et al.
Primary intestinal lymphangiectasia (PIL) is a rare protein-losing enteropathy, typically diagnosed in childhood. Adult-onset PIL is exceptionally rare and poses a significant diagnostic challenge, often diagnosed as other gastrointestinal ...
Unusual Thromboembolic Sequelae of MRSA Bacteremia in A Pediatric Patient: A Case Report [0.03%]
儿童MRSA菌血症的罕见栓塞性后遗症一例报告
Shahd Khatib,Omer Innab,Nardeen Hammad et al.
Shahd Khatib et al.
Methicillin-resistant Staphylococcus aureus infection can cause serious illness in children. It can progress to life-threatening bloodstream issues or bone infections, including: deep vein thrombosis, septic pulmonary embolism, toxic shock ...
Expanding the Phenotypic Spectrum of SLC1A4-Related Spastic Tetraplegia: A Case With Novel Multisystem Features [0.03%]
SLC1A4相关性四肢痉挛性瘫痪表型谱的扩展：一例具有新型多系统受累特征的新病例报告
Ramzi H Mujahed,Leyana Alawawdeh,Baraa Nassar et al.
Ramzi H Mujahed et al.
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM) is a rare autosomal recessive neurodevelopmental disorder caused by pathogenic variants in the SLC1A4 gene. 24 cases have been reported worldwide. We describe...