Results 101 to 110 of about 8,573 (198)
A 51‐year‐old female presenting with headache and vision loss
Headache: The Journal of Head and Face Pain, EarlyView.
Laurel Ovrom +3 more
wiley +1 more source
Could Fabry Disease Cause Giant Coronary Aneurysms in a 7‐Month‐Old Infant: A Case Report
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Fabry disease is a rare X‐linked lysosomal storage disorder that can affect multiple organs. Cardiac involvement, one of its significant manifestations, can begin in childhood and is more prevalent in males, with severity increasing with age and disease progression.
Reza Shabanian +5 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT A 12‐year‐old boy presented with recurrent oral and scrotal ulcers, papulopustular lesions, arthralgia, and a positive pathergy test. Autoimmune tests were negative; ophthalmologic and gastrointestinal assessments were reassuring. Topical therapy and colchicine produced sustained improvement.
Fares Basel Abu Taha +8 more
wiley +1 more source
What Is Your Diagnosis? Blood Smear From a North American Beaver (Castor canadensis)
Veterinary Clinical Pathology, EarlyView.
Lilani Munasinghe +4 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT BCG scar reactivation is classically associated with Kawasaki disease but may also occur during immune activation caused by infections. We report a 26‐month‐old boy with laboratory‐confirmed influenza B who developed transient erythema and swelling at a previous BCG vaccination scar without clinical features of Kawasaki disease or MIS‐C.
Dilara Canbay Özdemir, Oğuzhan Alp
wiley +1 more source
Case Reports in Neurological Medicine, 2016 This case report describes a 41-year-old previously healthy male who presented with stuttering transient ischemic symptoms and radiographic evidence of a left common carotid artery thrombus as well as acute and subacute ischemic infarcts in the left ...
David Roshal
doaj +1 more source
Immunophenotypic characteristics of plasma cells in POEMS syndrome
Cytometry Part B: Clinical Cytometry, Volume 110, Issue 4, Page 266-273, July 2026.Abstract To analyze the immunophenotypic characteristics of plasma cells in patients with polyneuropathy, organomegaly, endocrinopathy, myeloma protein, and skin changes (POEMS) syndrome. This retrospective study included patients with POEMS syndrome hospitalized in the Department of Hematology, Huashan Hospital, from September 2017 to August 2025 ...
Zhenhua Wang +6 more
wiley +1 more source
An unusual case of extreme thrombocytosis caused by iron deficiency
, 2020 Iron deficiency is a common cause of reactive thrombocytosis resulting in usually mild to moderately increased but sometimes even in extreme thrombocytosis (ie, >1000×109/L).
Bergmann, Kristin, Bergmann, Olav J.
core +1 more source
JIMD Reports, Volume 67, Issue 4, July 2026.ABSTRACT Biallelic pathogenic variants in PNPT1 cause combined oxidative phosphorylation deficiency 13 (COXPD13) (MIM #614932), linking mitochondrial dysfunction to type I interferon (IFN) activation through cytosolic leakage of mitochondrial double‐stranded RNA (mt‐dsRNA).
Dan Ross Brooks +15 more
wiley +1 more source
Respirology Case Reports, Volume 14, Issue 7, July 2026.Multisystem IgG4‐RD can closely mimic metastatic malignancy and should be considered when thoracic and extrapulmonary mass‐forming lesions coexist. Timely biopsy confirmation is essential to avoid misdiagnosis and treatment delay. ABSTRACT IgG4‐related disease (IgG4‐RD) is a multisystem fibroinflammatory condition that can mimic metastatic malignancy ...
Ho Young Lee, Juyeon Kang
wiley +1 more source