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Publikováno v:
Oxford Medical Case Reports
Immunoglobulin A (IgA) vasculitis is characterized by small vessel vasculitis involving immune complexes and IgA deposition. The development of heparin-induced thrombocytopenia (HIT) during IgA vasculitis is extremely rare. An 87-year-old man present
Autor:
Firas Hussein, Zainab Omar
Publikováno v:
Oxford Medical Case Reports
Dyskeratosis congenita (DC) is an inherited disease characterized by the triad of abnormal skin pigmentation, nail dystrophy and mucosal leukoplakia. Non-cutaneous abnormalities (dental, gastrointestinal, genitourinary, neurological, ophthalmic, pulm
Autor:
Priyanka T Bhattacharya, Mathew S. Maurer, Jan M. Griffin, Alyson N. Fox, Charles C. Marboe, Monica P. Goldklang, Jeanine D'Armiento, Andrew Eisenberger, Helen Remotti, Stephen M. Lagana
Publikováno v:
Oxford Medical Case Reports
Wild-type ATTR cardiac amyloidosis (ATTRwt-CA) is not as rare as previously thought to be. Patients with infiltrative cardiac amyloidosis often present with right-sided heart failure (HF) symptomatology. Clinically significant liver disease and cirrh
Autor:
Osman K. Yousafzai, Muhammad Umer, Riley G Jones, Muhammad Omer Zaman, Bernard Kim, Roshan Shah, Kevin Kim
Publikováno v:
Oxford Medical Case Reports
Polycythemia vera is a rare hematological disorder that can cause heart failure with reduced ejection fraction from chronic micro-vascular ischemia. Appropriately recognizing the underlying cause of cardiomyopathy is essential to decrease morbidity a
Autor:
Sadettin Uslu
Publikováno v:
Oxford Medical Case Reports
Autor:
Kazutetsu Aoshiba, Yukihisa Takeda, Hayato Kinoshita, Mariko Ono, Hiroyuki Nakamura, Yoko Nagatomo
Publikováno v:
Oxford Medical Case Reports
Acute respiratory illnesses that presented with diffuse ground-glass opacities (GGOs) on chest computed tomography (CT) scan suggest the diagnosis of coronavirus disease 2019 (COVID-19). However, many other diseases show similar CT findings, which of
Publikováno v:
Oxford Medical Case Reports
Diabetic ketoacidosis (DKA) is considered as a serious complication of type 1 diabetes mellitus in pediatrics. Severe dyslipidemia in DKA is a rare eventuality. We report on a 10-year-old female presented with severe DKA. The serum was lipemic with s
Publikováno v:
Oxford Medical Case Reports
A hepatobronchial fistula (HBF) is a rare condition, defined as an abnormal connection of the respiratory system with the liver parenchyma. Although imaging may be helpful for diagnosis, fistulae are often difficult to identify. An 81-year-old woman
Publikováno v:
Oxford Medical Case Reports
A 78-year-old, overweight woman with a severe individual history of the cardiovascular system was admitted in the intensive care unit with acute pulmonary edema. Despite appropriate emergency treatment, the patient did not show any clinical improveme
Publikováno v:
Oxford Medical Case Reports
Laron syndrome (LS) is a rare autosomal recessive disorder characterized by dwarfism and typical facial phenotype. This report is the first to present three cases of Laron syndrome affecting three female siblings from Syria. The index case presented