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1,296 Possible Causes for Splenomegaly, Vasculitis

  • Gastrointestinal Hemorrhage

    This is often due to pre-existing liver disease and splenomegaly.[] We describe a case of systemic Candida albicans infection associated with life-threatening gastrointestinal hemorrhage due to unusual necrotizing vasculitis involving the[] Other signs to look for are ascites and erythema (chronic liver disease) and splenomegaly and dilated abdominal wall veins (portal hypertension).[]

  • Rheumatoid Arthritis

    It is extremely rare for RA to present as FS or develop after initially presenting as neutropaenia and splenomegaly.[] Extensive investigations did not reveal evidences of other systemic causes such as malignancy or systemic vasculitis.[] Other: thyroid disorders, osteoporosis, depression, splenomegaly.[]

  • Felty's Syndrome

    Computed tomography of the pelvis led to an incorrect diagnosis of malignancy, while radionuclide imaging using Tc-99m sulfur colloid confirmed the diagnosis of ectopic splenomegaly[] We address the issue of "adding fuel to the fire" and review reported implications of GCSF in induction of vasculitis.[] Abstract The syndrome of atrophic polyarthritis occurring in an adult, associated with fever, secondary anemia, leukopenia and splenomegaly, was described by Felty 1 in 1924[]

  • Pulmonary Lymphomatoid Granulomatosis

    A computerized tomography (CT) scan demonstrated bilateral pulmonary nodules and splenomegaly.[] Vasculitis is so complex as to con two giants in the field, Drs. Averill Liebow and Herbert tinue to warrant a separate chapter. Spencer.[] The child redeveloped splenomegaly and fever, and then suffered an acute decompensation with hypoxemia, tachypnea, splenomegaly, and cardiac gallop.[]

  • Lupus Erythematosus

    […] keratoconjunctivitis sicca as well as more uncommon manifestations Haematologic manifestations, including cytopenias, thrombophilia, thromboembolic disease, lymphadenopathy and splenomegaly[] Vasculitis : small vessel vasculitis , urticarial vasculitis and less often, vasculitis of medium and large vessels Livedo reticularis and antiphospholipid syndrome Chilblain[] Enlargement of the spleen (splenomegaly) occurs in about 10% of people.[]

  • Systemic Lupus Erythematosus

    […] relapsing illness, with a variety of different presentations. [ 5 , 6 ] Symptoms and signs are often nonspecific - eg, fatigue (can be severe and debilitating), malaise, fever, splenomegaly[] Classification and diagnostic criteria in systemic vasculitis. Best Pract Res Clin Rheumatol. 2005;19:209–221. Ramos-CasalsM, Nardi N, LagruttaM, et al.[] […] relapsing illness, with a variety of different presentations. [ 5, 6 ] Symptoms and signs are often nonspecific - eg, fatigue (can be severe and debilitating), malaise, fever, splenomegaly[]

  • Subacute Bacterial Endocarditis

    Fever, anaemia, splenomegaly and positive blood cultures for Gram-negative bacteria were found on admission.[] Findings compatible with both SBE and marantic endocarditis due to a B-cell lymphoproliferative disorder included an elevated ESR, and splenomegaly.[] Splenomegaly and clubbing of fingers and toes may occur because of prolonged infection.[]

  • Sarcoidosis

    In this report, we describe the case of a 12-year-old girl presenting with fatigue and weight loss, with a painless hepato-splenomegaly without additional clinical signs on[] Five years ago, Sarcoidosis Vasculitis and Diffuse Lung Diseses, started its publication online -in addition to print - with a renewed Editorial Committee comprised of R.[] Abdomen Check for hepatomegaly and splenomegaly.[]

  • Adult-Onset Still Disease

    […] clinically by high spiking fever, polyarthralgia/arthritis, a salmon-pink evanescent rash, predominantly neutrophilic leucocytosis, lymphadenopathy, liver dysfunction, and splenomegaly[] vasculitis drug-induced vasculitis paraneoplastic vasculitis Petechiae as a manifestation of leukocytoclastic vasculitis secondary to Listeria bacteremia Case Rep Infect[] Arthritis (OR, 8.6; 95% confidence interval [CI], 1.5-49.1; p 0.014), pharyngitis (OR, 6.9; 95% CI, 1.5-30.2; p 0.010), splenomegaly (OR, 5.4; 95% CI, 1.1-26.7; p 0.039),[]

  • Familial Mediterranean Fever

    Her persistent left elbow effusion resolved and her splenomegaly rapidly disappeared.[] An association of FMF with systemic vasculitis, namely Henoch-Schönlein purpura, polyarteritis nodosa and Behçet's disease has been described.[] Cutaneous necrotizing vasculitis repeatedly emerging with febrile attacks should be included among the skin manifestations of FMF.[]

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