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41 Possible Causes for Malaise, Raynaud Phenomenon, Splinter Hemorrhage

  • Hypereosinophilic Syndrome

    Splinter hemorrhages were found in both hands.[] phenomenon The skin is among the most common organ systems involved in hypereosinophilic syndrome; more than half of all patients have cutaneous involvement.[] Six months after the onset of symptomatology there were generalized malaise, uncontrolled fever, gingival haemorrhage, asthenia and adynamia; a blood cell count reported blasts[]

  • Arterial Embolism

    Can also get microangiopathic hemolytic anemias like TTP/HUS, HELLP, and in Catastrophic APS (see below) Skin manifestations are common and include splinter hemorrhages, livedo[] phenomenon H01629 慢性動脈閉塞症 治療薬 ベラプロストナトリウム [DR: D01551 ] アルガトロバン水和物 [DR: D00181 ] アルプロスタジル [DR: D00180 ] アルプロスタジル アルファデクス [DR: D02705 ] チクロピジン塩酸塩 [DR: D01028 ] シロスタゾール [DR[] […] occlusive disease BD40 Atherosclerotic chronic arterial occlusive disease H01629 慢性動脈閉塞症 BD41 Non-atherosclerotic chronic arterial occlusive disease H01629 慢性動脈閉塞症 BD42 Raynaud[]

  • Systemic Lupus Erythematosus

    phenomenon, pulmonary, hematological, gastrointestinal, ocular.[] In addition, individuals also experience fever, fatigue, malaise, sensitivity to light and development of butterfly shaped rashes.[] phenomenon) Shortness of breath Chest pain Dry eyes Easy bruising Anxiety Depression Memory loss[]

  • Rheumatoid Arthritis

    Phenomenon Reactive Arthritis Rheumatoid Arthritis S Scleroderma Sjögren's Syndrome Spinal Stenosis Spondyloarthritis Systemic Lupus Erythematosus (Juvenile) T Takayasu's[] A 66-year-old man with seronegative, erosive rheumatoid arthritis for 12 years presented with malaise, elevated alkaline phosphatase and gamma-glutamyl transferase, and leg[] During the early stages of RA, you may feel a variety of symptoms, including: general weakness or a feeling of malaise dry mouth dry, itchy, or inflamed eyes eye discharge[]

  • Granulomatosis with Polyangiitis

    The tips of his fingers were cyanotic because of ischemia, and his fingernails manifested multiple splinter hemorrhages.[] phenomenon (white/purple fingers on exposure to the cold) is rare.[] […] considered when patients do not improve despite adequate treatment of otologic symptoms, when patients have unspecific symptoms suggesting systemic disease (e.g. fever, malaise[]

  • Microscopic Polyangiitis

    Cutaneous lesions (purpura, splinter hemorrhages) are found in 44 to 58% of the patients.[] Other systemic manifestations include cutaneous involvement (eg, subcutaneous nodules), purpura or Raynaud phenomenon, coronary arteritis, pericarditis, and hematologic abnormalities[] History Constitutional manifestations of microscopic polyangiitis (MPA) include the following: Fever (55%) Malaise, fatigue, flulike syndrome Myalgia (48%) Weight loss (72%[]

  • Muckle Wells Syndrome

    Abstract Muckle-Wells syndrome (MWS) is a rare syndrome, characterized by chronic recurrent urticaria, often combined with fever, chills, rigors, malaise, and arthralgia.[] ) Osler nodes (TENDER raised lesions on fingers/toepads) Murmur Janeway lesions (microembolus -- small PAINLESS erythematous lesions on palm/sole) Anemia Nail bed splinter[] Intense general malaise and chills occur at the same time and lead to severe disability.[]

  • Cutaneous Leukocytoclastic Vasculitis

    No splinter hemorrhages, jaundice, lymphadenopathy, heart murmur, pericardial rub, or joint inflammation were noted on physical exam.[] B-cell lymphoproliferative disorders (multiple myeloma, Waldenstrom macroglobulinemia), clinically characterized by manifestations of gangrene, ulcers, acrocyanosis and Raynaud’s[] Over the past 3 to 4 weeks, he has had malaise, nonproductive cough, and a decline in mental status but no fever, headache, nausea, light-headedness, hemoptysis, or melena[]

  • Livedo Reticularis

    A 38-year-old woman presented with fever, malaise, arthritis and livedo reticularis in a severe form. Antibodies to native DNA and an increased level of aCL were found.[] hemorrhages, and anetoderma.[] A 31-year-old woman with MS developed livedo reticularis and secondary Raynaud phenomenon 2.5 years after introduction of interferon beta-1b.[]

  • Cryoglobulinemia

    […] myocardial infarction) disturbances; vasculitis-driven intestinal ischemia, intestinal perforation, cholecystitis, or pancreatitis, causing acute abdominal pain, general malaise[] Diagnosis Pathology: dermal leukocytoclastic vasculitis - perivascular polymorphonuclear infiltration with tissue extravasation and fragmentation in the dermis Clinical Splinter[] Most common clinical manifestations in CryoVas are skin lesions (orthostatic purpura and ulcers), weakness, peripheral neuropathy, Raynaud's phenomenon, sicca syndrome, membranoproliferative[]

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