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896 Possible Causes for Purpura, Thrombocytosis

  • Essential Thrombocythemia

    […] hypergammaglobulinemic purpura ( D89.0 ) cryoglobulinemic purpura ( D89.1 ) essential (hemorrhagic) thrombocythemia ( D47.3 ) hemorrhagic thrombocythemia ( D47.3 ) purpura[] The patient was evaluated for thrombocytosis because he was in remission and suffering persistent thrombocytosis under treatment.[] The platelet count may also transiently rise above normal limits with effective treatment for immune thrombocytopenic purpura.36 Following splenectomy for any condition, the[]

  • Systemic Amyloidosis

    Here we described a case who had purpura-like lesions in the initial stage, followed by progressive malfunctions in the kidneys, the heart, the lungs, as well as the liver[] Her past medical history was remarkable for membranoproliferative glomerulonephritis, hypertension, pulmonary hypertension, and anemia of thrombocytosis.[] Oral blood blisters and purpura are rare features of primary systemic amyloidosis (amyloid light-chain (AL) amyloidosis).[]

  • Polyarteritis Nodosa

    We describe the case of a previously healthy 12-year-old boy admitted to a tertiary paediatric centre with the clinical diagnosis of Henoch-Schonlein purpura (HSP).[] Diagnostic Testing: Nonspecific inflammatory markers include elevated ESR or CRP, leukocytosis, anemia of chronic disease, and thrombocytosis.[] The most frequent cutaneous manifestations were ulcers, livedo racemosa, subcutaneous nodules, atrophie blanche lesions and purpuras; with lower limb involvement in all cases[]

  • Meningitis

    […] toxic substances into the circulation and causing fever; if the infection is caused by N. meningitidis , a rash may appear and develop into hemorrhagic spots ( petechiae and purpura[] Minor features include organomegaly, endocrinopathy, characteristic skin changes, papilledema, extravascular volume overload, and thrombocytosis.[]

  • Celiac Disease

    Consider serologic testing for celiac disease with any of following: Addisons disease, amenorrhea, apthous stomatitis, autoimmune myocarditis, chronic thrombocytopenic purpura[] Extreme thrombocytosis as a sign of coeliac disease in the elderly: case report. Eur J Gastroenterol Hepatol 2002 ; 14 : 897 –900. Schafer AI. Thrombocytosis.[] There is some evidence of increased prevalence of celiac disease in people with autoimmune myocarditis, chronic thromboycytopeniac purpura, depression/bipolar disorder, Down[]

  • Appendicitis

    […] inflammatory disease Ruptured ovarian cyst (follicular, corpus luteum) Tubo-ovarian abscess Systemic Diabetic ketoacidosis Porphyria Sickle cell disease Henoch-Schönlein purpura[] Herein, we report a 6-month infant with a 7 days of fever and bilateral pleural effusion, elevated erythrocyte sedimentation rate, thrombocytosis, hypo-albominemia, normal[] Children: Gastroenteritis , mesenteric adenitis , Meckel's diverticulitis , intussusception , Henoch–Schönlein purpura , lobar pneumonia , urinary tract infection (abdominal[]

  • Myeloproliferative Disease

    Thrombotic thrombocytopenic purpura – This results in the reduction of platelet production and bleeding tendencies.[] One patient clearly represents a case of RARS with reactive thrombocytosis.[] As controls we considered 61 patients with reactive thrombocytosis referred to our Department in the same period of time.[]

  • Henoch-Schönlein Purpura

    Palpable purpura Palpable purpura , a manifestation of vascular inflammation, is the hallmark presentation of HSP presents regardless of age group.[] […] more common and severe in adults than in children; this involvement manifested as frequent hypertension and heavy proteinuria . [31] During acute attacks, leukocytosis, thrombocytosis[] Purpura, abdominal pain, and arthralgia comprise the classic triad. Renal involvement may be severe, especially in adults.[]

  • Acute Myelocytic Leukemia

    Purpura is characterized by flat bruises that are larger than petechiae but smaller than ecchymoses.[] Here we report a case of AML with thrombocytosis arising in a patient with this syndrome.[] Skin lesions of leukemia cutis tend to be non-specific and can range from papules, to nodules, to purpura.[]

  • Microscopic Polyangiitis

    Four years later, purpura, peripheral neuropathy, and increased levels of myeloperoxidase anti-neutrophil cytoplasmic antibodies (583 EU/mL) and C-reactive protein (2.27 mg[] […] conjunctivitis corneal ulceration skin lesions at high risk of DVT EXAMINATION pleural effusions pulmonary infiltrates skin vasculitis lesions INVESTIGATIONS leucocytosis thrombocytosis[] She also had microscopic polyangiitis clinically manifesting as crescentic glomerulonephritis and purpura with positive myeloperoxidase (MPO)-antineutrophil cytoplasmic antibodies[]

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