Create issue ticket

1,898 Possible Causes for Cerebral Vasculitis or Vasculopathy, Subacute Clinical Course, Thrombocytosis

  • Sarcoidosis

    Although sarcoid is well recognized to affect the central nervous system, it is unusual in the form of cerebral vasculitis.[] The disease is extremely heterogeneous with an unpredictable clinical course.[] This case illustrates the intracranial vasculopathy as a rare complication of sarcoidosis.[]

  • Kawasaki Disease

    cerebral arteries.[] The typical laboratory features of Kawasaki disease, such as elevated erythrocyte sedimentation rate, leukocytosis, anemia, positive C-reactive protein and thrombocytosis[] […] presentation of KD varies over time, with the clinical course conventionally divided into 3 stages: acute, subacute, and convalescent (see the image below).[]

  • Granulomatosis with Polyangiitis

    […] conjunctivitis corneal ulceration skin lesions at high risk of DVT EXAMINATION pleural effusions pulmonary infiltrates skin vasculitis lesions INVESTIGATIONS leucocytosis thrombocytosis[] […] abnormalities in granulomatosis with polyangiitis may include: Raised white cell count (leucocytosis) Reduced haemoglobin (normocytic normochromic anaemia ) Raised platelet count (thrombocytosis[] In most patients with active disease, ESR and C-reactive protein are elevated, and serum albumin and total protein are decreased; anemia, thrombocytosis, and mild-to-moderate[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Henoch-Schönlein Purpura

    […] have been reported include esophageal stenosis, hemorrhagic pancreatitis, protein-losing enteropathy, pulmonary function abnormalities, pulmonary and pleural hemorrhage, thrombocytosis[] […] was more common and severe in adults than in children; this involvement manifested as frequent hypertension and heavy proteinuria. [31] During acute attacks, leukocytosis, thrombocytosis[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Acute Myelocytic Leukemia

    Here we report a case of AML with thrombocytosis arising in a patient with this syndrome.[] In particular, the histologic distinction between the “prefibrotic” stage of PMF (a stage often associated with marked thrombocytosis in the PB and granulocytic and atypical[] Trisomy 21: Down syndrome Defective DNA repair: Bloom syndrome, Fanconi anemia , and ataxia-telangiectasia Myeloproliferative syndromes: Polycythemia Vera , and essential thrombocytosis[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Essential Thrombocythemia

    […] primary Thrombocytosis familial thrombocytosis hereditary thrombocythemia hemorrhagic thrombocythemia Primary Thrombocythemia essential thrombocytemia ET essential thrombocytosis[] The patient was evaluated for thrombocytosis because he was in remission and suffering persistent thrombocytosis under treatment.[] Bone marrow biopsy in essential thrombocytosis showing increased megakaryocytes.[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Splenic Abscess

    Splenomegaly was present in 12 (67%), leukocytosis in 9 (50%), and thrombocytosis in 12 (67%) patients.[] Two months later he developed recurrent thrombophlebitis and fatal thromboembolism associated with thrombocytosis.[] Peripheral blood film confirmed neutrophilia and thrombocytosis. This finding was persistent on repeated samples.[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Ulcerative Proctitis

    Laboratory Parameters/Biomarkers Laboratory parameters that may be associated with active UC include anemia, reactive thrombocytosis, and hypoalbumenia.[] The onset of symptoms can be sudden or gradual. 8 The presence of anemia, thrombocytosis, or hypoalbuminemia may suggest inflammatory bowel disease, but most patients with[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Precursor-Cell Lymphoblastic Leukemia

    Myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis The criteria for MDS/MPN with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T; previously[] (RARS-T), has been accepted as a full entity, now termed MDS/MPN with ring sideroblasts and thrombocytosis in the 2016 revision.[] […] known as RARS-T) include thrombocytosis ( 450 10 9 /L) associated with refractory anemia, dyserythropoiesis in the BM with ring sideroblasts accounting for 15% or more of[]

    Missing: Cerebral Vasculitis or Vasculopathy
  • Psoas Abscess

    Diagnostic Tests & Interpretation Lab WBC 10,000/mL Anemia (hemoglobin Thrombocytosis (1,14) Elevations in blood urea nitrogen (BUN), sedimentation rate, and C-reactive protein[] Time Course of Clinical Symptoms Time Course of Presentation : typically subacute (over weeks) or chronic (over months) Latency to Diagnosis [ MEDLINE ] Median Latency to[] […] a low sensitivity and specificity Chest X-Ray : may demonstrate pleural effusion or elevated hemidiaphragm in some cases Tagged WBC Scan : may demonstrate psoas abscess Clinical[]

    Missing: Cerebral Vasculitis or Vasculopathy

Similar symptoms