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diagnosis management rheumatology alkaline alp colitis cryofibrinogenemia cutaneous cvid dermatology erythematosus eschar gca giantcell hemeonc hemophagocytic hepatology hlh hyophosphatasia hypogammaglobulinemia
Mild-to-Moderate Ulcerative Colitis - Management Algorithm Curcumin: • Natural phytochemical from turmeric • 2g/day divided in 2-3
Nissle • VSL#3: ↑ clinical ... delivery to the colon ... • Budesonide Foam ... PR, Enema PR • ... suppository or foam
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
infection risk secondary ... to 8 years Clinical ... autoimmune hemolytic anemia ... DDX - Other causes ... hypogammaglobulinemia #immunology #hematology
Giant cell arteritis (GCA) Giant cell arteritis (GCA) definition: Most common systemic inflammatory vasculitis in older adults
definition: Most common ... particularly those coming ... Diagnosis = clinical ... systemic complaints- anemia ... treatment once you commit
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Secondary form associated ... Diagnosis: • + Clinical ... cryoglobulins • Negative causes ... to medium-sized arteries ... #hematology
Low Alkaline Phosphatase - Hypophosphatasia Is Low Alkaline Phosphatase Of Clinical Importance? ALP enzyme- Discovered in 1923 Low
Phosphatase Of Clinical ... Adult form: Less ... pain • loss of secondary ... • Pernicious anemia ... Phosphatase: • Other causes
SLE (Systemic Lupus Erythematosus) Suspect: Clinical evidence of (fatigue, rash, photosensitivity, inflammatory arthritis, weight loss, and fever) and
) Suspect: Clinical ... Malignancy (e.g. hematologic ... vein thrombosis Hematologic ... lymphopenia, low PLT • Anemia ... Kidney disease common
Sjogren's Syndrome Overview Epidemiology: • F > M: 9:1 • 5-6th Decades (can be any age) Autoimmune exocrinopathy multisystemic disease
other diseases • Secondary ... Hypocomplementemia • Can cause ... salivary ducts Clinical ... Nephrogenic DI Hematologic ... Arthralgia and Arthritis
Polymyalgia Rheumatica (PMR) Diagnosis and Management Summary WHAT? • Polymyalgia rheumatica (PMR) is a common systemic inflammatory
disease of unknown cause ... CLINICAL: • Physical ... for giant cell arteritis ... diagnosed based on clinical ... • Normocytic anemia
Cutaneous Mucormycosis Eschar 30 M HIV cd4 10 VL 30k traumatic injury of arm few months ago
matter, soil, wood, cotton ... trauma, aplastic anemia ... had success combing ... Mucormycosis #Eschar #dermatology ... #skin #clinical
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... STX11, STXBP2 • Secondary ... • Common Signs ... - Cytopenias (anemia ... Diagnosis #Management #Hematology
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