49 results
diagnosis management dermatology rheumatology differential oncology classification ucsdh dress drugreaction eosinophilia neurology rash signs skin algorithm cutaneous erythematosus gangrenosum infectiousdiseases
Pancytopenia - Differential Diagnosis Congenital Diseases: • GATA2 deficiency • Fanconi’s anemia • Wiskott-Aldrich syndrome • Ribosomopathy or telomeropathy Cancer: • Leukemia • Lymphoma Inflammatory
deficiency • Fanconi’s anemia ... Wiskott-Aldrich syndrome ... : • Systemic lupus ... consumption • Vitamin B12 ... deficiency Infections
Pyoderma Gangrenosum: Autoimmune disorder resulting in a vasculitis which causes slowly progressive ulceration of the skin.
vasculitis which causes ... a number of systemic ... Images #Clinical ... #Photo #Dermatology ... #SkinRash #Pyoderma
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Eosinophilia and Systemic ... Signs (DRESS Syndrome ... medication (in this case ... #Dermatology #SkinRash ... Eosinophilia #Legs #Photo
Drug Reaction with Eosinophilia and Systemic Signs (DRESS Syndrome): Formerly known as drug hypersensitivity reaction, DRESS represents
Eosinophilia and Systemic ... Signs (DRESS Syndrome ... medication (in this case ... #Dermatology #SkinRash ... Eosinophilia #Photo
BEE Syndromes - Non-inflammatory Causes Immune-mediated conditions affecting the Brain, Eye, and Ear Visual or auditory symptoms in
Non-inflammatory Causes ... central nervous system ... diagnosis and treatment ... • Lyme disease ... MRI lesions and clinical
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Clinical Presentation ... SLE], AOSD) • Infection ... with leukopenia, anemia ... Treatment: • Corticosteroids ... Diagnosis #Management #Hematology
Common Variable Immunodeficiency (CVID) What? CVID: Immunodeficiency disorder with hypogammaglobulinemia -> increased infection risk secondary to impaired B-cell
to 8 years Clinical ... autoimmune hemolytic anemia ... ) • Systemic granulomatous ... DDX - Other causes ... hypogammaglobulinemia #immunology #hematology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Clinical Presentation ... and petechiae Causes ... Idiopathic • Infections ... Treatment: ... #oncology #hematology
Erythema Annulare Centrifugum (EAC), This is erythema annulare centrifugum (EAC), one of the “figurate erythemas.” These lesions
, drugs, systemic ... disease, and malignancy ... Centrifugum #EAC #clinical ... #photo #dermatology ... #skinrash
Vancomycin induced Leukocytoclastic Vasculitis (LCV) of the Hand 70 M vertebral osteomyelitis on vancomycin and cefepime for
eosinophilia and systemic ... Churg-Strauss syndrome ... Vasculitis #LCV #Hand #skinrash ... #dermatology #clinical ... #photo
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