Leukemias Overview: ALL, CML, AML, APML, CLL
Acute leukemias > 20% blasts in the peripheral blood smear or on bone marrow leading to a more rapid onset of symptoms.
Chronic leukemia < 20% blasts with a relatively chronic onset of symptoms.
ALL (Acute Lymphoblastic Leukemia):
• Lymphocytes - T or B lineage
• Immature
• Age: 10
• 75% usually under 6 years age
• 75% of ALL is of B-cell lineage
ALL Symptoms:
• Malaise, bleeding, infections, bone pain
• Bulky lymphadenopathy
• Blast cells - Blood and Bone marrow
• Mature B-cell ALL can present as extramedullary disease, including gastrointestinal or testicular involvement
• T-cell ALL: mediastinal mass
• Rapidly rising blast cells - Blood & BM
• Bulky lymphadenopathy
• Cytopenia -> BM involvement
• 30%: CNS involvement
CML (Chronic Myeloid Leukemia):
• Neutrophils (myeloid)↑
• Mature
• Age: 40-60
• + (9;22) Philadelphia - BCR-ABL
• ↑ Tyrosine Kinase activity
• ↓ LAP Score
• CML -> AML: Blast crises
• Blasts > 10% leukocytes
Blast Phase:
• Headaches, bone pain, fever, joint pain, bleeding, infections, and lymphadenopathy
CML Findings:
• Splenomegaly
• ↑ Leukocyte count ↑ PLT
• ↑ PBS: Granulocytic cells in all phases of maturation
• (Peripheral eosinophilia, basophilia, and thrombocytosis)
CML Symptoms:
• Fatigue, weight loss, abdominal fullness (splenomegaly), night sweats, bleeding
• Pruritis after hot bath/showers
• Lymphadenopathy
AML (Acute Myeloid Leukemia):
• Neutrophils
• Immature/Myeloblasts
• Age: 50-60
• Auer Rods
Significant ↓ PLT: Petechiae, bruising, bleeding, infection
RARE - Lymphadenopathy/HSM
Leukocyte Count:
• ↑ Can develop leukostasis syndrome: CNS manifestations, hypoxia, CXR - infiltrates (anemia, thrombocytopenia, or functional neutropenia)
• Bone pain, dyspnea, gingival hypertrophy
• Leukemia cutis (violaceous, nontender cutaneous plaques)
AML Dx:
• ↑ Leukocyte count
• ↓Hg & PLT
• Peripheral smear: Blasts
APML (Acute Promyelocytic Leukemia):
• Poorly differentiated leukocytes + distinctive primary granules
• t(15;17) translocation
• Significant bleeding: Fibrinolysis & DIC
• Tumor lysis syndrome: Develops in treated pts. Intracellular Urate, Potassium and Phosphorus
CLL (Chronic Lymphocytic Leukemia):
• Lymphocytes
• Mature
• Age: 60-80
Clonal Accumulation of Mature B Lymphocytes:
• In the peripheral blood, bone marrow and secondary lymphoid organs
When Cancer Cells are in the Lymph Nodes:
• Small lymphocytic lymphoma (SLL)
CLL Symptoms:
• Lymphadenopathy
• HSM
• Fevers
• Drenching night sweats/fatigue
• Exaggerated response to mosquito bites
CLL -> Invade Skin: Leukemia cutis
Labs:
• Lymphocytosis/Cytopenias
• AIHA, ITP, Agranulocytosis
• Hypogammaglobulinemia, smudge cells
Richter's Transformation:
• Complication of Chronic Lymphocytic Leukemia (CLL) and/or Small Lymphocytic Lymphoma (SLL)
• Sudden transformation of the CLL/SLL into a significantly more aggressive form of large cell lymphoma
#Leukemia #Hematology #Oncology #Diagnosis
Lyme Disease - Diagnosis and Management Summary
Lyme Disease Epidemiology:
- Spirochete
- Reservoir: small mammals & birds
- Transmitted by Ixodes tick
- Ixodes Scapularis in eastern and north regions of North America
- Bimodal distribution:
- 5-14 years old
- 45-55 years old
- Peak incidence: Summer months
Lyme Disease Clinical Progression
1. Early Localized Disease:
- Erythema Chronicum Migrans
- Flu-like illness/fatigue
- Swollen lymph nodes
- Headache/stiff neck
- Sore throat
2. Early Disseminated - Weeks to Months:
- Neurological
- Carditis
3. Late Disease (Months to Years):
- Arthritis
- Neurological features
Lyme Disease Complications:
• Neuroborreliosis:
- Meningococcal-radiculitis
- Meningitis
- Meningo-encephalitis
- Bell’s palsy
- Vision changes
- Pain, weakness, numbness
• Carditis:
- AV block: Fluctuating first-second-third degree block
- Myopericarditis
- LV failure
- Pericarditis
• Ocular:
- Conjunctivitis
- Keratitis
- Iridocyclitis
- Retinal vasculitis
- Uveitis
• Neuro:
- Lyme encephalopathy
- Polyneuropathy
• Arthritis:
- Large joints
- Joint swelling/pain
Lyme Disease Diagnosis:
1. Rash: distinctive enough to make diagnosis if living in an endemic area
2. ELISA: detects antibodies to B. Burgdorferi
3. WESTERN BLOT: to confirm the dx. Detects antibodies to proteins of B. Burgdorferi
4. LP-CSF: lymphocytic pleocytosis
Lyme Disease Treatment:
1. Early: Doxycycline, amoxicillin 10-14 days
2. Early Disseminated: Doxycycline, amoxicillin or ceftriaxone for 14-28 days
3. Late:
- IV ceftriaxone, cefotaxime or PCN G for 21 days for Neuro involvement
- Oral doxycycline without Neuro disease
By Dr. Ravi Singh @rav7ks
#Lyme #Disease #Diagnosis #Management #treatment
Causes of Headache - Differential Diagnosis Algorithm
Primary: Tension, Migraine, Cluster
Extracranial: Medications, Sinusitis, TMJ disorder, Cervicogenic, Glaucoma, Giant cell arteritis
Vascular: Hypertension, Stroke, Venous trrombosis, Dissection, Aneurysm, Hemorrhage, Vasculitis, PRES, Moyamoya
Infectious: Meningitis, Encephalitis, Abscess, Septic emboli, Toxoplasmosis
Tumor: Primary, Metastatic disease
CSF: Hydrocephalus, Pseudotumor Cerebri, Low CSF
Other: Trigeminal neuralgia, Post-traumatic
by Lauren Banaszak, MD @LaurenBzak via @uw_IMresidency
#Headache #Differential #Diagnosis #Causes #algorithm
Cephalosporin Antibiotics
• First Generation: Cefazolin, Cefadroxil, Cephalexin
• Second Generation: Cefuroxime sodium, Cefuroxime axetil
• Third Generation: Cefdinir, Cefixime, Cefotaxime, Ceftazidime, Ceftibuten, Ceftriaxone
• Fourth Generation: Cefepime
#Cephalosporin #Antibiotics #comparison #pharmacology #classification