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Symptoms and Signs – Differential Diagnosis of Arachnodactyl
Ehler.s-Danlos syndrome
Homocysteinuria
Marfan's syndrome
Normal finding
Ehler.s-Danlos syndrome
Homocysteinuria
Marfan's syndrome
Normal finding
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Symptoms and Signs – Differential Diagnosis of Arm pain
Trauma, strain injury
Arthritis (See Monoarthralgia)
Neurological: cervical spinal cord compression (prolapsed disc, cervical spondylosis, tumours)
Brachia! plexus involvement: apical lung cancer, cervical rib
Peripheral neuropathies
Carpal tunnel syndrome
Vascular: subclavian artery stenosis, arterial/venous thrombosis, embolism
Bone: tumours (primary, secondary: lung, breast, prostate, kidney, thyroid)
Referred cardiac pain
See also Shoulder pain
Trauma, strain injury
Arthritis (See Monoarthralgia)
Neurological: cervical spinal cord compression (prolapsed disc, cervical spondylosis, tumours)
Brachia! plexus involvement: apical lung cancer, cervical rib
Peripheral neuropathies
Carpal tunnel syndrome
Vascular: subclavian artery stenosis, arterial/venous thrombosis, embolism
Bone: tumours (primary, secondary: lung, breast, prostate, kidney, thyroid)
Referred cardiac pain
See also Shoulder pain
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Symptoms and Signs – Differential Diagnosis of Apex beat
Heaving (pressure loaded)
Aortic stenosis (See Aortic stenosis)
Systemic hypertension
Thrusting (volume loaded)
Mitral regurgitation
Aortic regurgitation
Tapping
Apex beat not palpated
COPD
Dextrocardia
L-sided pleural effusion
L-sided pneumothorax
Large pericardial Effusion
Mitral stenosis
Obesity, muscular chest wall
Heaving (pressure loaded)
Aortic stenosis (See Aortic stenosis)
Systemic hypertension
Thrusting (volume loaded)
Mitral regurgitation
Aortic regurgitation
Tapping
Apex beat not palpated
COPD
Dextrocardia
L-sided pleural effusion
L-sided pneumothorax
Large pericardial Effusion
Mitral stenosis
Obesity, muscular chest wall
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Symptoms and Signs – Differential Diagnosis of ANA
Normal population (S-8%)
Other diseases: chronic active hepatitis, diabetes, Waldenstrom's macroglobulinaemia, myasthenia gravis
Polyarteritis nodosa (20%)
Polymyositis (40%)
Rheumatoid arthritis (60%)
Sjogren's syndrome (80%)
SLE (9S%), drug-induced lupus (100%)
Systemic sclerosis (90%)
Normal population (S-8%)
Other diseases: chronic active hepatitis, diabetes, Waldenstrom's macroglobulinaemia, myasthenia gravis
Polyarteritis nodosa (20%)
Polymyositis (40%)
Rheumatoid arthritis (60%)
Sjogren's syndrome (80%)
SLE (9S%), drug-induced lupus (100%)
Systemic sclerosis (90%)
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Symptoms and Signs – Differential Diagnosis of Aplastic Anemia
Inherited: Fanconi anaemia, dyskeratosis congenita
Idiopathic
Acquired: drugs (cytotoxics, chloramphenicol, gold, methotrexate), chemicals (parathion, benzene), radiation, viral infection (B19 parvovirus, HIV, hepatitis, measles), paroxysmal nocturnal haemoglobinuria, sepsis
Inherited: Fanconi anaemia, dyskeratosis congenita
Idiopathic
Acquired: drugs (cytotoxics, chloramphenicol, gold, methotrexate), chemicals (parathion, benzene), radiation, viral infection (B19 parvovirus, HIV, hepatitis, measles), paroxysmal nocturnal haemoglobinuria, sepsis
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Symptoms and Signs – Differential Diagnosis of Raised in Amylase
Acute abdomen: peptic ulcer, perforation, intestinal obstruction, ruptured
Diabetic ketoacidosis
ectopic pregnancy
Macroamylasaemia: amylase is complexed with another protein, e.g. immunoglobulin and its renal clearance is reduce
Morphine (spasm of sphincter of Oddi)
Pancreatitis (acute)
Renal failure
Salivary gland disorders: calculi, mumps
Acute abdomen: peptic ulcer, perforation, intestinal obstruction, ruptured
Diabetic ketoacidosis
ectopic pregnancy
Macroamylasaemia: amylase is complexed with another protein, e.g. immunoglobulin and its renal clearance is reduce
Morphine (spasm of sphincter of Oddi)
Pancreatitis (acute)
Renal failure
Salivary gland disorders: calculi, mumps
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Symptoms and Signs – Differential Diagnosis of Normocytic
Anaemia of chronic disease (chronic infection, inflammatory/connective tissue diseases, malignancy)
Bone marrow failure
Haemolytic anaemia (may also cause macrocytic anaemia)
Hypothyroidism (may also cause macrocytic anaemia)
Pregnancy
Renal failure
Anaemia of chronic disease (chronic infection, inflammatory/connective tissue diseases, malignancy)
Bone marrow failure
Haemolytic anaemia (may also cause macrocytic anaemia)
Hypothyroidism (may also cause macrocytic anaemia)
Pregnancy
Renal failure
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Symptoms and Signs – Differential Diagnosis of Microcytic Anaemia
Anaemia of chronic disease (often normocytic, but may be microcytic)
Iron deficiency: blood loss (GI [e.g. peptic ulcer, malignancy), urogenital [e.g. menorrhagia, haematuria)), hookworm (Ancylostroma duodenale)
Lead poisoning
Reduced absorption (gastrectomy, small bowel disease),increased demands (growth, pregnancy), reduced intake (e.g. vegans)
Sideroblastic anaemia: congenital (X-linked), alcohol, drugs (isoniazid, chloramphenicol), lead, myelodysplasia
Thalassaemia
Anaemia of chronic disease (often normocytic, but may be microcytic)
Iron deficiency: blood loss (GI [e.g. peptic ulcer, malignancy), urogenital [e.g. menorrhagia, haematuria)), hookworm (Ancylostroma duodenale)
Lead poisoning
Reduced absorption (gastrectomy, small bowel disease),increased demands (growth, pregnancy), reduced intake (e.g. vegans)
Sideroblastic anaemia: congenital (X-linked), alcohol, drugs (isoniazid, chloramphenicol), lead, myelodysplasia
Thalassaemia
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Symptoms and Signs – Differential Diagnosis of Macrocytic Anemia
Alcohol
Folate/B 12 deficiency
Haemolytic anaemia
Hypothyroidism
Liver disease
Myelodysplasia
Alcohol
Folate/B 12 deficiency
Haemolytic anaemia
Hypothyroidism
Liver disease
Myelodysplasia
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Symptoms and Signs – Differential Diagnosis of Haemolytic Anemia
Hereditary
Metabolic defects: pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency
Haemoglobinopathies: sickle cell anaemia, thalassaemia Membrane defects: spherocytosis, elliptocytosis
Acquired
Paroxysmal nocturnal haemoglobinuria, secondary to liver and renal disease
Non-immune: trauma: microangiopathic haemolytic anaemia (TIP, HUS, DIC, malignant hypertension, pre-eclampsia), artificial heart valves, March haemoglobinuria
Infection: malaria, clostridia
Drugs: penicillin, quinidine
Autoimmune: Warm antibodies (idiopathic, SLE, lymphoma, drugs, e.g. methyldopa), Cold antibodies (idiopathic, infections, e.g. Mycoplasma sp., EBV, other viruses, lymphoma)
Alloimmune: Transfusion reaction, haemolytic disease of newborn
Hereditary
Metabolic defects: pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency
Haemoglobinopathies: sickle cell anaemia, thalassaemia Membrane defects: spherocytosis, elliptocytosis
Acquired
Paroxysmal nocturnal haemoglobinuria, secondary to liver and renal disease
Non-immune: trauma: microangiopathic haemolytic anaemia (TIP, HUS, DIC, malignant hypertension, pre-eclampsia), artificial heart valves, March haemoglobinuria
Infection: malaria, clostridia
Drugs: penicillin, quinidine
Autoimmune: Warm antibodies (idiopathic, SLE, lymphoma, drugs, e.g. methyldopa), Cold antibodies (idiopathic, infections, e.g. Mycoplasma sp., EBV, other viruses, lymphoma)
Alloimmune: Transfusion reaction, haemolytic disease of newborn