Gout is a heterogeneous group of diseases characterized by
hyperuricemia (plasma urate level above 6.8 mg/dL) and urate crystal deposition in joints and kidneys.
Depending on the etiology of hyperuricemia.
● Primary (idiopathic): Hyperuricemia occurs without any
other disease. ● Secondary: Hyperuricemia occurs in association with another illness.
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3 MEDICAL GLOBE E-LEARNING MEDICINE SESSION ● Age: Gout usually presents after 30 years of age. ● Duration of the hyperuricemia: Usually not less than ● 20–30 years. ● Genetic predisposition: Primary gout is of multi- factorial inheritance and runs in families. ● Heavy alcohol intake. ● Obesity. ● Drugs (e.g thiazides) which reduce excretion of urate. ● Lead toxicity.
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5 MEDICAL GLOBE E-LEARNING MEDICINE SESSION 6 MEDICAL GLOBE E-LEARNING MEDICINE SESSION 7 MEDICAL GLOBE E-LEARNING MEDICINE SESSION 8 MEDICAL GLOBE E-LEARNING MEDICINE SESSION MORPHOLOGY Acute inflammation: It is characterized by edema, congestion and dense infiltration of synovium by neutrophils. Few lymphocytes, plasma cells, and macrophages may also be seen.
Monosodium urate (MSU) crystals
● They are long, slender, and needle shaped. ● They are found in the cytoplasm of the neutrophils and are arranged in small clusters in the synovium.
If not resolved it leads to Tophi.
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Tophi: Pathognomonic feature of gout.
Lesions consisting of large aggregates of urate crystals,
surrounded by inflammatory reactions are known as tophi and are the pathognomonic of gout.
Microscopy: They consist of aggregations of urate crystals
surrounded by macrophages, lymphocytes, and foreign- body giant cells.
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