Pick bodies

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Pick bodies are abnormal intracellular inclusions, primarily found within the neurons of certain areas of the brain. They are a hallmark of Pick's Disease, a type of Frontotemporal Dementia (FTD), which is characterized by progressive deterioration of behavior and language due to degeneration of the frontal and temporal lobes of the brain. The presence of Pick bodies is crucial for the neuropathological diagnosis of Pick's Disease.

Characteristics[edit | edit source]

Pick bodies are spherical, argyrophilic (silver-staining), and tau-positive inclusions that vary in size. They are composed of a dense, filamentous core surrounded by a clear halo. The primary component of these inclusions is an abnormal accumulation of the tau protein, which is hyperphosphorylated. This differs from the tau inclusions seen in Alzheimer's Disease, which are paired helical filaments, indicating a distinct pathological process.

Pathogenesis[edit | edit source]

The exact mechanism leading to the formation of Pick bodies is not fully understood. However, it is believed that mutations in the tau protein (MAPT) gene, which lead to an abnormal tau protein structure, play a significant role. This abnormal tau fails to bind properly to microtubules, leading to the accumulation of tau inclusions within the neurons. Over time, these inclusions disrupt normal cellular function and contribute to cell death.

Clinical Significance[edit | edit source]

The presence of Pick bodies is a key diagnostic feature of Pick's Disease. Symptoms of this condition can include changes in personality, behavior, and language. Early signs often involve emotional instability, loss of social inhibitions, or apathy, followed by progressive language dysfunction. As the disease advances, cognitive impairment becomes more pronounced.

Diagnosis[edit | edit source]

Diagnosis of Pick's Disease involves a combination of clinical assessment, imaging studies, and ultimately, confirmation through neuropathological examination. Magnetic Resonance Imaging (MRI) can show atrophy in the frontal and temporal lobes, but the definitive diagnosis requires the identification of Pick bodies in brain tissue, typically obtained post-mortem.

Treatment[edit | edit source]

There is currently no cure for Pick's Disease, and treatment is primarily supportive, focusing on managing symptoms and improving quality of life. Therapies may include medications to address behavioral issues, speech therapy to support communication skills, and various forms of supportive care.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD