Diagnosis

To diagnose primary progressive aphasia, your doctor will review your symptoms and order tests.

Worsening communication difficulty without significant changes in thinking and behavior for a year or two is a hallmark of primary progressive aphasia.

Neurological examination

Doctors might conduct a neurological examination as well as a speech-language evaluation and a neuropsychological evaluation. Tests will measure your speech, language comprehension and skills, recognition and naming of objects, recall, and other factors.

Blood tests

Doctors might order blood tests to check for infections, measure medication levels or look for other medical conditions. Genetic tests can determine if you have genetic mutations associated with primary progressive aphasia or other neurological conditions.

Brain scans

MRI scans can help diagnose primary progressive aphasia, detect shrinking of certain areas of the brain and show which area of the brain might be affected. MRI scans can also detect strokes, tumors or other conditions that affect brain function.

Single-photon emission computerized tomography or PET scans can show blood flow or glucose metabolism abnormalities in areas of your brain.

Treatment

Primary progressive aphasia can't be cured, and there are no medications to treat it. However, some therapies might help improve or maintain your ability to communicate and manage your condition.

Speech and language therapy

Working with a speech-language pathologist, focusing primarily on efforts to compensate for eroding language skills, can be helpful. Although speech and language therapy hasn't been proved to slow progression of the condition, it can help you manage your condition.

Coping and support

Losing the ability to communicate is distressing and incredibly frustrating, both for the person with primary progressive aphasia and for friends and family. To help everyone involved cope:

  • Learn all you can about the condition
  • Have the person with the condition carry an identification card and other materials that can help explain the condition to others
  • Give the person time to talk
  • Speak slowly in simple, adult sentences and listen carefully
  • Take care of your personal needs — get enough rest and make time for social activities

Family members eventually may need to consider long-term care options for the person with primary progressive aphasia. Family members may also need to plan the person's finances and help make legal decisions to prepare for more-serious stages of the condition.

Support groups may be available for you and the person with primary progressive aphasia or related conditions. Ask your social worker or other members of your treatment team about community resources or support groups.

Preparing for your appointment

You might start by seeing your primary care provider. He or she may refer you to a doctor trained in brain and nervous system conditions (neurologist) or a speech-language pathologist.

What you can do

When you make the appointment, ask if there's anything you need to do in advance, such as fasting before having a specific test. Make a list of:

  • Your symptoms, including any that seem unrelated to the reason for your appointment
  • Key personal information, including major stresses, recent life changes and family medical history
  • All medications, vitamins and supplements you take, including doses
  • Questions to ask your doctor

Take a family member or friend along, if possible, to help with communication and to help you remember the information you receive.

For primary progressive aphasia, some questions to ask your doctor include:

  • What's likely causing my symptoms?
  • Other than the most likely cause, what are other possible causes?
  • What tests do I need?
  • Is my condition likely temporary or chronic?
  • What's the best course of action?
  • What are the alternatives to the primary approach you're suggesting?
  • I have other health conditions. How can I best manage them together?
  • Are there restrictions I need to follow?
  • Should I see a specialist?
  • Are there brochures or other printed material I can have? What websites do you recommend? 

Don't hesitate to ask other questions.

What to expect from your doctor

What happens during your appointment will vary depending on the type of doctor you see. Your doctor may ask:

  • When did your symptoms begin?
  • Have your symptoms been continuous or occasional?
  • How severe are your symptoms?
  • What, if anything, seems to improve your symptoms?
  • What, if anything, appears to worsen your symptoms?

Primary progressive aphasia care at Mayo Clinic

Aug. 08, 2017
References
  1. Primary progressive aphasia. National Aphasia Association. http://www.aphasia.org/aphasia-resources/primary-progressive-aphasia/. Accessed Oct. 18, 2015.
  2. Lee SE, et al. Frontotemporal dementia: Clinical features and diagnosis. http://www.uptodate.com/home. Accessed Oct. 18, 2015.
  3. Leger GC, et al. A review on primary progressive aphasia. Neuropsychiatric Disease and Treatment. 2007;3:745.
  4. Kirshner HS. Frontotemporal dementia and primary progressive aphasia, a review. Neuropsychiatric Disease and Treatment. 2014;10:1045.
  5. Mesulam M, et al. Primary progressive aphasia and the evolving neurology of the language network. Nature Reviews Neurology. 2014;10:554.
  6. Rogalski EJ, et al. Association between the prevalence of learning disabilities and primary progressive aphasia. JAMA Neurology. 2014;71:1576.
  7. Masulam M. Primary progressive aphasia. Dementia & Neuropsychologia. 2013;7:2.
  8. Family adjustment to aphasia. American Speech-Language-Hearing Association. http://www.asha.org/public/speech/disorders/FamilyAdjustmentAphasia/. Accessed Oct. 20, 2015.