What caused this man’s scalloped pupil?

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THE 46-year-old man’s symptoms were concerning but not particularly strange: He was losing weight, experiencing episodes of fainting and having trouble walking. But when doctors examined his eyes, they saw something odd: One of his pupils was smaller than the other, and it had an unusual, scalloped shape with irregular edges.
The strange shape of the man’s pupil turned out to be due to a rare genetic condition, according to a new report of the case.
Nearly two decades earlier, when the man was 29, he had a liver transplant to treat a genetic condi-tion called familial amyloid polyneuropathy (FAP), according to the report, published July 30 in the journal JAMA Neurology.
This condition causes abnormal deposits of a substance called amyloid to build up in the body’s tissues and organs, according to the U.S. National Library of Medicine(NLM). These deposits most frequently occur in the peripheral nervous system, or the nerves that connect the brain and spinal cord to muscles and cells that detect sensations through-out the body. As a result, the deposits often lead to a loss of sensation in the extremities, the NLM says, but the condition can also affect other systems and organs, including the heart, kidneys, eyes and gas-trointestinal tract.
In this man’s case, the deposits consisted of a protein called transthyretin, which is produced mainly by the liver, according to the new report, from doctors at the Centre Hospitalier de Luxem-bourg.
Because of this, a liver transplant is recom-mended as the “gold standard” of care for patients with this form of FAP, according to the National Institutes of Health’s Genetic and Rare Diseases Information Center. A liver transplant can slow or halt the progression of neurological symptoms. But this protein is also produced in other parts of the body, including the eye, which means that even with a liver transplant, patients may still experience symptoms, including eye problems.
In patients with this type of FAP, the odd shape of the pupil results from two factors: amyloid de-posits in the lens of the eye and abnormalities in the autonomic nervous system (the system that controls involuntary body functions), said Dr. Mark Fromer, an ophthalmologist at Lenox Hill Hospital in New York City, who was not involved with the man’s case. Both of these problems result from the under-lying genetic condition.Fromer added that this condition is “extremely rare” and that the last time he saw a case like this was around 35 years ago,

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