Diagnosing Skin Cancers with Light, Not Scalpels

Old Way: Patient asks “Doc is this mole on my face cancerous?”
Doc says “Let me cut a chunk out and send it to the lab. We’ll know if its cancerous in a few days.”
New Way: Patient asks “Doc is this mole on my face cancerous?
Doc says “Let me touch it with my fiber optic cable and develop a 3D cellular-scale image. I’ll have you diagnosed in just a few femtoseconds…
From Duke University:

“The standard way physicians do a diagnosis now is to cut out a mole and look at a slice of it with a microscope,” said Warren Warren, the James B. Duke Professor of chemistry, radiology and biomedical engineering, and director of Duke’s new Center for Molecular and Biomedical Imaging. “What we’re trying to do is find cancer signals they can get to without having to cut out the mole.
“This is the first approach that can target molecules like hemoglobin and melanin and get microscopic resolution images the equivalent of what a doctor would see if he or she were able to slice down to that particular point,” Warren said.
The distributions of hemoglobin, a component of red blood cells, and melanin, a skin pigment, serve as early warning signs for skin cancer growth. But because skin scatters light strongly, simple microscopes cannot be used to locate those molecules except right at the surface. Although laser methods have been developed to probe deeper down for some other molecules that can be made to glow, both melanin and hemoglobin remain dark and inaccessible using those methods.
Warren’s group has now developed a technology for coaxing both hemoglobin and melanin inside questionable skin moles to emit light by exciting them with highly controlled laser pulses.
The innovation uses a delicate interplay between two laser beams, each emitting a different color of light. To keep the skin from overheating in the process, the lasers must also be able to pulse on for only femtoseconds — a thousand trillionths of a second — at a time.
The glow of the hemoglobin- and melanin-bearing structures can be magnified by a microscope outside the skin and manipulated by computers to create cellular-scale images. The noninvasive technique could enable doctors to see as much as a millimeter below the skin’s surface — more than enough for diagnosis, Warren said.
“What this is leading to is for a doctor to be able to touch a mole with a fiberoptic cable and characterize what is going on inside it,” he said.
“Today, if you visit a dermatologist, he or she will probably see many moles on your body. But the difficulty is trying to figure out which of those, if any, are dangerous.”
Warren’s group demonstrated at a March conference of the American Physical Society how the technique can visualize melanin from inside an excised human melanoma.

Press release: Diagnosing Skin Cancers with Light, Not Scalpels …