Apparatus and method for skin lesion examination

Claim 3

A portable nevoscope for examining in situ a skin lesion of a patient, comprising: (a) a transparent, cup-like specimen housing having a central axis and a base with a central aperture for receiving a specimen of skin of a patient, said specimen of skin containing said lesion to be examined; (b) a transillumination means for transilluminating said specimen surrounding said specimen housing and for transmitting light in a converging ring of light into the skin of the patient around lesion to form a point of light at a point below said lesion thereby to uniformly transilluminate said lesion from within the skin of the patient; (c) a means for establishing a vacuum in said cup-like specimen housing to facilitate coupling between said transillumination means and the skin of the patient surrounding said lesion; (d) a mirror housing positioned around said specimen housing, said mirror housing containing a plurality of mirrors positioned for viewing mirror images of said lesion in said specimen housing each mirror having a tilt angle, said mirror housing being rotatable about said central axis to provide multiple positions for viewing images of said lesion, each mirror having a means for adjusting the tilt angle of said mirror with respect to said central axis to allow each mirror to be tilted thereby to obtain at any position of said mirror housing images at different angles of a portion of said lesion; and (e) a lens housing coupled with said mirror housing, said lens housing having a lens and an eyepiece for viewing said mirror images of said specimen of skin within said specimen housing, said rotatable mirror housing and said rotatable mirrors enabling said nevoscope to obtain multiple images of said lesion.

Claim 4

A portable nevoscope for examining in situ a skin lesion of a patient, comprising: (a) a transparent, cup-like specimen housing having a central axis and a base with a central aperture for receiving a specimen of skin of a patient, said specimen of skin containing said lesion to be examined; (b) a transillumination means for transilluminating said specimen surrounding said specimen housing and for transmitting light in a converging ring of light into the skin of the patient around lesion to form a point of light at a point below said lesion thereby to uniformly transilluminate said lesion from within the skin of the patient; (c) a means for establishing a vacuum in said cup-like specimen housing to facilitate coupling between said transillumination means and the skin of the patient surrounding said lesion; (d) a mirror housing positioned around said specimen housing, said mirror housing containing a plurality of mirrors positioned for viewing mirror images of said lesion in said specimen housing each mirror having a tilt angle, said mirror housing being rotatable about said central axis to provide multiple positions for viewing images of said lesion, each mirror having a means for adjusting the tilt angle of said mirror with respect to said central axis to allow each mirror to be tilted thereby to obtain at any position of said mirror housing images at different angles of a portion of said lesion; and (e) a lens housing coupled with said mirror housing, said lens housing having a lens and an eyepiece for viewing said mirror images of said specimen of skin within said specimen housing, said rotatable mirror housing and said rotatable mirrors enabling said nevoscope to obtain multiple images of said lesion.

Claim 5

The nevoscope of claim 2 wherein the lens provides a depth of focus sufficient to focus all images seen through the nevoscope.

Claim 6

The nevoscope of claim 2 wherein said mirror tilt adjusting means comprises: (a) a plurality of spring chambers mounted on an inner wall of said mirror housing, each of said spring chambers mounted at a position radially outward from a lower central portion of one of said mirrors; (b) a plurality of telescopic arms, each of said telescopic arms horizontally mounted in one of said spring chambers and attached to one of said mirrors; (c) a plurality of pivot arms, each of said pivot arms mounted between the inner wall of said mirror housing and a central portion of one of said mirrors; and (d) a plurality of adjustable arms, each of said stop arms extending through the inner wall of said mirror housing radially inward to a top edge of one of said mirrors, each said adjustable stop arm cooperating with an associated said telescopic arm to permit the tilt angle of the associated mirror to be adjusted.

Claim 7

The nevoscope of claim 2 further comprising: (a) an entrance pupil mounted in the lens housing between the lens and the cup-like specimen housing.

Claim 8

The nevoscope of claim 2 further comprising a light source mounted in a wall of said lens housing at an angle to provide surface illumination of the specimen of skin in said cup-like specimen housing.

Claim 9

The nevoscope of claim 2 wherein the means for establishing a vacuum is a suction device inserted into said specimen housing.

Claim 10

The nevoscope of claim 7 wherein said suction device is an inlet tube having a first end inserted into said cup-like specimen housing and a second end attached to a squeeze bulb.

Claim 11

The nevoscope of claim 2 wherein said transillumination means comprises: (a) an illuminator ring positioned around said cup-like specimen housing; and (b) a plurality of fiber optic filaments uniformly dispersed in said illuminator ring and positioned to direct light onto the skin of the patient surrounding said lesion.

Claim 12

The nevoscope of claim 9 wherein said fiber optic filaments are directed downward at a 45° angle.

Claim 13

The nevoscope of claim 2 further comprising a camera mounted to said eyepiece wherein said camera can receive images through said eyepiece.

Claim 14

The nevoscope of claim 11 further comprising a digitizer electronically coupled to said camera.

Claim 15

The nevoscope of claim 12 further comprising an image processor coupled to said digitizer.

Claim 16

A portable nevoscope comprising: (a) a lens housing having an upper end and lower end, said lens housing containing an eyepiece cylinder mounted in the upper end; (b a lens mounted in an axial position in said lens housing; (c) a mirror housing having an upper end and a lower end, the upper end of said mirror housing being mechanically coupled with the lower end of said lens housing, said mirror housing further having a central axis; (d) a plurality of mirrors spaced apart and mounted within said mirror housing near a wall of said mirror housing, each of said plurality of mirrors oriented to reflect toward said central axis of said mirror housing, each of aid mirrors including a means for tilting the mirror with respect to said central axis; (e) a transparent cup-like specimen housing with a central aperture foe receiving a specimen of skin containing a skin lesion to be examined, said specimen housing centrally positioned in the lower end of said mirror housing, said mirror housing being rotatable with respect to said specimen housing to permit said mirrors to be rotated to multiple positions around said lesion for obtaining multiple images of said lesion, said specimen housing having a top and a base; (f) an extension tube having an inner end and an outer end, the inner end of said extension tube extending into said specimen housing and the outer end of said extension tube extending out of said mirror housing; (g) a means attached to the outer end of said extension tube for pulling a vacuum in said specimen housing; (h) an illuminator ring positioned around the lower end of said mirror housing, said vacuum pulling means obtaining uniform contact between said illuminator ring and the skin of the patient surrounding said lesion to facilitate coupling of light into the skin of the patient; and (i) a plurality of fiber optic filaments uniformly dispersed in said illuminator ring and positioned to direct light into the skin of the patient surrounding said lesion, said illuminator ring transmitting a converging ring of light into the skin of a patient to form a point of light at a point below said lesion thereby to uniformly transilluminate said lesion from within the skin of the patient.

Claim 17

A portable nevoscope comprising: (a) a lens housing having an upper end and lower end, said lens housing containing an eyepiece cylinder mounted in the upper end; (b a lens mounted in an axial position in said lens housing; (c) a mirror housing having an upper end and a lower end, the upper end of said mirror housing being mechanically coupled with the lower end of said lens housing, said mirror housing further having a central axis; (d) a plurality of mirrors spaced apart and mounted within said mirror housing near a wall of said mirror housing, each of said plurality of mirrors oriented to reflect toward said central axis of said mirror housing, each of aid mirrors including a means for tilting the mirror with respect to said central axis; (e) a transparent cup-like specimen housing with a central aperture foe receiving a specimen of skin containing a skin lesion to be examined, said specimen housing centrally positioned in the lower end of said mirror housing, said mirror housing being rotatable with respect to said specimen housing to permit said mirrors to be rotated to multiple positions around said lesion for obtaining multiple images of said lesion, said specimen housing having a top and a base; (f) an extension tube having an inner end and an outer end, the inner end of said extension tube extending into said specimen housing and the outer end of said extension tube extending out of said mirror housing; (g) a means attached to the outer end of said extension tube for pulling a vacuum in said specimen housing; (h) an illuminator ring positioned around the lower end of said mirror housing, said vacuum pulling means obtaining uniform contact between said illuminator ring and the skin of the patient surrounding said lesion to facilitate coupling of light into the skin of the patient; and (i) a plurality of fiber optic filaments uniformly dispersed in said illuminator ring and positioned to direct light into the skin of the patient surrounding said lesion, said illuminator ring transmitting a converging ring of light into the skin of a patient to form a point of light at a point below said lesion thereby to uniformly transilluminate said lesion from within the skin of the patient.

Claim 18

The nevoscope of claim 14 wherein the axial position of said lens within said lens housing is adjustable.

Claim 19

The nevoscope of claim 14 further comprising a light source adjustably mounted in the lower end of said lens housing such that orientation of said light source can be varied.

Claim 20

The nevoscope of claim 14 further comprising: (a) an entrance pupil mounted in said lens housing below said lens; and (b) a focus correcting plate mounted in the upper end of said mirror housing.

Claim 21

The nevoscope of claim 17 further comprising: (a) a camera mounted above said eyepiece cylinder wherein said camera can receive images through said eyepiece; (b) a digitizer electronically coupled to said camera; and (c) an image processor electronically coupled to said digitizer.

Claim 22

An in situ method of examining a nevi in the skin which comprises the steps of: (a) isolating a specimen of skin which includes the nevi; (b) uniformly transilluminating the nevi and the skin surrounding said nevi with a converging ring of light so as to form a point of light at a point below said nevi thereby to uniformly transilluminate said nevi from within the skin; (c) recording images of the transilluminated nevi from a direct image and from reflected mirror images obtained at a plurality of angles at positions around said nevi; and (d) generating a three-dimensional reconstruction of said nevi by computerized tomography from the recorded images thereby to obtain depth information of the nevi.

Claim 23

An in situ method of examining a nevi in the skin which comprises the steps of: (a) isolating a specimen of skin which includes the nevi; (b) uniformly transilluminating the nevi and the skin surrounding said nevi with a converging ring of light so as to form a point of light at a point below said nevi thereby to uniformly transilluminate said nevi from within the skin; (c) recording images of the transilluminated nevi from a direct image and from reflected mirror images obtained at a plurality of angles at positions around said nevi; and (d) generating a three-dimensional reconstruction of said nevi by computerized tomography from the recorded images thereby to obtain depth information of the nevi.

Claim 24

The method of claim 19, including the step of applying suction to the specimen of skin to provide uniform coupling of said ring of light into the skin surrounding said nevi.

Claim 27

The method of claim 21 wherein said color filter is green.

Claim 28

The method of claim 21 wherein said color filter is red.

Claim 29

The method of claim 21 wherein said color filter is blue.

Claim 30

The method of claim 21 further comprising the steps of: (a) computing a thickness of said skin lesion; and (b) computing a size of said skin lesion.

Claim 31

The method of claim 21 further comprising the steps of analyzing the color and texture characteristics of said color component images wherein said step of analyzing comprises the steps of: (a) measuring a brightness level of each pixel in each of said color component images; and (b) computing a spectrum histogram from said brightness levels.

Claim 32

The method of claim 21 further comprising the step of detecting a boundary of said skin lesion.

Claim 33

The method of claim 27 wherein the step of detecting the boundary of said skin lesion comprises the steps of: (a) selecting a subimage lying entirely within said skin lesion from said digitized image; (b) selecting a subimage lying entirely with a background from said digitized image; (c) computing a histogram of said skin lesion subimage; (d) computing a histogram of said background subimage; (e) selecting a skin lesion gray scale range from said histogram of said skin lesion subimage; (f) listing pixel coordinates of boundary pixels located near a boundary of the skin lesion subimage and the background subimage; (g) selecting a minimum acceptable expansion pass rage, known as X; (h) recording the gray scale values for a pixel array comprising each pixel that is contiguous to said boundary pixels; (i) computing a percentage of pixel gray scale values recorded in step (h) that fall within said skin lesion gray scale range, said percentage to be known as Y; (j) assigning each of said boundary pixels where Y is greater than X to said skin lesion; (k) recomputing said skin lesion gray scale range; (l) assigning each of said boundary pixels where Y is less than X to said background; (m) redefining said boundary pixels to include only pixels where Y is greater than X; (n) recording the gray scale values for a pixel array comprising each pixel that is contiguous to said boundary pixels; (o) computing a percentage of pixel gray scale values recorded in step (n) that fall within said recomputed skin lesion gray scale range, said percentage to be known as Y; (p) assigning each of said boundary pixels where Y is greater than X to said skin lesion; (q) recomputing said skin lesion gray scale range; (r) assigning each of said boundary pixels where Y is less than X to said background; and (s) repeating steps (m) through (r) until no more boundary pixels exist where Y is greater than X.

Claim 34

The method of claim 27 wherein the step of detecting the boundary of said skin lesion comprises the steps of: (a) visually approximating a location of the skin lesion boundary; (b) computing a gray scale range of a subimage lying entirely within said skin lesion; (c) computing a gray scale range of a subimage lying entirely with a background; (d) computing a gray scale of an image region lying contiguous to a portion of the visually approximated skin lesion boundary; (e) comparing the gray scale range for said image region with the gray scale range of each of said subimages; (f) computing the location of the skin lesion boundary in a vicinity of said image region, based upon said comparison; and (g) repeating steps (b) through (f) until an entire skin lesion boundary has been computed.

Claim 35

The method of claim 21 further comprising the step of computing a pigmentation pattern of said skin lesion.

Claim 36

The method of claim 30 wherein the steps of computing the pigmentation pattern of said skin lesion comprises: (a) computing a first order histogram, denoted by H(y i ,d); (b) computing a second order histogram, denoted by H(y i ,y j ,d); (c) analyzing said first order histogram to find peaks; (d) analyzing the second order histogram to determine peaks; (e) computing a histogram entropy, denoted by E, where: ##EQU11## (f) computing a histogram inertia measure, denoted by IM, where: ##EQU12## (g) computing a degree of correlation, denoted by C, where: ##EQU13## (h) inputting data computed on steps (c) through (g) above, into a knowledge-based system containing skin lesion probabilistic models; and (i) analyzing data stored in said knowledge-based system to determine the skin lesion pigmentation pattern.

Claim 37

The method of claim 30 further comprising the steps of: (a) storing computed skin lesion characteristics in a knowledge-based system; and (b) analyzing the skin lesion characteristics stored in said knowledge-based system to obtain a skin lesion diagnosis.

Claim 38

The method of claim 32 further comprising the steps of: (a) storing the skin lesion characteristics in a knowledge-based system containing skin lesion prognostic probabilistic models; and (b) analyzing the skin lesion characteristics stored in said knowledge-based system to obtain a prognosis of the skin lesion.