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Observation of Chrysalis Structures With Polarized Dermoscopy

Ashfaq A. Marghoob, MD; Lester Cowell, MBBS, ACCAM; Alfred W. Kopf, MD; Alon Scope, MD
[+] Author Affiliations

James M. Grichnik, MD, PhD

Ashfaq A. Marghoob, MD
Alon Scope, MD

Copyright 2009 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.

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Arch Dermatol. 2009;145(5):618-618. doi:10.1001/archdermatol.2009.28
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Collagen bundles have birefringent properties that cause a rapid randomization of polarized light, explaining why collagen is more conspicuous under polarized dermoscopy.1 Skin lesions with an increased amount of collagen will often reveal shiny, bright white, orthogonal linear streaks, which we have termed “chrysalis structures.” These structures are not apparent to the unaided eye nor are they visible with nonpolarized dermoscopy. The most obvious examples of lesions that display chrysalis structures are dermatofibromas (Figure 1)2 3 and scars. In basal cell carcinoma, chrysalis structures are often observed, probably owing to the associated fibroplasia (Figure 2).4 5 In addition, chrysalis structures are seen on occasion in Spitz nevi (Figure 3 [courtesy of Harold Rabinovitz, MD, Skin and Cancer Associates, Plantation, Florida]) and in melanoma (Figure 4), probably corresponding to changes in the composition and orientation of collagen in the stroma that underlies these melanocytic neoplasms.6 8 Interestingly, it has been suggested that collagen remodeling in the stroma of melanoma is important for the invasion of tumor cells into the dermis.9

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Figure 2.

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Figure 3.

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Figure 4.

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Polarized dermoscopy can also be used in a dynamic fashion. Rotating the polarized dermoscope while keeping the eye (or attached camera) stationary will cause the chrysalis structures to appear more or less prominent depending on the angle of polarization (a video is here). This phenomenon is called angular dependence of polarized light and probably reflects the nonrandom orientation of collagen in the dermis. Dynamic polarized dermoscopy is a simple optical maneuver to validate the presence of chrysalis structures in lesions.

REFERENCES

Pan  Y, Gareau  DS, Scope  A, Rajadhyaksha  M, Mullani  NA, Marghoob  AA. Polarized and nonpolarized dermoscopy: the explanation for the observed differences. Arch Dermatol 2008;144 (6) 828- 829
PubMed
Agero  AL, Taliercio  S, Dusza  SW, Salaro  C, Chu  P, Marghoob  AA. Conventional and polarized dermoscopy features of dermatofibroma. Arch Dermatol 2006;142 (11) 1431- 1437
PubMed
Zaballos  P, Puig  S, Llambrich  A, Malvehy  J. Dermoscopy of dermatofibromas: a prospective morphological study of 412 cases. Arch Dermatol 2008;144 (1) 75- 83
PubMed
Giacomel  J, Zalaudek  I. Dermoscopy of superficial basal cell carcinoma. Dermatol Surg 2005;31 (12) 1710- 1713
PubMed
Benvenuto-Andrade  C, Dusza  SW, Agero  AL. Differences between polarized light dermoscopy and immersion contact dermoscopy for the evaluation of skin lesions. Arch Dermatol 2007;143 (3) 329- 338
PubMed
Kääriäinen  E, Nummela  P, Soikkeli  J. Switch to an invasive growth phase in melanoma is associated with tenascin-C, fibronectin, and procollagen-I forming specific channel structures for invasion. J Pathol 2006;210 (2) 181- 191
PubMed
van Kempen  LC, van Muijen  GN, Ruiter  DJ. Melanoma progression in a changing environment. Eur J Cell Biol 2007;86 (2) 65- 67
PubMed
van Kempen  LC, van Muijen  GN, Ruiter  DJ. Stromal responses in human primary melanoma of the skin. Front Biosci 2005;102922- 2931
PubMed
van Kempen  LC, Rijntjes  J, Mamor-Cornelissen  I. Type I collagen expression contributes to angiogenesis and the development of deeply invasive cutaneous melanoma. Int J Cancer 2008;122 (5) 1019- 1029
PubMed

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Figure 1.

Grahic Jump Location
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Figure 2.

Grahic Jump Location
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Figure 3.

Grahic Jump Location
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Figure 4.

Grahic Jump Location

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Pan  Y, Gareau  DS, Scope  A, Rajadhyaksha  M, Mullani  NA, Marghoob  AA. Polarized and nonpolarized dermoscopy: the explanation for the observed differences. Arch Dermatol 2008;144 (6) 828- 829
PubMed
Agero  AL, Taliercio  S, Dusza  SW, Salaro  C, Chu  P, Marghoob  AA. Conventional and polarized dermoscopy features of dermatofibroma. Arch Dermatol 2006;142 (11) 1431- 1437
PubMed
Zaballos  P, Puig  S, Llambrich  A, Malvehy  J. Dermoscopy of dermatofibromas: a prospective morphological study of 412 cases. Arch Dermatol 2008;144 (1) 75- 83
PubMed
Giacomel  J, Zalaudek  I. Dermoscopy of superficial basal cell carcinoma. Dermatol Surg 2005;31 (12) 1710- 1713
PubMed
Benvenuto-Andrade  C, Dusza  SW, Agero  AL. Differences between polarized light dermoscopy and immersion contact dermoscopy for the evaluation of skin lesions. Arch Dermatol 2007;143 (3) 329- 338
PubMed
Kääriäinen  E, Nummela  P, Soikkeli  J. Switch to an invasive growth phase in melanoma is associated with tenascin-C, fibronectin, and procollagen-I forming specific channel structures for invasion. J Pathol 2006;210 (2) 181- 191
PubMed
van Kempen  LC, van Muijen  GN, Ruiter  DJ. Melanoma progression in a changing environment. Eur J Cell Biol 2007;86 (2) 65- 67
PubMed
van Kempen  LC, van Muijen  GN, Ruiter  DJ. Stromal responses in human primary melanoma of the skin. Front Biosci 2005;102922- 2931
PubMed
van Kempen  LC, Rijntjes  J, Mamor-Cornelissen  I. Type I collagen expression contributes to angiogenesis and the development of deeply invasive cutaneous melanoma. Int J Cancer 2008;122 (5) 1019- 1029
PubMed

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