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Correspondence |

Why the First Step Should Be Abandoned!—Reply

Ashfaq A. Marghoob, MD; Ralph P. Braun, MD
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Copyright 2010 American Medical Association. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to Government Use.

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Arch Dermatol. 2010;146(10):1183-1183. doi:10.1001/archdermatol.2010.272
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Differences in cognitive processes, personal biases, and experiences probably shape differing views regarding the choice of dermoscopy algorithm preferred by any given individual. It is important to stress that despite the differing opinions being debated here, the treatment decisions, based on dermoscopic evaluations performed by physicians proficient in dermoscopy, remain the same regardless of the dermoscopic evaluation method used. With that being said, we will attempt to address some points raised by Kittler.

It is highly improbable for any dermoscopic algorithm to be without exceptions. Excluding dermatofibromas, we are aware of a few exceptions to the 2-step dermoscopy algorithm.1 2

Regarding the classification of lesions as melanocytic or nonmelanocytic, Kittler states that ink-spot lentigines are being incorrectly classified as melanocytic lesions via the 2-step algorithm. Although some ink-spot lentigines may be variants of solar lentigines (nonmelanocytic), others are variants of lentigo simplex (melanocytic).3 In the latter case, the first step of the 2-step algorithm is in fact classifying these lesions correctly.

It is important to stress that the issues being raised by Kittler pertain to the precision of the clinical diagnosis, which may or may not have any bearing on ultimate treatment. Although we should not stop striving toward clinical perfection, one should not lose sight of the ultimate aim, which is to perform a biopsy on all malignant neoplasms regardless of the leading clinical diagnosis.

Kittler highlights that in the occasional cases of pigmented Bowen disease lesions manifesting irregular dots and BCCs revealing streaks, there may result the incorrect classification of these lesions as melanocytic via the 2-step algorithm. However, both of these findings will result in melanoma entering the differential diagnosis, hence leading to a biopsy.

Even these examples are uncommon, since clinicians rely on more than dermoscopic morphologic traits in rendering a clinical diagnosis.4 The clinical features such as texture, consistency, and presence or absence of surface scale are all used in combination before a clinical diagnosis is rendered. For example, it is the concordance between the clinical features and the dermoscopic structures that help clinicians correctly identify lesions such as dermatofibromas. Furthermore, any given dermoscopic structure is not normally viewed in isolation but within the context of the other dermoscopic structures and clinical features present. In addition, knowledge of histopathology helps clinicians make sense of certain dermoscopic structures encountered in specific lesions. This places each structure in correct context, prevents misclassification of melanocytic and nonmelanocytic lesions, and assists in identifying collision tumors.

From our clinical, research, and teaching experiences, we believe that the 2-step algorithm is practical and reliable and easy to learn and apply. We acknowledge that multiple other “reliable” methods are at our disposal to evaluate lesions dermoscopically, including Kittler's pattern analysis approach.5 We agree completely with Kittler that all of these opinions need to be subjected to formal testing, some of which is in fact already under way through a study conducted by the International Dermoscopy Society. We remain optimistic that the results of this and other studies will further clarify this matter.

AUTHOR INFORMATION

Correspondence: Dr Marghoob, Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, 800 Veterans Memorial Hwy, Hauppauge, NY 11788 (marghooa@MSKCC.org).

REFERENCES

Scope  A, Benvenuto-Andrade  C, Agero  AL, Marghoob  AA. Nonmelanocytic lesions defying the two-step dermoscopy algorithm. Dermatol Surg 2006;32 (11) 1398- 1406
PubMed
Braun  RP, Rabinovitz  HS, Krischer  J.  et al.  Dermoscopy of pigmented seborrheic keratosis: a morphological study. Arch Dermatol 2002;138 (12) 1556- 1560
PubMed
Bolognia  JL. Reticulated black solar lentigo (“ink spot” lentigo). Arch Dermatol 1992;128 (7) 934- 940
PubMed
Marghoob  AA, Scope  A. The complexity of diagnosing melanoma. J Invest Dermatol 2009;129 (1) 11- 13
PubMed
Argenziano  G, Soyer  HP, Chimenti  S.  et al.  Dermoscopy of pigmented skin lesions: results of a consensus meeting via the Internet. J Am Acad Dermatol 2003;48 (5) 679- 693
PubMed

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Scope  A, Benvenuto-Andrade  C, Agero  AL, Marghoob  AA. Nonmelanocytic lesions defying the two-step dermoscopy algorithm. Dermatol Surg 2006;32 (11) 1398- 1406
PubMed
Braun  RP, Rabinovitz  HS, Krischer  J.  et al.  Dermoscopy of pigmented seborrheic keratosis: a morphological study. Arch Dermatol 2002;138 (12) 1556- 1560
PubMed
Bolognia  JL. Reticulated black solar lentigo (“ink spot” lentigo). Arch Dermatol 1992;128 (7) 934- 940
PubMed
Marghoob  AA, Scope  A. The complexity of diagnosing melanoma. J Invest Dermatol 2009;129 (1) 11- 13
PubMed
Argenziano  G, Soyer  HP, Chimenti  S.  et al.  Dermoscopy of pigmented skin lesions: results of a consensus meeting via the Internet. J Am Acad Dermatol 2003;48 (5) 679- 693
PubMed

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