Your browser doesn't support javascript.
loading
Variability in mitotic figures in serial sections of thin melanomas.
Knezevich, Stevan R; Barnhill, Raymond L; Elder, David E; Piepkorn, Michael W; Reisch, Lisa M; Pocobelli, Gaia; Carney, Patricia A; Elmore, Joann G.
Affiliation
  • Knezevich SR; Veterans Affairs Medical Center, Seattle, Washington; Department of Pathology, University of Washington School of Medicine, Seattle, Washington. Electronic address: stevanrk@gmail.com.
  • Barnhill RL; Department of Pathology, University of California at Los Angeles, Los Angeles, California.
  • Elder DE; Department of Pathology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Piepkorn MW; Division of Dermatology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington; Dermatopathology Northwest, Bellevue, Washington.
  • Reisch LM; Department of Internal Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Pocobelli G; Department of Internal Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Carney PA; Departments of Family Medicine and Public Health and Preventive Medicine, Oregon Health and Sciences University, Portland, Oregon.
  • Elmore JG; Department of Internal Medicine, University of Washington School of Medicine, Seattle, Washington.
J Am Acad Dermatol ; 71(6): 1204-11, 2014 Dec.
Article in En | MEDLINE | ID: mdl-25239732
ABSTRACT

BACKGROUND:

T1 melanoma staging is significantly affected by tissue sampling approaches, which have not been well characterized.

OBJECTIVE:

We sought to characterize presence of mitotic figures across a minimum of 5 sequential sections of T1 melanomas.

METHODS:

A cohort of T1 melanomas with either 5 (single section per slide) or 10 (2 sections per slide) sequential sections (5-µm thickness) per case were prepared and examined for mitotic figures.

RESULTS:

In all, 44 of 82 T1 melanomas (54%) were classified as T1b. The number of sections with a mitotic figure present ranged from only 1 of 5 sections (n = 5 of 44 cases, 11.4%) to all 5 (n = 20 of 44 cases, 45.5%). A sequential approach versus a nonsequential approach did not appear to matter.

LIMITATION:

Cases were taken from a single pathology practice in the Pacific Northwest, which may not generalize to other populations in the United States.

CONCLUSION:

The variation in the presence of mitotic figures within sequential sections supports reviewing 3 to 5 sections to fulfill American Joint Committee on Cancer recommendations. The prognostic significance of a T1b melanoma with a rare mitotic figure on a single section versus a T1b melanoma with mitotic figures on multiple sections deserves more attention to see if further subclassification is possible or even necessary.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Melanoma / Mitotic Index Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Am Acad Dermatol Year: 2014 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / Melanoma / Mitotic Index Type of study: Diagnostic_studies / Guideline / Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Am Acad Dermatol Year: 2014 Type: Article