Diagnostic Biopsy via In-Office Frozen Sections for Clinical Nonmelanoma Skin Cancer.


Journal

Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
ISSN: 1524-4725
Titre abrégé: Dermatol Surg
Pays: United States
ID NLM: 9504371

Informations de publication

Date de publication:
01 02 2021
Historique:
pubmed: 11 2 2021
medline: 27 4 2021
entrez: 10 2 2021
Statut: ppublish

Résumé

Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited. To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC. Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic. Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision. In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.

Sections du résumé

BACKGROUND
Treatment of nonmelanoma skin cancer (NMSC) by Mohs surgery has traditionally relied on previous pathologic evaluation of paraffin-embedded tissue. Tissue processing by frozen sections allows for expedited diagnosis and treatment; however, data on its accuracy are limited.
OBJECTIVE
To measure the accuracy and outcomes of biopsy via frozen sections for clinical NMSC.
METHODS
Biopsies of clinical NMSCs processed via frozen sections with in-office diagnosis rendered by one Mohs surgeon were retrospectively reviewed by one board-certified dermatopathologist. Discordant diagnoses were re-read in blinded fashion by both physicians. If still discordant, final diagnosis was determined by consensus discussion. Inter-rater reliability was calculated using Cohen's kappa statistic.
RESULTS
Two hundred ninety-seven lesions from 208 patients were included. Correlation between in-office and final diagnosis was 0.876 indicating "almost perfect" concordance. Sensitivity and specificity of in-office diagnosis for detecting malignancy were 98.1% and 94.4%. Seven cases (2.0%) had a clinically relevant change in final diagnosis, but appropriate treatment had been rendered. Two benign lesions (0.7%) initially diagnosed as malignant underwent excision.
CONCLUSION
In-office biopsy via frozen sections is highly accurate in confirming NMSC. This practice may speed diagnosis and treatment thus improving outcomes and patient satisfaction.

Identifiants

pubmed: 33565773
doi: 10.1097/DSS.0000000000002473
pii: 00042728-202102000-00008
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

194-199

Informations de copyright

Copyright © 2020 by the American Society for Dermatologic Surgery, Inc. Published by Wolters Kluwer Health, Inc. All rights reserved.

Références

Rogers HW, Weinstock MA, Feldman SR, Coldiron BM. Incidence estimate of nonmelanoma skin cancer (keratinocyte carcinomas) in the U.S. Population, 2012. JAMA Dermatol 2015;151:1081–6.
Bichakjian CK, Olencki T, Aasi SZ, Alam M, et al. Basal Cell Skin Cancer, Version 1.2016, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw 2016;14:574–97.
Muzic JG, Schmitt AR, Wright AC, Alniemi DT, et al. Incidence and trends of basal cell carcinoma and cutaneous squamous cell carcinoma: a population-based study in Olmsted County, Minnesota, 2000 to 2010. Mayo Clin Proc 2017;92:890–8.
Mohs F. Chemosurgery: a microscopically controlled method of cancer excision. Arch Surg 1941;42:279–95.
Tromovitch TA, Stegman SJ. Microscopie-controlled excision of cutaneous tumors: chemosurgery, fresh tissue technique. Cancer 1978;41:653–8.
Grabski WJ, Salasche SJ, McCollough ML, Berkland ME, et al. Interpretation of Mohs micrographic frozen sections: a peer review comparison study. J Am Acad Dermatol 1989;20:670–4.
Highsmith JT, Highsmith MJ, Monheit GD. Histologic accuracy of Mohs micrographic surgery. Dermatol Surg 2018;44:350–3.
Mariwalla K, Aasi SZ, Glusac EJ, Leffell DJ. Mohs micrographic surgery histopathology concordance. J Am Acad Dermatol 2009;60:94–8.
Semkova K, Mallipeddi R, Robson A, Palamaras I. Mohs micrographic surgery concordance between Mohs surgeons and dermatopathologists. Dermatol Surg 2013;39:1648–52.
Dinehart MS, Coldiron BM, Hiatt K, Breau RL. Concordance of frozen and permanent sections for the diagnosis of skin lesions. Dermatol Surg 2010;36:1111–5.
Onajin O, Wetter DA, Roenigk RK, Gibson LE, et al. Frozen section diagnosis for non-melanoma skin cancers: correlation with permanent section diagnosis. J Cutan Pathol 2015;42:459–64.
Machan M, Zitelli J, Brodland D. Effectiveness and advantages of on-site pathology services in the care of patients with nonmelanoma skin cancer. Dermatol Surg 2016;42:77–82.
Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics 1977;33:159–74.
Elmore JG, Barnhill RL, Elder DE, Longton GM, et al. Pathologists' diagnosis of invasive melanoma and melanocytic proliferations: observer accuracy and reproducibility study. BMJ 2017;357:j2813.
Davis DA, Donahue JP, Bost JE, Horn TD. The diagnostic concordance of actinic keratosis and squamous cell carcinoma. J Cutan Pathol 2005;32:546–51.
Jagdeo J, Weinstock MA, Piepkorn M, Bingham SF. Department of veteran affairs topical tretinoin chemoprevention trial group. Reliability of the histopathologic diagnosis of keratinocyte carcinomas. J Am Acad Dermatol 2007;57:279–84.
Leader NF, Means AD, Robinson-Bostom L, Telang GH, et al. Interrater reliability for histopathologic diagnosis of keratinocyte carcinomas. J Am Acad Dermatol 2018;78:185–7.
Wechsler J, Zanetti R, Schrameck C, Rosso S, et al. Reproducibility of histopathologic diagnosis and classification of non-melanocytic skin cancer: a panel exercise in the framework of the multicenter southern European study HELIOS. Tumori 2001;87:95–100.
Konda S, Francis J, Motaparthi K, Grant-Kels JM; Group for Research of Corporatization and Private Equity in Dermatology. Future considerations for clinical dermatology in the setting of 21st century American policy reform: corporatization and the rise of private equity in dermatology. J Am Acad Dermatol 2019;81:287–296.e8.
Drew BA, Karia PS, Mora AN, Liang CA, et al. Treatment patterns, outcomes, and patient satisfaction of primary epidermally limited nonmelanoma skin cancer. Dermatol Surg 2017;43:1423–30.

Auteurs

Patrick M Mulvaney (PM)

All authors are affiliated with the Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH