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Correspondence |

Inadequate Biopsy Technique and Specimen Size: An Alarming Trend That Compromises Patient Care and an Appeal to Our Clinical Colleagues

Klaus Sellheyer, MD; Paula Nelson, MD; Wilma F. Bergfeld, 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):1180-1181. doi:10.1001/archdermatol.2010.293
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With changes in the delivery of health care in America looming, dermatologists may increase the number of patients they see per time unit and biopsies they perform in an attempt to balance declining reimbursement rates. In addition, roughly one-third of dermatologists employ physician extenders.1 While this is often done with the explanation of a shortage of dermatologists, it may be also motivated by the desire to increase revenues.

In 2005, Fernandez et al2 documented a trend toward smaller skin biopsy specimens over a period of 15 years (1988 to 2003) and concluded that a “definitive diagnosis may become increasingly difficult as the size of the biopsy specimens continues to get smaller.”2 (p339) It is not only the size of the specimen but also the type of biopsy that affects the histopathologic interpretation. This was most recently documented in a study3 published in the March 2010 issue of the Archives of Dermatology, which implied that punch and shave biopsies of melanoma lesions led to a higher risk of histopathologic misdiagnosis.

The Figure depicts only 5 examples of too-small or inadequately sampled specimens, among them a curetted melanoma, a shave biopsy extending only into the midepidermis to rule out basal cell carcinoma, and a shave biopsy to rule out alopecia areata. Although these examples vary between different practices, many dermatologists and physician extenders submit these types of inadequate specimens for histopathologic diagnosis. The examples document a trend, already suspected to be influenced by pressure to see more patients, in which dermatologists choose faster biopsy techniques such as shave, curettage, or 2-mm punch biopsies.2 When Kopf and Popkin4 initially popularized the use of the shave biopsy technique in dermatology in 1974, they certainly did not have in mind shaved specimens that barely scratch the skin surface. While aesthetic outcomes may be used as an argument, economic forces may play a larger role in the biopsy technique chosen.

Place holder to copy figure label and caption
Figure

Various biopsy specimens are depicted showing inadequate technique and/or specimen size submitted by health care providers to our dermatopathology practice for evaluation. A-C, Superficial curettage specimen of melanoma. The arrow in A points to the area shown at higher magnification in B; C represents the accompanying melan-a stain. D, Superficial curettage specimen obtained to rule out chondrodermatitis nodularis helicis. Only the superficial papillary dermis was sampled and is present focally only. The typical architectural features of the disease cannot be evaluated, thus precluding a definitive diagnosis. E, This 2-mm punch biopsy specimen extends into the upper reticular dermis only. It was performed to rule out a folliculitis. Despite step sections through the block, a hair follicle was not noted. F, This superficial shave biopsy specimen extends into the midepidermis only, despite step sections. The intended purpose of the biopsy, to rule out basal cell carcinoma, could not be achieved by histopathologic examination. G, This shave biopsy specimen of the scalp was submitted to rule out alopecia areata. Specimens A, D, and F were obtained by board-certified dermatologists; E and G, by physician assistants. Hematoxylin-eosin was used in all specimens except panel C, for which melan-a was used; original magnifications for panels A, B, C, D, E, F, and G were ×12.5, ×200, ×200, ×50, ×50, ×25, and ×25, respectively.

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Furthermore, lack of appropriate supervision of physician extenders can affect the patient care they provide, including their choice of biopsy technique and consequent too-small skin specimens for a reliable histopathologic diagnosis. As pointed out in the editorial published simultaneously with the study by Ng et al,3 “biopsy technique, per se, does not increase disease-specific mortality,”5 (p325) but it certainly increases the risk of histopathologic misdiagnosis. The dermatologist's duties can be delegated to physician assistants or nurse practitioners, but liability or responsibility cannot.6 7

We have to critically ask ourselves the following questions: How much are we willing to compromise biopsy size? And are we—as clinicians—truly aware of what we submit to the dermatopathologist and what effect our biopsy technique has on patient care? Or, to pose it more pointedly, are we practicing medicine to the highest ethical standards, if we submit biopsy specimens inadequate for histopathologic diagnosis? With America's health care system under critical review, we appeal to our clinical colleagues to seriously consider adequate sample size and biopsy technique to deliver the most accurate histopathologic diagnosis and result in the best patient care.

AUTHOR INFORMATION

Correspondence: Dr Sellheyer, Nelson Dermatopathology Associates, 5775 Dupree Dr NW, Atlanta, GA 30327 (klaus.sellheyer@gmail.com).

Financial Disclosure: None reported.

REFERENCES

Resneck  JS  Jr, Kimball  AB. Who else is providing care in dermatology practices? trends in the use of nonphysician clinicians. J Am Acad Dermatol 2008;58 (2) 211- 216
PubMed
Fernandez  EM, Helm  T, Ioffreda  M, Helm  KF. The vanishing biopsy: the trend toward smaller specimens. Cutis 2005;76 (5) 335- 339
PubMed
Ng  JC, Swain  S, Dowling  JP, Wolfe  R, Simpson  P, Kelly  JW. The impact of partial biopsy on histopathologic diagnosis of cutaneous melanoma: experience of an Australian tertiary referral service. Arch Dermatol 2010;146 (3) 234- 239
PubMed
Kopf  AW, Popkin  GL. Letter: shave biopsies for cutaneous lesions. Arch Dermatol 1974;110 (4) 637
PubMed
Marghoob  AA, Terushkin  V, Dusza  SW, Busam  K, Scope  A. Dermatologists, general practitioners, and the best method to biopsy suspect melanocytic neoplasms. Arch Dermatol 2010;146 (3) 325- 328
PubMed
Mamelak  AJ, Goldberg  LH. Dermatology physician extenders: a new risk factor? J Am Acad Dermatol 2008;59 (5) 897
PubMed
Nestor  MS. The use of mid-level providers in dermatology: a liability risk? Semin Cutan Med Surg 2005;24 (3) 148- 151
PubMed

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Figures

Place holder to copy figure label and caption
Figure

Various biopsy specimens are depicted showing inadequate technique and/or specimen size submitted by health care providers to our dermatopathology practice for evaluation. A-C, Superficial curettage specimen of melanoma. The arrow in A points to the area shown at higher magnification in B; C represents the accompanying melan-a stain. D, Superficial curettage specimen obtained to rule out chondrodermatitis nodularis helicis. Only the superficial papillary dermis was sampled and is present focally only. The typical architectural features of the disease cannot be evaluated, thus precluding a definitive diagnosis. E, This 2-mm punch biopsy specimen extends into the upper reticular dermis only. It was performed to rule out a folliculitis. Despite step sections through the block, a hair follicle was not noted. F, This superficial shave biopsy specimen extends into the midepidermis only, despite step sections. The intended purpose of the biopsy, to rule out basal cell carcinoma, could not be achieved by histopathologic examination. G, This shave biopsy specimen of the scalp was submitted to rule out alopecia areata. Specimens A, D, and F were obtained by board-certified dermatologists; E and G, by physician assistants. Hematoxylin-eosin was used in all specimens except panel C, for which melan-a was used; original magnifications for panels A, B, C, D, E, F, and G were ×12.5, ×200, ×200, ×50, ×50, ×25, and ×25, respectively.

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Resneck  JS  Jr, Kimball  AB. Who else is providing care in dermatology practices? trends in the use of nonphysician clinicians. J Am Acad Dermatol 2008;58 (2) 211- 216
PubMed
Fernandez  EM, Helm  T, Ioffreda  M, Helm  KF. The vanishing biopsy: the trend toward smaller specimens. Cutis 2005;76 (5) 335- 339
PubMed
Ng  JC, Swain  S, Dowling  JP, Wolfe  R, Simpson  P, Kelly  JW. The impact of partial biopsy on histopathologic diagnosis of cutaneous melanoma: experience of an Australian tertiary referral service. Arch Dermatol 2010;146 (3) 234- 239
PubMed
Kopf  AW, Popkin  GL. Letter: shave biopsies for cutaneous lesions. Arch Dermatol 1974;110 (4) 637
PubMed
Marghoob  AA, Terushkin  V, Dusza  SW, Busam  K, Scope  A. Dermatologists, general practitioners, and the best method to biopsy suspect melanocytic neoplasms. Arch Dermatol 2010;146 (3) 325- 328
PubMed
Mamelak  AJ, Goldberg  LH. Dermatology physician extenders: a new risk factor? J Am Acad Dermatol 2008;59 (5) 897
PubMed
Nestor  MS. The use of mid-level providers in dermatology: a liability risk? Semin Cutan Med Surg 2005;24 (3) 148- 151
PubMed

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