Erich M. Gaertner. 1. Introduction. 3. Results. 2. Material and Methods

Similar documents
Actinic keratosis (AK): Dr Sarma s simple guide

Basal cell carcinoma 5/28/2011

Epidermolytic hyperkeratosis and acantholytic dyskeratosis. Porokeratoma ORIGINAL ARTICLE

Case Report A Rare Cutaneous Adnexal Tumor: Malignant Proliferating Trichilemmal Tumor

Pathology of the skin. Dr Fónyad László, 1sz. Patológiai és Kísérleti Rákkutató Intézet, SE

Case Report Clear Cell Basal Cell Carcinoma

Benign and malignant epithelial lesions: Seborrheic keratosis: A common benign pigmented epidermal tumor occur in middle-aged or older persons more

NEOPLASMS OF THE SURFACE EPITHELIUM (KERATINOCYTES)

Benign Lichenoid Keratosis

المركب النموذج--- سبيتز وحمة = Type Spitz's Nevus, Compound SPITZ NEVUS 1 / 7

Benign versus Cancerous Lesions How to tell the difference FMF 2014 Christie Freeman MD, CCFP, DipPDerm, MSc

Chapter 6 Squamous Cell Carcinoma: Variants and Challenges

Histopathology: skin pathology

Simulators of melanoma

IT S FUNDAMENTAL MY DEAR WATSON! A SHERLOCKIAN APPROACH TO DERMATOLOGY

Dermoscopy: Recognizing Top Five Common In- Office Diagnoses

ISPUB.COM. Seborrheic Keratosis: A Pictorial Review of the Histopathologic Variations. D Sarma, S Repertinger

MECHANISMS OF HUMAN DISEASE: LABORATORY SESSION PATHOLOGY OF THE SKIN LAB. Friday, February 13, :30 am 11:00 am

A dinical and histopathologic entity associated with an increased risk of nonmelanoma skin cancer

LUMPS AND BUMPS: AN ORGANIZED APPROACH TO DIAGNOSIS AND MANAGEMENT

Table of Contents: Part 1 Medical Dermatology. Chapter 1 Acneiform Disorders. Acne. Acne Vulgaris. Pomade Acne. Steroid Acne

Dermatologists and subspecialty dermatopathologists,

Pathology of the skin. 2nd Department of Pathology, Semmelweis University

MECHANISMS OF HUMAN DISEASE: LABORATORY SESSION PATHOLOGY OF THE SKIN LAB. Friday, February 12, :30 am 11:00 am

Self assesment Case 21

Clinical characteristics

CONDITIONS OF THE SKIN

Case Report A Case of Cystic Basal Cell Carcinoma Which Shows a Homogenous Blue/Black Area under Dermatoscopy

Case Report Micromelanomas: A Review of Melanomas 2mmand a Case Report

Dermatopathology: The tumor is composed of keratinocytes which show atypia, increase mitoses and abnormal mitoses.

Supplementary Online Content

Objectives. 1. Recognizing benign skin lesions. 2.Know which patients will likely need surgical intervention.

DESCRIPTIONS FOR MED 3 ROTATIONS Dermatology A3S

Malignant tumors of melanocytes: Part 1. Deba P Sarma, MD., Omaha

Important Decisions in Dermatopathology: The Clinico- Pathologic Correlation. Dermatopathology Specialists Needed. Changing Trends

Dermatology for the PCP Deanna G. Brown, MD, FAAD Susong Dermatology Consulting Staff at CHI Memorial

Systemic epidermal nevus with involvement of the oral mucosa due to FGFR3 mutation

Malignant non-melanocytic lesions

LENTIGO SIMPLEX. Epidemiology

Lid Lesions: Relax or Refer

Department of Dermatology, Nippon Medical School, 1-1-5, Sendagi, Bunkyo-ku, Tokyo , Japan 2

Lichenoid Tissue Reaction in Malignant Melanoma A Potential Diagnostic Pitfall

Disseminated epidermolytic acanthoma probably related to trauma

W. Kempf ] M. Hantschke ] H. Kutzner ] W. H.C. Burgdorf. Dermatopathology

Eruptive Tumors of the Follicular Infundibulum: An Unexpected Diagnosis of Hypopigmented Macules

Some of the most important metabolic QUANTITATIVE STUDIES OF EPIDERMAL SULFHYDRYL*

Case Report Multiple Giant Cell Tumors of Tendon Sheath Found within a Single Digit of a 9-Year-Old

Associate Clinical Professor of Dermatology MUSC

Disorders of the vulva

Dermatological Manifestations in the Elderly. Sanjay Siddha Staff Dermatologist UHN & MSH

Skin lesions The Good and the Bad. Dr Virginia Hubbard Ipswich Hospital NHS Trust Barts and the London School of Medicine and Dentistry

Lumps and Bumps: The Dermatology of Lid Lesions

Desmoplastic Melanoma R/O BCC. Clinical Information. 74 y.o. man with lesion on left side of neck r/o BCC

Identifying Skin Cancer. Mary S. Stone MD Professor of Dermatology and Pathology University of Iowa Carver College of Medicine March, 2018

Clinical and Histopathological Investigation of Seborrheic Keratosis

A Clinicopathological study of skin and adnexal neoplasms at a rural based tertiary teaching hospital

Porokeratosis: Introduction

Case Report Features of the Atrophic Corpus Mucosa in Three Cases of Autoimmune Gastritis Revealed by Magnifying Endoscopy

Case Report Five-Year Survival after Surgery for Invasive Micropapillary Carcinoma of the Stomach

Learning Objectives. Tanning. The Skin. Classic Features. Sun Reactive Skin Type Classification. Skin Cancers: Preventing, Screening and Treating

Keratinocyte tumors. Actinic Keratosis. Squamous cell carcinoma in situ. Squamous Cell Carcinoma. (aka Bowen s disease)

Clinically Microscopically Pathogenesis: autoimmune not lifetime

Pigmented skin lesions: are they all of melanocytic origin? A histopathological perspective

Samer Ghosn, MD Associate professor, Derpartment of Dermatology American University of Beirut Medical Center. Follicular lesions

Pathology. Skin Tumor. Bayan N. Mohammad 15/10/2015. Mohammad al-orjani. Page 0 of 23

EARLY ONLINE RELEASE

Case Report Denosumab Chemotherapy for Recurrent Giant-Cell Tumor of Bone: A Case Report of Neoadjuvant Use Enabling Complete Surgical Resection

Squamous papilloma Squamous acanthoma Keratoacanthoma Verruca vulgaris Condyloma acuminatum Focal epithelial hyperplasia Sino nasal papilloma

Clinical Policy: Benign Skin Lesion Removal Reference Number: CP.MP.HN150

Clinical Differential Diagnosis 4/16/2018 DERMATOPATHOLOGY OF THE GENITALIA AND BREAST NO CONFLICTS TO DISCLOSE

R. F. Falkenstern-Ge, 1 S. Bode-Erdmann, 2 G. Ott, 2 M. Wohlleber, 1 and M. Kohlhäufl Introduction. 2. Histology

Grover s disease: A case report.

Basics in Dermoscopy

04/09/2018. Squamous Cell Neoplasia and Precursor Lesions. Agenda. Squamous Dysplasia. Squamo-proliferative lesions. Architectural features

Common skin tumors. Benign Epidermal Tumors. Topic. Clinicopathologic Variants. Seborrheic keratoses

Mucinoses Diverse group of disorders which have in common deposition of basophilic, finely granular and stringy material in the connective tissues of

Clinical Study Treatment of Mesh Skin Grafted Scars Using a Plasma Skin Regeneration System

Integumentary system pertains to the skin, subcutaneous tissue and areolar tissue.

Squamous Cell Neoplasia and Precursor Lesions

Rash Decisions Approach to the patient with a skin condition

Melanocytes in nonlesional sun-exposed skin: A multicenter comparative study

Contents. 3 Diagnostic Tests and Studies Introduction Examination... 27

Doctors of Optometry Course Notes

Non-Melanocytic Pattern Dermoscopy

Diploma examination. Dermatopathology: First paper. Tuesday 21 March Candidates must answer FOUR questions ONLY. Time allowed: Three hours

UNIVERSITY OF MEDICINE AND PHARMACY OF CRAIOVA FACULTY OF MEDICINE DOCTORAL THESIS SUMMARY

Case Report Nevus Lipomatosus Superficialis with a Folliculosebaceous Component: Report of 2 Cases

Non-melanocytic Patterns

Appendix D: Authorization Guidelines for Dermatology Services

Chapter 8 Skin Disorders and Diseases

Common Benign Lesions and Skin Cancers. 22nd May 2015 Dr Mark Foley

Dermatology Procedure Coding

MEDICAL POLICY Benign Skin Lesion Removal

Treatment or Removal of Benign Skin Lesions

Associate Professor Amanda Oakley. Professor H. Peter Soyer. Academic Dermatologist The University of Queensland Brisbane. Dermatologist Hamilton

Case Report Intracranial Capillary Hemangioma in the Posterior Fossa of an Adult Male

Cancer Reporting for Dermatologists. Florida Department of Health Florida Cancer Data System. March 9, Agenda

Clinical Study Mucosal Melanoma in the Head and Neck Region: Different Clinical Features and Same Outcome to Cutaneous Melanoma

Transcription:

Skin Cancer Volume 2011, Article ID 645743, 5 pages doi:10.1155/2011/645743 Research Article Incidental Cutaneous Reaction Patterns: Epidermolytic Hyperkeratosis, Acantholytic Dyskeratosis, and Hailey-Hailey-Like Acantholysis: A Potential Marker of Premalignant Skin Change Erich M. Gaertner SaraPath Diagnostics, 2001 Webber Street, Sarasota, FL 34239, USA Correspondence should be addressed to Erich M. Gaertner, dermpathdoc@msn.com Received 8 December 2010; Accepted 28 January 2011 Academic Editor: M. Lebwohl Copyright 2011 Erich M. Gaertner. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Focal acantholytic dyskeratosis (FAD), epidermolytic hyperkeratosis (EHK), and Hailey-Hailey-like acantholysis (HH) represent unique histology reaction patterns, which can be associated with defined phenotypic and genotypic alterations. Incidental microscopic foci demonstrating these patterns have been identified in skin and mucosal specimens in associationwith a gamut of disease processes. These changes, when secondary, are of unclear etiology and significance. The following study further analyzes the incidence and association of these histologic patterns in a routine pathology/dermatopathology practice. 1. Introduction A variety of incidental microscopic cutaneous changes have been described in skin and mucosal specimens. Whether these represent spurious changes of no consequence, or true manifestations of underlying cellular alterations, remains unclear. Incidental FAD, HH, and EHK have been reported in association with a wide variety of benign and malignant skin conditions. (Table 2) Some authors believe these changes represent markers for underlying widespread cellular damage, likely from prolonged sun/ultraviolet light exposure. Several studies show an association of these changes with preneoplastic lesions and malignancy, supporting this theory. However, others cite a variety of clinical and pathologic evidence to refute this. A potential association between EHK, and possibly FAD, with atypical/dysplastic nevus has also been reported, although not uniformly. 2. Material and Methods 247 consecutive skin specimens covering a three-month period (1/04-3/04) were reviewed by the author to identify incidental foci of Hailey-Hailey-like acantholysis (HH) and focal acantholytic dyskeratosis (FAD). Subsequently, 500 consecutive skin specimens were reviewed by the author (8/08-9/08) at a different institution to evaluate for incidental foci of epidermolytic hyperkeratosis (EHK). An incidental focus was defined as a minor histologic finding occurring within a biopsy or excision specimen demonstrating a separate, primary process. All cases in which these patterns comprised the primary process were excluded. HH, FAD, and EHK patterns were defined utilizing standard diagnostic criteria. (Table 1) All cases were formalin fixed, paraffin embedded, and hematoxylin and eosin stained as per standard protocol. 3. Results Six cases of incidental FAD and HH were identified in the 247 skin specimens reviewed, representing 2.4% of the total reviewed. Of the six cases, three were shave biopsies (chest, back, and face), two were excisions (back, face), and one was a punch biopsy (scalp). Three specimens had an HH-like pattern (1.2% of total), and three had an FAD pattern. Four patients were male and two were female. The average patient age was 68 years (range 41 86). Three cases

2 Skin Cancer Table 1 Diagnosis Epidermolytic hyperkeratosis Focal acantholytic dyskeratosis Hailey-Haileylike acantholysis Histology Perinuclear vacuolization of keratinocytes in the upper epidermis, irregular keratohyaline granules, and compact hyperkeratosis Acantholysis and dyskeratosis at all levels of the epidermis, suprabasalar clefting, hyperkeratosis, and parakeratosis Prominent acantholysis at all epidermal levels with epidermal hyperplasia and often suprabasal clefting were associated with malignant or premalignant epidermal neoplasia: basal cell carcinoma (HH), actinic keratosis (HH), and melanoma in situ (FAD) (Figure 3). Two were associated with significant inflammation: inflamed seborrheic keratosis (HH) and bullous lichen planus (FAD) (Figure 4). One biopsy was of lichen simplex chronicus (FAD) (Figure 2). The average diameter of acantholysis was 0.3 mm, with a range of 0.1 mm to 0.5 mm. Four cases were associated with prominent solar elastosis. Nine cases of EHK were identified in the 500 skin specimens reviewed, representing 1.8% of total. Of the nine cases, six were excisions (arm, cheek, back [9], and neck [9]), and three were shave biopsies (thigh and back [9]). Four patients were male and five were female. The average patient age was 68 years (range 54 85). Six cases were associated with excisions of epidermal malignancies: basal cell carcinoma [16], squamous cell carcinoma [9], and melanoma in situ [7]. Three cases were associated with biopsies of dysplastic/clark s nevi (out of a total of 82 dysplastic nevi diagnosed during this period) (Figure 1). The average diameter of EHK was 0.15 mm, with a range of 0.05 mm to 0.8 mm. Six cases were associated with prominent solar elastosis. None were associated with significant inflammation. 4. Discussion Several previous studies have reviewed incidental foci of FAD, HH, or EHK. In the largest studies, incidental acantholysis was identified in 14 of 9000 specimens [35], and incidental FAD was identified in 8 of 5800 skin specimens [21]. Incidental EHK was identified in 21 out of approximately 30,000 specimens [1] and 41 out of 21,176 consecutive specimens [34]. In another study, these incidental reaction patterns were identified in 2.6% of the 1606 reviewed skin specimens, with incidental FAD identified in 0.44% (7 cases), EHK in 1.2% (19 cases), and HH in 0.68% (11 cases) [20]. The reported age of affected patients ranged from 3 to 87 years, with the largest study yielding a mean age of 55 years for FAD and 45 years for EHK. (8,25) There is no reported significant sex difference for incidental FAD or HH patterns, but incidental EHK was twice as common in men than women in the largest study [1]. These foci occur in both sun-exposed and sun-protected areas, with occurrence on the trunk more common than the head/neck or extremities. The involved areas are generally Figure 1: Incidental epidermolytic hyperkeratosis occurring in association with a dysplastic junctional nevus. (200X magnification, hematoxylin, and eosin stain). Figure 2: Incidental focal acantholytic dyskeratosis occurring in a biopsy of lichen simplex chronicus. (200X magnification, hematoxylin, and eosin stain). quite small, often involving only a single rete ridge, although have been reported as large as 12 mm [21]. They generally occurred in clinically normal skin adjacent to the primary lesion although they can occur within the lesion. Occasionally, these patterns are combined in a single specimen, and foci of acantholysis with overlapping histologic patterns have been described. Other reported incidental acantholytic patterns include those with features of pemphigus vulgaris and superficial pemphigus [35] The etiology of these changes is unclear. Incidental FAD, HH, and EHK have been previously associated with premalignant and malignant lesions. This was also noted in the current study, with incidental FAD and HH showing a 50% association (3 of 6 cases), and EHK showing a 100% association (9 of 9 cases if one includes dysplastic nevus in this category). Of note, 3 of 9 cases of incidental EHK were associated with dysplastic nevus. A total of 82 dysplastic nevi were diagnosed during the study, yielding a low sensitivity of 3.7% for EHK as a marker for dysplastic nevi, although of a high specificity, given no cases were identified in ordinary nevi. Incidental EHK has been reported to be a useful marker when present for dysplastic nevus, being found more commonly in or around nevi with architectural disorder than in common melanocytic nevi [5]. This was confirmed in a

Skin Cancer 3 Table 2: Conditions reported in association with described incidental reaction patterns. Epidermal hyperkeratosis Focal acantholytic dyskeratosis Hailey-Hailey-like acantholysis Acanthoma [1], acrosyringeal epidermolytic papulosis neviformis [2], actinic keratosis [1, 3], atypical/dysplastic nevus [4 6], basal cell carcinoma [1, 3], epidermoid cyst [3], infundibular cyst [7], dilated hair follicle [4], dilated pore [8], drug-induced acne [9], epidermal nevus [1, 3], granuloma annulare [10], hair follicle [1], hidradenoma [3], intraepidermal sweat duct unit [3], junctional/compound melanocytic nevus [1, 4 6], leukoplakia [11, 12], lichen amyloidosis [10], melanoma [1, 13], nevus comedonicus [14, 15], normal oral mucosa [16], nummular eczema [3], reactive erythema [1], scar [1, 3], seborrheic keratosis [1, 10], squamous cell carcinoma [10, 17], systemic sclerosis [18], tattoo [1], trichilemmal cyst [10] Basal cell carcinoma [19], chondrodermatitis nodularis helicis [19], benign nevi [19, 20], bullous lichen planus [ ], condyloma [21, 22], lichen simplex chronicus [ ], comedone [19], dermatofibroma [19, 23], fibrous papule [24], hemorrhoids [25, 26], malignant melanoma [19, 20, 27], melanocytic nevi with architectural disorder, scars, ruptured follicle, seborrheic keratoses [4, 19, 20, 22], pityriasis rosea [28], pityriasis rubra pilaris [29 31], psoriasis [24, 28], scar [20], squamous cell carcinoma [17], trichofolliculoma [32, 33], vascular nevi/cutis marmorata telangiectasis congenita, vascular twin nevi [34] Acral arteriovenous hemangioma, psoriasis, regressing keratoacanthoma, [35], condyloma acuminatum [28], actinic keratosis [ ], basal cell carcinoma [ ], benign tumors, malignant tumors [2], seborrheic keratosis [ ] Current report. Figure 3: Incidental focal acantholytic dyskeratosis associated with prominent solar elastosis. This occurred in association with an excision of a melanoma in situ. (400X magnification, hematoxylin, and eosin stain). follow-up study [6], although the association was of limited utility, given a low sensitivity, with only 4% of atypical nevi showing incidental EHK [5]. A follow-up study however failed to identify this association but did identify one between incidental FAD and dysplastic nevi [4]. Given the frequent association of incidental FAD, HH, and EHK with neoplastic or preneoplastic lesions, some authors postulate these changes are markers of widespread mutagenic change in the skin secondary to prolonged UV exposure field cancerization [20]. Ultraviolet light exposure has been linked to other known acantholytic disorders, such as transient acantholytic dermatosis, and has been reported to affect intercellular adhesion molecules. In the current cases, the majority were associated with prominent solar elastosis, reflecting longstanding solar damage. However, most studies show no statistically increased Figure 4: Incidental focus of Hailey-Hailey-like acantholysis, occurring in association with a benign keratosis with features of seborrheic keratosis. (200X magnification, hematoxylin, and eosin stain). incidence in sun-exposed versus non-sun-exposed skin for these incidental changes. Additionally, these foci occur in clinically and microscopically normal skin and mucosa, and one published abstract-postulated incidental EHK may be a common subclinical finding, with more than 20 microscopic foci present in an individual s normal skin [34]. Significant inflammation was also identified in several current cases, and multiple published case reports associate a variety of inflammatory dermatoses with incidental acantholysis. As with solar damage, inflammation can affect intercellular adhesion in a variety of ways, to include changes in intracellular adhesion molecules and cytokine release. The defined genetic abnormalities described for HH and EHK as primary processes have not been identified in these

4 Skin Cancer incidental foci although they have not been well studied. As in previous studies, the foci of reported incidental FAD, HH, and EHK were quite small (0.3 mm for FAD/HH and 0.15 for EHK). Most of them were found in uninvolved skin adjacent to the primary lesion, but some were found within the lesion proper. Several of the primary disease processes in the current series have not been previously reported in association with incidental acantholysis (FAD and HH), such as bullous lichen planus. Incidental FAD, HH, and EHK are interesting, uncommon cutaneous changes of unclear etiology and significance. In the current paper, these foci were associated with epidermal neoplasia, solar change, and inflammation. An association with premalignant change and malignancy has been previously reported, although not uniformly. An association between dysplastic nevi and incidental EHK and FAD has also been noted and may be of limited diagnostic utility. The exact etiology of these secondary patterns is unclear, but their presence may reflect more widespread, subclinical cutaneous injury. Statement of Financial Interest No competing financial interest exists. The research received no specific grant from a funding agency in the public, commercial, or not-for-profit sectors. References [1] P. Mahaisavariya, P. R. Cohen, and R. P. Rapini, Incidental epidermolytic hyperkeratosis, American Dermatopathology, vol. 17, no. 1, pp. 23 28, 1995. [2] A. M. Zina, S. Bundino, and M. G. Pippione, Acrosyringial epidermolytic papulosis neviformis, Dermatologica, vol. 171, no. 2, pp. 122 125, 1985. [3] A. H. Mehregan, Epidermolytic hyperkeratosis. Incidental findings in the epidermis and in the intraepidermal eccrine sweat duct units, Cutaneous Pathology,vol.5,no.2, pp. 76 80, 1978. [4] A.C.S.Hutcheson,P.J.Nietert,andJ.C.Maize, Incidental epidermolytic hyperkeratosis and focal acantholytic dyskeratosis in common acquired melanocytic nevi and atypical melanocytic lesions, the American Academy of Dermatology, vol. 50, no. 3, pp. 388 390, 2004. [5] B. T. Williams and R. J. Barr, Epidermolytic hyperkeratosis in nevi: a possible marker for atypia, American Dermatopathology, vol. 18, no. 2, pp. 156 158, 1996. [6]P.A.ConlinandR.P.Rapini, Epidermolytichyperkeratosis associated with melanocytic nevi: a report of 53 cases, American Dermatopathology, vol. 24, no. 1, pp. 23 25, 2002. [7] C. L. Steele, C. R. Shea, and V. Petronic-Rosic, Epidermolytic hyperkeratosis within infundibular cysts, Cutaneous Pathology, vol. 34, no. 4, pp. 360 362, 2007. [8] A. B. Ackerman, Histopathologic concept of epidermolytic hyperkeratosis, Archives of Dermatology, vol. 102, no. 3, pp. 253 259, 1970. [9] S.J.Lee,Y.Jang,D.Kim,G.Na,andW.Lee, Epidermolytic hyperkeratosis as an incidental finding in drug-induced acne, Dermatology, vol. 32, no. 8, pp. 686 687, 2005. [10] C. L. Steele, C. R. Shea, and V. Petronic-Rosic, Epidermolytic hyperkeratosis within infundibular cysts, Cutaneous Pathology, vol. 34, no. 4, pp. 360 362, 2007. [11] Y. Tokura, M. Takigawa, and M. Yamada, Epidermolytic hyperkeratosis associated with a dilated pore, Dermatology, vol. 14, no. 3, pp. 286 288, 1987. [12] F. Vakilzadeh and R. Happle, Epidermolytic leukoplakia, Cutaneous Pathology, vol. 9, no. 4, pp. 267 270, 1982. [13] L. Requena, C. Schoendorff, and E. Sanchez Yus, Hereditary epidermolytic palmo-plantar keratoderma (Vorner type) report of a family and review of the literature, Clinical and Experimental Dermatology, vol. 16, no. 5, pp. 383 388, 1991. [14] F. G. Aloi and A. Molinero, Nevus comedonicus with epidermolytic hyperkeratosis, Dermatologica, vol. 174, no. 3, pp. 140 143, 1987. [15] S. Barsky, J. A. Doyle, and R. K. Winkelmann, Nevus comedonicus with epidermolytic hyperkeratosis. A report of four cases, Archives of Dermatology, vol. 117, no. 2, pp. 86 88, 1981. [16] D. K. Goette and N. A. Lapins, Epidermolytic hyperkeratosis as an incidental finding in normal oral mucosa. Report of two cases, the American Academy of Dermatology, vol. 10, no. 2, part 1, pp. 246 249, 1984. [17] G. Brodsky, Focal acantholytic dyskeratosis and epidermolytic hyperkeratosis of the oral mucosa adjacent to squamous cell carcinoma, Oral Surgery Oral Medicine and Oral Pathology, vol. 59, no. 4, pp. 388 393, 1985. [18] T. Sasaki and H. Nakajima, Incidental epidermolytic hyperkeratosis in progressive systemic sclerosis, Dermatology, vol. 20, no. 3, pp. 178 179, 1993. [19] C. Urmacher and M. H. Shiu, Malignant melanoma in association with keratosis palmaris et plantaris (epidermolytic hyperkeratosis variant), American Dermatopathology, vol. 7, pp. 187 190, 1985. [20] J. A. Carlson, D. Scott, J. Wharton, and S. Sell, Incidental histopathologic patterns: possible evidence of field cancerization surrounding skin tumors, American Dermatopathology, vol. 23, no. 5, pp. 494 496, 2001. [21] D. J. M. DiMaio and P. R. Cohen, Incidental focal acantholytic dyskeratosis, the American Academy of Dermatology, vol. 38, no. 2 I, pp. 243 247, 1998. [22] R. V. Kolbusz and D. F. Fretzin, Focal acantholytic dyskeratosis in condyloma acuminata, Cutaneous Pathology, vol. 16, no. 1, pp. 44 47, 1989. [23] G. Kolde and F. Vakilzadeh, Leukoplakia of the prepuce with epidermolytic hyperkeratosis: a case report, Acta Dermato- Venereologica, vol. 63, no. 6, pp. 571 573, 1983. [24] P. B. Googe, S. J. Chung, J. Simmons, and R. King, Giantsized condyloma of the breast with focal acantholytic changes, Cutaneous Pathology, vol. 27, no. 6, pp. 319 322, 2000. [25] G. F. Kao and V. I. Sulica, Focal acantholytic dyskeratosis occurring in pityriasis rubra pilaris, American Dermatopathology, vol. 11, no. 2, pp. 172 176, 1989. [26] W. D. Hoover and J. C. Maize, Focal acantholytic dyskeratosis occurring in pityriasis rubra pilaris, American Dermatopathology, vol. 12, no. 3, pp. 321 323, 1990. [27] C. B. Tannenbaum, R. C. Billick, and H. Srolovitz, Multiple cutaneous malignancies in a patient with pityriasis rubra pilaris and focal acantholytic dyskeratosis, the American Academy of Dermatology, vol. 35, no. 5, pp. 781 782, 1996.

Skin Cancer 5 [28] E. L. Garcia Silva, Dysqueratose acantolitica focal em verruca seborreica, Medicina Cutanea Ibero-Latino-Americana, vol.8, no. 4 6, pp. 125 128, 1980. [29] G. Rodsky, Focal acantholyic dyskeratosis and epidermolyic hyperkeratosis of the oral mucosa adjacent to squamous cell carcinoma, Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology, vol. 59, pp. 388 393, 1985. [30] M.L.CintraandE.M.deSouza, Focalacantholyticdyskeratosis: a snare for the pathologist. Report of two cases associated to psoriasis and fibrous papule of the nose, Revista Paulista de Medicina, vol. 110, no. 5, pp. 237 240, 1992. [31] J. K. Stern, J. E. Wolf, and T. Rosen, Focal acantholytic dyskeratosis in pityriasis rosea, Archives of Dermatology, vol. 115, no. 4, article 497, 1979. [32] M. Grossin and S. Belaich, Another case of focal acantholyitc dyskeratosis in the anal canal, American Dermatopathology, vol. 15, no. 2, pp. 194 195, 1993. [33] M. Vazquez Botet and J. L. Sanchez, Vesiculation of focal acantholytic dyskeratosis in acral lentiginous malignant melanoma, Dermatologic Surgery and Oncology,vol. 5, no. 10, pp. 798 800, 1979. [34] Y. E. Sanchez, E. Martin-Dorado, E. Lopez-Negrette et al., Incidental epidermolytic hyperkeratosis (IEH); an epidemiologic study, American Dermatopathology, vol. 22, article 352, 2000. [35] E. Sanchez Yus, L. Requena, P. Simon, and C. Martin de Hijas, Incidental acantholysis, Cutaneous Pathology, vol. 20, no. 5, pp. 418 423, 1993.

MEDIATORS of INFLAMMATION The Scientific World Journal Gastroenterology Research and Practice Diabetes Research International Endocrinology Immunology Research Disease Markers Submit your manuscripts at BioMed Research International PPAR Research Obesity Ophthalmology Evidence-Based Complementary and Alternative Medicine Stem Cells International Oncology Parkinson s Disease Computational and Mathematical Methods in Medicine AIDS Behavioural Neurology Research and Treatment Oxidative Medicine and Cellular Longevity