The ••Spaghetti Technique••: an Alternative to Mohs Surgery Or

Total Page:16

File Type:pdf, Size:1020Kb

The ••Spaghetti Technique••: an Alternative to Mohs Surgery Or The ‘‘spaghetti technique’’: An alternative to Mohs surgery or staged surgery for problematic lentiginous melanoma (lentigo maligna and acral lentiginous melanoma) Caroline Gaudy-Marqueste, MD, PhD,a Anne-Sophie Perchenet, MD,b Anne-Marie Tase´i, MD,c Nika Madjlessi, MD,a Guy Magalon, MD, PhD,b Marie-Aleth Richard, MD, PhD,a and Jean-Jacques Grob, MD, PhDa Marseille, France Background: Lentigo maligna (LM) and acral lentiginous melanoma (ALM) are often large and clinically ill defined. The surgical challenge is to spare tissue while still achieving clear margins. Objective: We sought to provide a retrospective assessment of a two-phase surgical technique for lentiginous melanomas (MM) not suitable for en bloc resection. Methods: In the first phase, a narrow band of skin, ‘‘the spaghetti’’, is resected just beyond the clinical outline of the MM, immediately sutured, and sent for pathological examination without removing the MM. The same procedure is repeated beyond the segments which are shown to be not tumor free and so forth until the minimal tumor-free perimeter is outlined. No operative wound is left between operative sessions. In the second phase, the MM resection and reconstruction are performed at the same time. Results: In 21 patients with LM (n = 16) or ALM (n = 5), the mean operative defect size was 27.5 cm2 (range, 1.97-108.4 cm2). The mean number of steps in the procedure was 1.55 (1-4). Grafts were used for reconstruction in all cases. The relevance of the ‘‘spaghetti’’-defined outline was confirmed in 19 of 21 patients. After a median follow-up period of 25.36 months (range, 0-72 months), the local control rate was 95.24% with one case (4.76%) of in-transit invasive recurrence after 48 months. Limitations: This study was performed at a single center and included a limited number of patients. The follow-up time was relatively brief. Conclusion: The ‘‘spaghetti technique’’ is simple and reliable for LM and ALM. Unlike Mohs surgery, it does not require specific training of surgeons or pathologists. Unlike staged surgery, it does not leave patients with an open wound on the face or soles before final reconstruction. ( J Am Acad Dermatol 2011;64:113-8.) Key words: lentiginous melanomas; margins assessment; surgery. INTRODUCTION Abbreviations used: The lentiginous subtypes of melanoma (MM), ALM: acral lentiginous melanoma LM: lentigo maligna namely lentigo maligna (LM) and acral lentiginous MM: melanoma MM (ALM), share common characteristics: (1) the MMS: Mohs micrographic surgery lentiginous phase can be very subtle with little or no SS: staged surgery From the Service de Dermatologie, Hoˆpital Ste Marguerite,a 4th European Association of Dermato-Oncology Congress, Service de Chirurgie Plastique, Hoˆpital La Conception,b and Marseille, June 19-21, 2008. the Service d’Anatomopathologie, Hoˆpital La Timone, Univer- Reprint requests: Dr Caroline Gaudy-Marqueste, Dermatology site´ de la Me´diterrane´e.c Department, Ste Marguerite Hospital, 270 Blvd Ste Marguerite, Funding sources: None. 13009 Marseille, France. E-mail: [email protected]. Conflict of interest: None declared. 0190-9622/$36.00 This work was presented as an oral communication during the 7th ª 2010 by the American Academy of Dermatology, Inc. International Conference on Adjuvant Therapy of Melanoma e doi:10.1016/j.jaad.2010.03.014 113 114 Gaudy-Marqueste et al JAM ACAD DERMATOL JANUARY 2011 pigmentation and can thus go undetected for months Technique to years before they become nodular or ulcerate and Phase I: Outlining the limits of the MM. After (2) because of clinically ill-defined and not always biopsy confirmation of the LM or ALM diagnosis and pigmented peripheral margins, their extent tends to the obtaining of a provisional Breslow thickness, a 2- be underestimated, with a risk of insufficient resec- mm strip of skin, the so-called ‘‘spaghetti,’’ is tion. Margins of at least 10 mm are therefore usually resected under local anesthesia, 3 to 5 mm beyond recommended for complete excision of LM, even for the clinically apparent perimeter of the tumor (Fig 1). in situ lesions.1-6 LM and ALM The resulting linear defect is grow on skin areas with ma- immediately sutured without jor aesthetic or functional im- CAPSULE SUMMARY ablation of the central area plications (face, soles), including the MM (Fig 1). d Lentiginous melanomas are often large which accounts for the ten- The ‘‘spaghetti’’ is further di- and clinically ill defined. dency to minimize resection, vided into anatomically iden- in a conscious or uncon- d Surgical assessment of margins before tified segments and sent for scious manner, increasing resection is recommended to avoid dermatopathologic examina- the risk of insufficient mar- incomplete resection and to spare tissue. tion. Each segment is ana- gins. Recurrences are there- d The ‘‘spaghetti technique’’ is a simple lyzed along its longitudinal fore frequent, unless a way to evaluate margins and does not axis, in en-face sections. precise control of limits is require special surgical or When a segment of the ‘‘spa- performed, either by the dermatopathology training. ghetti’’ is tumor positive, the techniques of Mohs micro- procedure is repeated 5 mm graphic surgery (MMS) or beyond the corresponding staged surgery (SS). MMS uses frozen horizontal involved segment and again sutured, as shown in sections and gives good results in terms of safety Fig 1, B, so that no operative wound is left between and tissue sparing.2-8 MMS can be performed in 1 day, sessions. The procedure is repeated as often as but is complex and requires specific training; thus it is necessary until the last segment of ‘‘spaghetti’’ is not considered cost-effective in many countries. found to be tumor free. The smallest peripheral area Multi-step variants of MMS with paraffin sections free of any tumor is outlined by the most external line require days or weeks with open wounds. Various SS of sutures of the successive ‘‘spaghetti’’ procedures procedures have been described in the literature.9,10 (see Fig 2) and thus defines the central area to be When SS is applied to large LMs or ALMs, additional resected. Fig 3 represents the first phase of the tissue excisions are often needed until tumor-free procedure showing clinical pictures together with margins can be obtained, allowing for secondary the histologic examination. Fig 4 represents a phase I reconstruction. Patients thus remain with an open procedure photographic sequence. wound on the face or soles with a potential major Phase II. Resection of the tumor and functional, social, and psychological impact. reconstruction. The optimal surgical reconstruc- In the search for a technique more simple than tion to be applied is determined by the final shape of MMS applicable to large LMs and ALMs, combining the area to be resected. Resection of the central area minimal resection with margin control and avoiding and reconstruction (graft or flap) are performed at a prolonged open wound, we designed a two-phase the same time. The final tumor specimen is analyzed procedure based on the sampling of a ‘‘spaghetti- with serial vertical sections. like’’ band of tissue to ascertain margins before Review of the cases. The medical records of all tumor removal. This procedure helps to determine patients treated by this technique between 2002 and the most likely shape and extension of LMs and ALMs 2008 in our Dermatology department were retrospec- before they are resected, so that the patient has a tively reviewed. Clinical, surgical, and histologic data single procedure with immediate reconstruction. were recorded, including demographic data (age and Herein we report our retrospective experience. sex), the tumor location and thickness, the number of steps required in the procedure, the margin status on the final excision report, and the recurrence rate. METHODS Indications RESULTS We used the so-called ‘‘spaghetti technique’’ in Patients patients with ALM or LM who were initially referred Twenty-one patients (4 men and 17 women) for SS. Indications included ill-defined borders, large underwent the ‘‘spaghetti’’ procedure. Mean age at size of lesion, or reconstruction issues. diagnosis was 71 years (range, 53-90 years). JAM ACAD DERMATOL Gaudy-Marqueste et al 115 VOLUME 64, NUMBER 1 Fig 1. A, First step of the procedure. Resection of the ‘‘spaghetti’’ and immediate suture of the defect. B, New ‘‘spaghetti’’ procedure is performed beyond the nonetumor-free segments until tumor-free margins are obtained. C, Second step: Resection of the entire area including the tumor and immediate reconstruction of the defect. Tumor characteristics used grafts in all cases. No immediate complications Twenty one lentiginous MMs were treated, in- occurred. cluding 16 LMs (76.2%) and 5 ALMs (23.8%). All the LMs were located on the face: 8 on the cheek, 3 on the Pathological data ear, one on the temple, one on the eyebrow, one on The mean number of ‘‘spaghetti’’ steps during the nose, one on the inferior eyelid, and one on the phase I was 1.55 (range, 1-4). Several steps were inferior lip. All the ALMs were located on the soles. required in 9 cases. After final excision, 10 MM were Surgical data found to be in situ, whereas 11 were invasive, with a Mean size of the resected area in phase II was mean thickness of 1.90 mm (range, 0.65-10). The 27.54 cm2 (range, 1.97-108.33 cm2). Reconstruction limits of the central skin specimen including the MM 116 Gaudy-Marqueste et al JAM ACAD DERMATOL JANUARY 2011 identified limits of the lentiginous MM, and the objective is to check the periphery of this geometric figure before resection. In the ‘‘spaghetti technique’’, the objective is to define, step by step as closely as possible, the real (pathologically defined) shape and extension of the lentiginous MM, which in turn will allow, a posteriori, determination of the optimal shape and size of the resection for reconstruction.
Recommended publications
  • Critical Evaluation of the So-Called “Junction Nevus”
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector CRITICAL EVALUATION OF THE SO-CALLED "JUNCTION NEVUS* S. WILLIAM BECKER, MS., M.D. The serious study of pigmented nevi was undertaken by many workers in the closing years of the 19th Century. All recognized that the microscopic picture of nevi differed from anything seen in other organs. The presence of nevus cells in both the epidermis and dermis led to concepts of origin at one or the other site, or at both sites. Dermal Origin: Demieville (1) believed that the nevus cells arose from adven- titial and endothelial cells of blood vessels. Bauer (2) and vonRecklinghausen (3) thought that the origin was from endothelium of lymph vessels rather than of blood vessels. Epidermal Origin: According to Abesser (4), Duranti, in 1871, was the first to suggest an epidermal origin of nevus cells. Kromayer (5) stated that the endo- thelium-like cells originate in the basal portion of the epidermis as "Bläschen- zellen", migrate to the dermis and develop connective tissue and elastic fibers, a change which he called "desmoplasia". Abesser (4) agreed that the cells origi- ated in the epithelium and lost their intercellular bridges, but migrated into the dermis as epithelium-like cells, and remained such. Unna (6) advanced the concept that the epithelial cells changed by losing their intercellular bridges and multiplied in groups, a process which he called "Ab- sonderung", then migrated as groups to the dermis, which he called "Abtrop- fung", thus forming pigmented nevi.
    [Show full text]
  • How to Optimize Biopsy Pathology of Melanocytic Lesions
    London, Dermatopathology Study Day 04.12.15 Pigmented lesions of sun-damaged skin W.J. Mooi Department of Pathology, VU university medical center, Amsterdam [email protected] Lentigo maligna Lentigo maligna • Defining combination of features: a substantial proliferation of atypical melanocytes predominantly in lentiginous arrangement, limited to the epithelial compartment of sun-damaged skin, and manifesting as a flat, impalpable hyperpigmentation, usually with irregular contours and with variations of pigmentation. • Spread into hair follicles usually present • Ascent of atypical melanocytes commonly present • Nests are absent or present • The epidermis is commonly flat and thin, but rete ridges may be present • Cellularity, ascent, nesting, degree of atypia vary within the same lesion • Lichenoid inflammatory response sometimes Lentigo maligna: some diagnostic problems • Distinction between paucicellular LM and reactive melanocytic hyperplasia in sun-damaged skin • ‘Grading’ of severity; assessment of risk of invasion: compromised by variations within the same lesion • Interpretation of small numbers of dermal melanocytes in conjunction with LM • Small dermal melanocytic naevi • Scattered isolated dermal ? pre-existent melanocytes • Lichenoid inflammatory response obscuring LM Paucicellular lentigo maligna versus reactive melanocyte hyperplasia in sun-damaged skin LENTIGO MALIGNA REACTIVE MELANOCYTIC HYPERPLASIA Lentiginous spread with or without nests Lentiginous spread only; no nests Melanocytes often directly side-to-side Melanocytes
    [Show full text]
  • Dealing with Lentigo Maligna
    Clinical Dealing with lentigo maligna A challenging case Daniel Mazzoni, Jim Muir more likely with larger lesions and those in higher densities with grouping, on the head and neck.1,2 follicular extension, cytological atypia and even pagetoid spread into the CASE ANSWER 2 upper epidermis. This can make the A man aged 46 years presented to a Ill-defined margins and subclinical determination of clearance of lentigo multidisciplinary team (plastic surgery, extension are common with lentigo maligna difficult.5 radiation oncology, dermatology) with a maligna and, as in this case, lead to A crucial principle is to avoid wound year-long history of a lentigo maligna on involved excision margins.3,4 closures that distort the margin until no the right ear lobe. After initial biopsy, the It can be difficult to differentiate further excisions are needed.3,6 Complex lesion had undergone two wide excisions the histopathological appearance of flaps will distort margins and make with his general practitioner (GP). Both atypical melanocytic hyperplasia seen re-excision problematic. Reconstruction excisions showed margin involvement. in sun-damaged skin from lentigo can be delayed until histopathology The GP referred the patient to a radiation maligna.5 Sun-damaged skin can confirms adequate clearance. oncologist. show features in common with lentigo Confocal microscopy can be used to The initial referral resulted in onward maligna. This includes melanocytes attempt to delineate the extent of lentigo referral to the multidisciplinary team for assessment. Examination revealed a well-healed full thickness skin graft with no clinical or dermoscopic evidence of lentigo maligna (Figure 1).
    [Show full text]
  • Lentigo Maligna Melanoma and Simulants Maui January 2020 Superficial Atypical Melanocytic Proliferations
    Superficial Atypical Melanocytic Proliferations II. Lentigo Maligna Melanoma and Simulants Maui January 2020 Superficial Atypical Melanocytic Proliferations • RGP Melanomas • SSM, LMM, ALM, MLM • Intermediate lesions • Dysplastic nevi, Atypical lentiginous proliferations in high CSD skin; Atypical Acral lentiginous nevi • Superficial atypical melanocytic proliferations • Pagetoid plaque-like Spitz nevi; pigmented spindle cell nevus (Reed) • Special site nevi (genital, breast, scalp, ear, flexural, etc). • Superficial atypical melanocytic proliferations of uncertain significance • Atypical/unusual/uncertain examples of all of the above Superficial Atypical Melanocytic Proliferations • RGP Melanomas • SSM, LMM, ALM, MLM • Intermediate lesions • Dysplastic nevi, Atypical lentiginous proliferations in high CSD skin; Atypical Acral lentiginous nevi • Superficial atypical melanocytic proliferations • Pagetoid plaque-like Spitz nevi; pigmented spindle cell nevus (Reed) • Special site nevi (genital, breast, scalp, ear, flexural, etc). • Superficial atypical melanocytic proliferations of uncertain significance • Atypical/unusual/uncertain examples of all of the above High CSD Melanomas and Simulants. D Elder, Maui, HI Jan 2020 Lentigo maligna melanoma Atypical lentiginous nevi/proliferations High CSD: Lentiginous Nevi and Lentigo Maligna Melanoma and Simulant(s) • Lentiginous Melanoma of Sun-Damaged Skin • LMM in situ • LMM invasive • Distinction from Dysplastic Nevi (Dysplastic Nevus-like Melanoma/Nevoid Lentigo Maligna • Lentiginous Nevi of
    [Show full text]
  • Treatment and Outcomes of Melanoma in Acral Location in Korean Patients
    DOI 10.3349/ymj.2010.51.4.562 Original Article pISSN: 0513-5796, eISSN: 1976-2437 Yonsei Med J 51(4):562-568, 2010 Treatment and Outcomes of Melanoma in Acral Location in Korean Patients Mi Ryung Roh, Jihyun Kim, and Kee Yang Chung Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea. Received: May 26, 2009 Purpose: A retrospective study was conducted to review the treatment and out- Revised: October 19, 2009 comes of mainly melanomas in acral location in a single institution in Korea, and Accepted: November 4, 2009 to evaluate the prognostic significance of anatomic locations of the tumor. Materials Corresponding author: Dr. Kee Yang Chung, and Methods: A retrospective review was completed on 40 patients between Department of Dermatology and Cutaneous 2001 and 2006 to obtain pertinent demographic data, tumor data, treatment charac- Biology Research Institute, Yonsei University teristics, and follow-up data. Results: Forty melanoma patients were identified College of Medicine, 250 Seongsan-ro, and analyzed. Of these, 18 were male and 22 were female patients and the mean Seodaemun-gu, Seoul 120-752, Korea. age at the time of diagnosis was 55.9 years. Of the tumors, 65% were located on Tel: 82-2-2228-2080, Fax: 82-2-393-9157 the hands and feet with acral lentiginous melanoma being the most common E-mail: [email protected] histological subtype. Univariate analysis for the overall melanoma survival revealed ∙The authors have no financial conflicts of that the thickness of the tumor and the clinical stage have prognostic significances.
    [Show full text]
  • Managing Melanoma in Situ Kristen L
    Managing Melanoma In Situ Kristen L. Toren, MD, and Eric C. Parlette, MD† Melanoma is a highly aggressive skin cancer with an increasing incidence. Melanoma in situ is an early, non-invasive form in which the tumor is confined to the epidermis. Treatment of melanoma in situ is challenging due to the frequent subclinical microscopic spread and to the presentation on the head and neck in cosmetically sensitive areas with chronic sun damage. Optimizing tumor eradication is imperative to reduce the potential progression into invasive disease and metastasis, all while maintaining cosmesis. Multiple treatment regimens have been implemented for managing difficult melanoma in situ tu- mors. We provide a thorough review of surgical, and non-surgical, management of mela- noma in situ which can pose therapeutic dilemmas due to size, anatomic location, and subclinical spread. Semin Cutan Med Surg 29:258-263 © 2010 Elsevier Inc. All rights reserved. elanoma is a highly aggressive form of skin cancer with ciated with a greater risk of melanoma, with the exception of Man increasing incidence.1 Melanoma in situ (MIS) is an lentigo maligna. Lentigo maligna, unlike other melanomas, early form of melanoma in which the malignancy is confined has a greater association with nonmelanoma skin cancers.3 to the epidermis. According to the American Cancer Society, an estimated 68,720 new cases of malignant melanoma were Diagnostic Criteria reported in 2009, and 53,120 new cases of melanoma in situ. Lentigo maligna is a subtype of MIS found on sun-exposed Melanoma in situ can have a highly variable presentation, areas and accounts for approximately 80% of all MIS tu- from a well-demarcated, small brown macule on healthy- mors.2 With its increasing incidence and being a precursor to appearing skin to an asymmetric, variably pigmented large invasive melanoma, the treatment of MIS, in particular len- patch on grossly actinically damaged skin (Fig.
    [Show full text]
  • Guidelines for the Management of Cutaneous Melanoma 2010 J.R
    BJD BAD GUIDELINES British Journal of Dermatology Revised U.K. guidelines for the management of cutaneous melanoma 2010 J.R. Marsden, J.A. Newton-Bishop,* L. Burrows, M. Cook,à P.G. Corrie,§ N.H. Cox,– M.E. Gore,** P. Lorigan, R. MacKie,àà P. Nathan,§§ H. Peach,–– B. Powell*** and C. Walker University Hospital Birmingham, Birmingham B29 6JD, U.K. *University of Leeds, Leeds LS9 7TF, U.K. Salisbury District Hospital, Salisbury SP2 8BJ, U.K. àRoyal Surrey County Hospital NHS Trust, Guildford GU2 7XX, U.K. §Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 2QQ, U.K. –Cumberland Infirmary, Carlisle CA2 7HY, U.K. **Royal Marsden Hospital, London SW3 6JJ, U.K. The Christie NHS Foundation Trust, Manchester M20 4BX, U.K. ààUniversity of Glasgow, Glasgow G12 8QQ, U.K. §§Mount Vernon Hospital, London HA6 2RN, U.K. ––St James’s University Hospital, Leeds LS9 7TF, U.K. ***St George’s Hospital, London SW17 0QT, U.K. Correspondence Disclaimer Jerry Marsden. These guidelines reflect the best published data available at the time the report was E-mail: [email protected] prepared. Caution should be exercised in interpreting the data; the results of future Accepted for publication studies may require alteration of the conclusions or recommendations in this report. 24 May 2010 It may be necessary or even desirable to depart from the guidelines in the interests of Key words specific patients and special circumstances. Just as adherence to the guidelines may not evidence, guideline, investigation, melanoma, treatment constitute defence against a claim of negligence, so deviation from them should not necessarily be deemed negligent.
    [Show full text]
  • Nevus Spilus
    PEDIATRIC DERMATOLOGY Series Editor: Camila K. Janniger, MD Nevus Spilus Darshan C. Vaidya, MD; Robert A. Schwartz, MD, MPH; Camila K. Janniger, MD Nevus spilus (NS), also known as speckled frequently arises in childhood as an evenly pig- lentiginous nevus (SLN), is a relatively com- mented, brown to black patch that is indistinguish- mon cutaneous lesion that is characterized by able from a junctional melanocytic nevus. Special multiple pigmented macules or papules within types of lentigo simplex are lentiginosis profusa (or a pigmented patch. It may be congenital or LEOPARD syndrome)3,4 and NS. NS is both a len- acquired; however, its etiology remains unknown. tigo and a melanocytic nevus. NS deserves its own place in the spectrum of classification of important melanocytic nevi; as a Clinical Description lentigo and melanocytic nevus, it has the slight NS is a pigmented patch on which multiple darker potential to develop into melanoma. Accordingly, macules or papules appear at a later stage (Figure). we recommend consideration of punch excisions The term spilus is derived from the Greek word spilos of the speckles alone if excision of the entire NS (spot). Three types of NS exist: small or medium is declined. sized (,20 cm), giant, and zosteriform. The lesions Cutis. 2007;80:465-468. may be congenital or acquired, appearing as subtle tan macules at birth or in early childhood and pro- gressing to the more noticeable pigmented black, evus spilus (NS), also known as speckled brown, or red-brown macules and papules over lentiginous nevus (SLN), is a relatively com- months or years.5 NS may occur anywhere on the N mon cutaneous lesion that is characterized by body but is most commonly identified on the torso multiple pigmented macules or papules within a pig- and extremities.
    [Show full text]
  • NOVEMBER 15, 2006 University of Chicago (Map Attached) Enter
    Wednesday - NOVEMBER 15, 2006 University of Chicago (Map attached) • Plans & Policy Committee Meeting: M - 137 / Lectures: Frank Billings Auditorium P- 117 Enter through Wyler Children’s Hospital (the old Children’s Hospital) at 5841 S. Maryland Ave., Chicago, IL • Patient and slide viewing – (DCAM) Duchossois Center for Advanced Medicine: 5758 S. Maryland Ave., Chicago, IL **Parking spaces in the main parking garage are limited. Valet parking is highly recommended. Please see maps for details.** 8:00 a.m. – 10:00 a.m. Room M-137 Plans & Policy Committee Meeting Enter thru Wyler Children’s Hospital main entrance 5841 S. Maryland 9:00 a.m. – 11:00 a.m. P-117 Registration Frank Billings Auditorium Derm Clinic DCAM 6C will also have attendance Enter thru Wyler Children’s Hospital main entrance check in, badge pick-up at P-117 auditorium 5841 S. Maryland 9:00 a.m. – 10:00 a.m. P-117 Resident Lecture – Dr. Thomas N. Darling (Frank Billings Auditorium) 9:30 a.m. – 11:00 a.m. DCAM 6C Patient Viewing Duchossois Center for Advanced Medicine 5758 S. Maryland Ave. 9:30 a.m. – 11:00 a.m. DCAM 1402 Slide Viewing 5758 S. Maryland Ave. 11:00 a.m. – 11:15 a.m. P-117 CDS Business Meeting (Frank Billings Auditorium) 11:15 a.m. – 12:00 p.m. P-117 Guest Lecture – Dr. Thomas N. Darling (Frank Billings Auditorium) 12:00 a.m. – 12:30 p.m. P-117 Lunch (Frank Billings Auditorium) 12:30 p.m. – 2:00 p.m. P-117 Case discussions (Frank Billings Auditorium) Allan Lorincz Lecture Guest Speaker Thomas N.
    [Show full text]
  • Concurrent Ki-67 and P53 Immunolabeling in Cutaneous
    Concurrent Ki-67 and p53 Immunolabeling in Cutaneous Melanocytic Neoplasms: An Adjunct for Recognition of the Vertical Growth Phase in Malignant Melanomas? Zahid Kaleem, M.D., Anne C. Lind, M.D., Peter A. Humphrey, M.D., Ph.D., Robert H. Sueper, M.D., Paul E. Swanson, M.D., Jon H. Ritter, M.D., Mark R. Wick, M.D. Lauren V. Ackerman Laboratory of Surgical Pathology, Washington University Medical Center (ZK, ACL, PAH, PES, JHR), and SmithKline-Beecham Laboratories (RHS), St. Louis, Missouri; and the Robert E. Fechner Laboratory of Surgical Pathology, University of Virginia Health Sciences Center (MRW), Charlottesville, Virginia malignant melanocytic tumor representing the ver- Ki-67 labeling of paraffin sections has been corre- tical growth phase—nodular melanoma—demon- lated with the number of cells in non-Go phases of strated a statistically significant difference from all the replicative cell cycle, and this immunohisto- other lesions in this study with respect to Ki-67 ,␹2) and p53 reactivity (P < .000001 ,008. ؍ chemical technique has been applied to the evalu- index (P ation of a variety of human neoplasms. Similarly, ␹2). Subsequent concurrent use of a Ki-67 threshold immunolabeling for p53 protein has been used to index of 10% and a p53 index of 5% correctly indi- detect mutations in the corresponding gene, as a cated the presence of vertical growth in 75% of reflection of possible cellular transformation in the NMMs, whereas only 8% of radial growth phase same context. Both of these techniques were ap- melanomas of other types were colabeled at the plied to 253 melanocytic tumors of the skin to assess same levels of reactivity for the two markers (P < their possible utility in the diagnosis and subcatego- .00001, ␹2).
    [Show full text]
  • Lentigines Including Lentigo Simplex, Reticulated Lentigo and Actinic Lentigo V.3 Paolo Carli and Camilla Salvini
    Chapter V.3 Lentigines Including Lentigo Simplex, Reticulated Lentigo and Actinic Lentigo V.3 Paolo Carli and Camilla Salvini Contents V.3.1 Simple Lentigo V.3.1 Simple Lentigo. .290 The definition of lentigo simplex (or lentigo V.3.1.1 Definition . .290 simplex) is a common brown melanocytic le- V.3.1.2 Clinical Features . .290 sion, considered to be the precursor of junction- V.3.1.3 Dermoscopic Criteria. 291 al melanocytic nevi. V.3.1.4 Relevant Clinical Differential Diagnosis. 291 V.3.1.5 Histopathology. .291 V.3.1.6 Management. .292 V.3.1.1 Definition V.3.2 Ink-Spot Lentigo . .292 Lentigines are macular increases in melanin V.3.2.1 Definition . .292 pigmentation of the skin that are persistently V.3.2.2 Clinical Features . .292 present. Histopathologically, they show an in- V.3.2.3 Dermoscopic Criteria. 292 crease in the number of melanocytes at the der- V.3.2.4 Relevant Clinical Differential mo-epidermal junction. Lentigines can be clas- Diagnosis. 292 sified in accordance with aetiological factors V.3.2.5 Histopathology. .293 (Table V.3.1). V.3.2.6 Management. .293 V.3.3 Actinic Lentigo. .293 V.3.3.1 Definition . .293 V.3.1.2 Clinical Features V.3.3.2 Clinical Features . .293 Macular area of light-brown or brown-black V.3.3.3 Dermoscopic Criteria. 293 pigmentation, fairly uniform, usually circu- V.3.3.4 Relevant Clinical Differential lar or oval, with 3–5 mm in diameter, although Diagnosis. 293 several individual lentigines may coalesce V.3.3.5 Histopathology.
    [Show full text]
  • Lentigo Maligna
    LENTIGO MALIGNA http://www.aocd.org Lentigo maligna is the precursor to a subtype of melanoma called lentigo maligna melanoma, which is a cancerous (malignant) growth of the cells that give our skin cells color. This variety of melanoma starts as a flat, irregularly bordered brown to tan patch on the skin, typically with variegation in color such that it may darken unevenly over the years. Because of this, the gradual darkening may go unnoticed. The cancer cells may divide and spread locally. If these cancer cells start to spread deeply into the lower layers of the skin (dermis or subcuticular fat), a bump or nodular area may be noticed in the original flat lesion. Once the cells have spread deeply, the term lentigo maligna melanoma is used. When solely the top layer of the skin is affected (epidermis), only the term lentigo maligna is employed. Lentigo maligna is more prevalent in the elderly population who has seen a high level of cumulative sun exposure in their lifetime. Therefore, commonly affected body regions include the face and forearms. Diagnosis may at times be challenging as this lesion could be confused with benign skin findings such as moles, solar lentigines or seborrheic keratoses. Your dermatologist is specially trained to spot subtle differences between these different lesions. He or she may elect to biopsy those skin findings that are suspect. The usual treatment for a lentigo maligna is local excision with a 5mm margin of normal tissue. A larger margin or Mohs surgery may be performed if the edges are unclear. Sometimes a lesion is located in a difficult area to excise.
    [Show full text]