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P2802 Differences in cytokine levels in melanoma patients Jacob Mashiah, MD, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; Jacob Schachter, MD, Ella Institute for Treatment and Research of Melanoma, Sheba Medical Center, Ramat Gan, Israel; Kobi Pessach, MD, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; Sarah Brenner, MD, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel Objective: In view of several studies concerning an observation of an erythematous eruption in the vicinity of or distant from the lesion in melanoma patients, we attempt to assess whether this phenomenon might be related to the blood level of cytokines interleukin (IL)-6 and IL-8. Methods: Sera specimens were obtained from 27 patients with melanoma, of which 15 had erythematous eruptions and 12 did not, and were studied by immunohis- tochemistry for the expression of IL-6 and IL-8. Results: IL-6 was detected in all melanoma patients in both groups. The mean level of IL-6 in the redness group (2.41 pg/L) was significantly higher than in the group without redness (1.25 pg/L). IL-8 was detected in all 27 melanoma patients in the two groups. However, the serum level was \5 pg/L in only one patient (6.7%) in the redness group, and in six patients (50%) in the group without redness, a statistically significant difference. Conclusions: At first glance it appears that the Brenner sign reflects a more advanced disease and heralds a poor prognosis, according to its correlation to the IL-8 and IL-6 blood level. However, in view of the biphasic effect of IL-8 level on tumor progression, and IL-6’s ability to inhibit early stage melanoma, redness in melanoma patients, could serve as a sign of melanoma and has a place in the prognostic factors of the disease. Commercial support: None identified. P2803 Atypical melanosis of the foot, an early lesion of acral lentiginous melanoma in situ: Specific dermatoscopy patterns may precede histo- pathologically recognizable changes Hsiu-Hui Chiu, Department of Dermatology, Chia-Yi Christian Hospital, Chiayi, Taiwan; Shih-Tsung Cheng, MD, Department of Dermatology, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan We present a unique pigmented lesion (2.3 3 2.5 cm) on the third toe of the right foot of a 39-year-old Taiwanese female patient. Clinically, the lesion was character- ized by irregular borders and variegated pigmentation, mimicking acral lentiginous melanoma (ALM). On dermatoscopy, features of melanoma on acral volar skin, such as parallel ridge pattern (PRP), irregular diffuse pigmentation, peripheral dots, and abrupt edge were all noted. However, the histologic findings revealed only melanocytic hyperplasia with minimal cytologic atypia confined to the epidermis. Some melanocytes were present in the lower portion of spinous layer. After reviewing the literature, atypical melanosis of the foot (AMOF) was diagnosed. AMOF was first designated by Nogita et al in 1994. Clinically, these lesions are closely mimicking ALM in situ. However, the histologic findings revealed only focal melanocytic hyperplasia with minimal cytologic atypia along the basal layer. They suggested that the potential for development of malignancy in these cases remained undetermined. We believe that AMOF represented the early phase of acral melanoma in situ by providing the following arguments. First, AMOF fulfill all the clinical criteria for ALM. Second, the dermatoscopic features of AMOF, such as PRP and irregular diffuse pigmentation, are highly specific for ALM. Third, the PRP appeared at a very early development phase of ALM, even chronologically preceding the histopathologically recognizable changes. We suggest that dermatoscopy, which provides a radial overview of the lesion, is a powerful tool for detecting early lesions of acral melanoma in radial growth phase. In certain cases, it could identify early malignant lesion of ALM in situ, not recognizable by vertically-oriented conventional histopathology. Among all of the dermatoscopic features, PRP is most specific and exists at a very early phase. Commercial support: None identified. P2804 Acral lentiginous melanoma: Incidence and survival patterns in the United States, 1986-2004 Porcia Bradford, National Institutes of Health, Rockville, MD, United States; Alisa Goldstein, PhD, National Institutes of Health, Rockville, MD, United States; Margaret Tucker, MD, National Institutes of Health, Rockville, MD, United States; Mary McMaster, MD, National Institutes of Health, Rockville, MD, United States Introduction: Acral lentiginous melanoma (ALM) is the most common type of melanoma found in people of color and is most often found on the palms and soles. Several small single-institution case series of ALM have been published, but have been limited by small sample sizes and have not been population-based. Hence, we conducted a population-based evaluation of ALM to examine its incidence and survival patterns. Methods: Using the Surveillance, Epidemiology, and End Results (SEER) Program of the National Cancer Institute, we evaluated 1683 histologically confirmed cases of ALM reported to 17 cancer registries from 1986 to 2004. Age-adjusted (2000 US standard) incidence and relative survival rates were calculated with SEER*stat software version 6.3.5 and analyzed with PROC FREQ of SAS and PROC LIFETEST of SAS (version 9.1.3). Results: The age-adjusted ALM incidence rate was 1.9 per 1,000,000. The annual percentage change (APC) for ALM was 1.0, unlike CMM, where the incidence has increased over time with an APC of 3.1 (P \.05). The incidence rate for ALM among racial groups was similar, with the exception of Asian/Pacific Islanders who had a statistically lower incidence rate of 1.4 (P ¼.01). The proportion of ALM among all other melanoma subtypes was greatest in people of color, with blacks having the highest percentage of 37%. Overall, ALM had 5- and 10-year relative survival rates of 82.2% and 72.7%, respectively, which were significantly lower than for all CMM, with rates of 88.8% and 86.9% (P \.01). Five- and 10-year survival rates for ALM were highest in non-Hispanic whites (84.9% and 74.1%) and lowest in Asian/Pacific Islanders (70.5% and 56.9%). ALM thickness correlated with survival in different racial groups. ALM was most frequently thin (0.01-1.00 mm) in non-Hispanic whites (45%). The highest percentage of thick ALM ( [4.00 mm) was seen in Asian/Pacific Islanders (25%). Conclusions: ALM is the least frequent of the four major histologic subtypes of CMM overall, but the most frequent subtype among people of color. The incidence of ALM in the United States has remained steady over time, unlike CMM overall, where the incidence has been steadily increasing. ALM is associated with a worse prognosis than CMM overall. Asian/Pacific Islanders have worse survival rates than other groups, and factors such as increased tumor thickness and more advanced stage at presentation are the most likely explanations. Commercial support: None identified. P2805 The use of imiquimod to minimize the surgical defect when excising invasive malignant melanoma surrounded by melanoma in situ, lentigi- nous type Tricia A. Missall, MD, Saint Louis University School of Medicine, St Louis, MO, United States; Scott W. Fosko, MD, Saint Louis University School of Medicine, St Louis, MO, United States Malignant melanoma in situ, lentiginous type or lentigo maligna (LM) is known to have a protracted radial growth phase, which may eventually develop an invasive component or lentigo maligna melanoma (LMM). For this reason, in most patients with LMM, there is surrounding LM. For both LM and LMM, the recommended first- line treatment is surgical excision. Because LM lesions may become large and ill- defined and are often found on the head and neck, this treatment alone may cause significant morbidity and mortality. There is the additional management challenge of discerning the histopathologic extent and hence, the tumor-free margins of these lesions. Based on recent reports of successful treatment of LM with topical imiquimod cream, we have managed selected patients who refused the recom- mended surgical therapy with a combination of treatment modalities to minimize their surgical defect and recovery time, but to ultimately attempt to provide a useful management approach. Two cases of extensive melanoma in situ, lentiginous type with an identified focal area of invasive malignant melanoma were treated with a combination of initial surgical excision for the invasive component followed by topical 5% imiquimod cream for the surrounding in situ disease. After initial surgery and 62 to 65 days of imiquimod therapy, with posttreatment biopsies both patients in this study have no histologic evidence of residual LM, with clinical follow-up of 16 to 20 months. Imiquimod may be a useful adjunctive treatment for extensive LM in combination with surgical excision for an invasive component. Commercial support: None identified. AB132 JAM ACAD DERMATOL MARCH 2009

Differences in cytokine levels in melanoma patients

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Page 1: Differences in cytokine levels in melanoma patients

P2802Differences in cytokine levels in melanoma patients

Jacob Mashiah, MD, Tel Aviv-Sourasky Medical Center, Tel Aviv, Israel; JacobSchachter, MD, Ella Institute for Treatment and Research of Melanoma, ShebaMedical Center, Ramat Gan, Israel; Kobi Pessach, MD, Tel Aviv-Sourasky MedicalCenter, Tel Aviv, Israel; Sarah Brenner, MD, Tel Aviv-Sourasky Medical Center,Tel Aviv, Israel

Objective: In view of several studies concerning an observation of an erythematouseruption in the vicinity of or distant from the lesion in melanoma patients, weattempt to assess whether this phenomenon might be related to the blood level ofcytokines interleukin (IL)-6 and IL-8.

Methods: Sera specimens were obtained from 27 patients with melanoma, of which15 had erythematous eruptions and 12 did not, and were studied by immunohis-tochemistry for the expression of IL-6 and IL-8.

Results: IL-6 was detected in all melanoma patients in both groups. The mean level ofIL-6 in the redness group (2.41 pg/L) was significantly higher than in the groupwithout redness (1.25 pg/L). IL-8 was detected in all 27 melanoma patients in thetwo groups. However, the serum level was\5 pg/L in only one patient (6.7%) in theredness group, and in six patients (50%) in the group without redness, a statisticallysignificant difference.

Conclusions: At first glance it appears that the Brenner sign reflects a more advanceddisease and heralds a poor prognosis, according to its correlation to the IL-8 and IL-6blood level. However, in view of the biphasic effect of IL-8 level on tumorprogression, and IL-6’s ability to inhibit early stage melanoma, redness in melanomapatients, could serve as a sign of melanoma and has a place in the prognostic factorsof the disease.

AB132

cial support: None identified.

Commer

P2803Atypical melanosis of the foot, an early lesion of acral lentiginousmelanoma in situ: Specific dermatoscopy patterns may precede histo-pathologically recognizable changes

Hsiu-Hui Chiu, Department of Dermatology, Chia-Yi Christian Hospital, Chiayi,Taiwan; Shih-Tsung Cheng, MD, Department of Dermatology, Kaohsiung MedicalUniversity Hospital, Kaohsiung, Taiwan

We present a unique pigmented lesion (2.3 3 2.5 cm) on the third toe of the rightfoot of a 39-year-old Taiwanese female patient. Clinically, the lesion was character-ized by irregular borders and variegated pigmentation, mimicking acral lentiginousmelanoma (ALM). On dermatoscopy, features of melanoma on acral volar skin, suchas parallel ridge pattern (PRP), irregular diffuse pigmentation, peripheral dots, andabrupt edge were all noted. However, the histologic findings revealed onlymelanocytic hyperplasia with minimal cytologic atypia confined to the epidermis.Some melanocytes were present in the lower portion of spinous layer. Afterreviewing the literature, atypical melanosis of the foot (AMOF) was diagnosed.AMOF was first designated by Nogita et al in 1994. Clinically, these lesions are closelymimicking ALM in situ. However, the histologic findings revealed only focalmelanocytic hyperplasia with minimal cytologic atypia along the basal layer. Theysuggested that the potential for development of malignancy in these cases remainedundetermined. We believe that AMOF represented the early phase of acralmelanoma in situ by providing the following arguments. First, AMOF fulfill all theclinical criteria for ALM. Second, the dermatoscopic features of AMOF, such as PRPand irregular diffuse pigmentation, are highly specific for ALM. Third, the PRPappeared at a very early development phase of ALM, even chronologically precedingthe histopathologically recognizable changes. We suggest that dermatoscopy, whichprovides a radial overview of the lesion, is a powerful tool for detecting early lesionsof acral melanoma in radial growth phase. In certain cases, it could identify earlymalignant lesion of ALM in situ, not recognizable by vertically-oriented conventionalhistopathology. Among all of the dermatoscopic features, PRP is most specific andexists at a very early phase.

cial support: None identified.

Commer

J AM ACAD DERMATOL

P2804Acral lentiginous melanoma: Incidence and survival patterns in the UnitedStates, 1986-2004

Porcia Bradford, National Institutes of Health, Rockville, MD, United States; AlisaGoldstein, PhD, National Institutes of Health, Rockville, MD, United States;Margaret Tucker, MD, National Institutes of Health, Rockville, MD, United States;Mary McMaster, MD, National Institutes of Health, Rockville, MD, United States

Introduction: Acral lentiginous melanoma (ALM) is the most common type ofmelanoma found in people of color and is most often found on the palms and soles.Several small single-institution case series of ALM have been published, but havebeen limited by small sample sizes and have not been population-based. Hence, weconducted a population-based evaluation of ALM to examine its incidence andsurvival patterns.

Methods: Using the Surveillance, Epidemiology, and End Results (SEER) Program ofthe National Cancer Institute, we evaluated 1683 histologically confirmed cases ofALM reported to 17 cancer registries from 1986 to 2004. Age-adjusted (2000 USstandard) incidence and relative survival rates were calculated with SEER*statsoftware version 6.3.5 and analyzed with PROC FREQ of SAS and PROC LIFETEST ofSAS (version 9.1.3).

Results: The age-adjusted ALM incidence rate was 1.9 per 1,000,000. The annualpercentage change (APC) for ALM was 1.0, unlike CMM, where the incidence hasincreased over time with an APC of 3.1 (P\.05). The incidence rate for ALM amongracial groups was similar, with the exception of Asian/Pacific Islanders who had astatistically lower incidence rate of 1.4 (P ¼ .01). The proportion of ALM among allother melanoma subtypes was greatest in people of color, with blacks having thehighest percentage of 37%. Overall, ALM had 5- and 10-year relative survival rates of82.2% and 72.7%, respectively, which were significantly lower than for all CMM,with rates of 88.8% and 86.9% (P\.01). Five- and 10-year survival rates for ALM werehighest in non-Hispanic whites (84.9% and 74.1%) and lowest in Asian/PacificIslanders (70.5% and 56.9%). ALM thickness correlated with survival in differentracial groups. ALM was most frequently thin (0.01-1.00 mm) in non-Hispanic whites(45%). The highest percentage of thick ALM ([4.00 mm) was seen in Asian/PacificIslanders (25%).

Conclusions: ALM is the least frequent of the four major histologic subtypes of CMMoverall, but the most frequent subtype among people of color. The incidence of ALMin the United States has remained steady over time, unlike CMM overall, where theincidence has been steadily increasing. ALM is associated with a worse prognosisthan CMM overall. Asian/Pacific Islanders have worse survival rates than othergroups, and factors such as increased tumor thickness and more advanced stage atpresentation are the most likely explanations.

cial support: None identified.

Commer

P2805The use of imiquimod to minimize the surgical defect when excisinginvasive malignant melanoma surrounded by melanoma in situ, lentigi-nous type

Tricia A. Missall, MD, Saint Louis University School of Medicine, St Louis, MO,United States; Scott W. Fosko, MD, Saint Louis University School of Medicine,St Louis, MO, United States

Malignant melanoma in situ, lentiginous type or lentigo maligna (LM) is known tohave a protracted radial growth phase, which may eventually develop an invasivecomponent or lentigo maligna melanoma (LMM). For this reason, in most patientswith LMM, there is surrounding LM. For both LM and LMM, the recommended first-line treatment is surgical excision. Because LM lesions may become large and ill-defined and are often found on the head and neck, this treatment alone may causesignificant morbidity and mortality. There is the additional management challenge ofdiscerning the histopathologic extent and hence, the tumor-free margins of theselesions. Based on recent reports of successful treatment of LM with topicalimiquimod cream, we have managed selected patients who refused the recom-mended surgical therapy with a combination of treatment modalities to minimizetheir surgical defect and recovery time, but to ultimately attempt to provide a usefulmanagement approach. Two cases of extensive melanoma in situ, lentiginous typewith an identified focal area of invasive malignant melanoma were treated with acombination of initial surgical excision for the invasive component followed bytopical 5% imiquimod cream for the surrounding in situ disease. After initial surgeryand 62 to 65 days of imiquimod therapy, with posttreatment biopsies both patientsin this study have no histologic evidence of residual LM, with clinical follow-up of16 to 20 months. Imiquimod may be a useful adjunctive treatment for extensive LMin combination with surgical excision for an invasive component.

cial support: None identified.

Commer

MARCH 2009