Irritated Nevus and Meyerson's Nevus
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Clinical Features of Benign Tumors of the External Auditory Canal According to Pathology
Central Annals of Otolaryngology and Rhinology Research Article *Corresponding author Jae-Jun Song, Department of Otorhinolaryngology – Head and Neck Surgery, Korea University College of Clinical Features of Benign Medicine, 148 Gurodong-ro, Guro-gu, Seoul, 152-703, South Korea, Tel: 82-2-2626-3191; Fax: 82-2-868-0475; Tumors of the External Auditory Email: Submitted: 31 March 2017 Accepted: 20 April 2017 Canal According to Pathology Published: 21 April 2017 ISSN: 2379-948X Jeong-Rok Kim, HwibinIm, Sung Won Chae, and Jae-Jun Song* Copyright Department of Otorhinolaryngology-Head and Neck Surgery, Korea University College © 2017 Song et al. of Medicine, South Korea OPEN ACCESS Abstract Keywords Background and Objectives: Benign tumors of the external auditory canal (EAC) • External auditory canal are rare among head and neck tumors. The aim of this study was to analyze the clinical • Benign tumor features of patients who underwent surgery for an EAC mass confirmed as a benign • Surgical excision lesion. • Recurrence • Infection Methods: This retrospective study involved 53 patients with external auditory tumors who received surgical treatment at Korea University, Guro Hospital. Medical records and evaluations over a 10-year period were examined for clinical characteristics and pathologic diagnoses. Results: The most common pathologic diagnoses were nevus (40%), osteoma (13%), and cholesteatoma (13%). Among the five pathologic subgroups based on the origin organ of the tumor, the most prevalent pathologic subgroup was the skin lesion (47%), followed by the epithelial lesion (26%), and the bony lesion (13%). No significant differences were found in recurrence rate, recurrence duration, sex, or affected side between pathologic diagnoses. -
CASE REPORT Intradermal Nevus of the External Auditory Canal
Int. Adv. Otol. 2009; 5:(3) 401-403 CASE REPORT Intradermal Nevus of the External Auditory Canal: A Case Report Sedat Ozturkcan, Ali Ekber, Riza Dundar, Filiz Gulustan, Demet Etit, Huseyin Katilmis Department of Otorhinolaryngology and Head and Neck Surgery ‹zmir Atatürk Research and Training Hospital, Ministry of Health, ‹ZM‹R-TURKEY (SO, AE, FG, DE, HK) Department of Otorhinolaryngology and Head and Neck Surgery Etimesgut Military Hospital , ANKARA-TURKEY (RD) Intradermal nevus is the most common skin tumor in humans; however, its occurrence in the external auditory canal (EAC) is uncommon. The clinical manifestations of pigmented nevus of the EAC have been reported to include ear fullness, foreign body sensation, hearing impairment, and otalgia, but some cases were asymptomatic and were found incidentally. The treatment of choice for a symptomatic intradermal nevus in the EAC is complete excision. There has been no recurrence reported in the literature . A pedunculated, papillomatous hair-bearing lesion was detected in the external auditory canal of the patient who was on follow-up for pruritus. Clinical and pathologic features of an intradermal nevus of the external auditory canal are presented, and the literature reviewed. Submitted : 14 October 2008 Revised : 01 July 2009 Accepted : 09 July 2009 Intradermal nevus is the most common skin tumor in left external auditory canal. Otomicroscopic humans; however, its occurrence in the external examination revealed a pedunculated, papillomatous auditory canal (EAC) is uncommon [1-4]. Intradermal hair-bearing lesion in the postero-inferior cartilaginous nevus is considered to be a form of benign cutaneous portion of the external auditory canal (Figure 1). -
Acral Compound Nevus SJ Yun S Korea
University of Pennsylvania, Founded by Ben Franklin in 1740 Disclosures Consultant for Myriad Genetics and for SciBase (might try to sell you a book, as well) Multidimensional Pathway Classification of Melanocytic Tumors WHO 4th Edition, 2018 Epidemiologic, Clinical, Histologic and Genomic Aspects of Melanoma David E. Elder, MB ChB, FRCPA University of Pennsylvania, Philadelphia, PA, USA Napa, May, 2018 3rd Edition, 2006 Malignant Melanoma • A malignant tumor of melanocytes • Not all melanomas are the same – variation in: – Epidemiology – risk factors, populations – Cell/Site of origin – Precursors – Clinical morphology – Microscopic morphology – Simulants – Genomic abnormalities Incidence of Melanoma D.M. Parkin et al. CSD/Site-Related Classification • Bastian’s CSD/Site-Related Classification (Taxonomy) of Melanoma – “The guiding principles for distinguishing taxa are genetic alterations that arise early during progression; clinical or histologic features of the primary tumor; characteristics of the host, such as age of onset, ethnicity, and skin type; and the role of environmental factors such as UV radiation.” Bastian 2015 Epithelium associated Site High UV Low UV Glabrous Mucosa Benign Acquired Spitz nevus nevus Atypical Dysplastic Spitz Borderline nevus tumor High Desmopl. Low-CSD Spitzoid Acral Mucosal Malignant CSD melanoma melanoma melanoma melanoma melanoma 105 Point mutations 103 Structural Rearrangements 2018 WHO Classification of Melanoma • Integrates Epidemiologic, Genomic, Clinical and Histopathologic Features • Assists -
A Case of Intradermal Melanocytic Nevus with Ossification (Nevus of Nanta)
197 A Case of Intradermal Melanocytic Nevus with Ossification (Nevus of Nanta) Young Bok Lee, M.D., Kyung Ho Lee, M.D., Chul Jong Park, M.D. Department of Dermatology, College of Medicine, The Catholic University of Korea, Seoul, Korea A 49-year-old woman presented with a 30-year history of asymptomatic plaque on her right temple. The histological examination revealed nests of nevus cells throughout the entire dermis. Bony spicules were seen just beneath the nevus cell nests in the lower dermis. Cutaneous ossification is an unusual event. Herein, we present a case of intradermal melanocytic nevus with unusual ossification (nevus of Nanta). To the best of our knowledge, this is the first such case report in the Korean literature. (Ann Dermatol (Seoul) 20(4) 197∼199, 2008) Key Words: Melanocytic nevus, Ossification INTRODUCTION drug intake or medical illness. The histological examination showed a dense proliferation of benign Ossification within the skin may occur in a nevus cells in the upper dermis. They were arranged variety of conditions, including pilomatricoma, basal in nests surrounding the hair follicles (Fig. 2). Bony cell carcinoma, appendageal and fibrous prolifera- spicules were seen in the lower dermis, underneath 1,2 tion, inflammation and trauma . The occurrence of the nevus cell nests. Some of them were compact ossification within a melanocytic nevus is an un- while others were surrounded by mature fatty tissue 3-5 usual event . (Fig. 3). Herein, we present a case of intradermal melano- cytic nevus with unusual ossification (nevus of Nanta). To the best our knowledge, this is the first such case report in the Korean literature. -
Two Cases of Nevoid Basal Cell Carcinoma Syndrome in One Family
221 Two Cases of Nevoid Basal Cell Carcinoma Syndrome in One Family Dong Jin Ryu, M.D., Yeon Sook Kwon, M.D., Mi Ryung Roh, M.D., Min-Geol Lee, M.D., Ph.D. Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea The nevoid basal cell carcinoma syndrome, or Gorlin-Goltz syndrome, is an autosomal dominant multiple system disorder with high penetrance and variable expressions, although it can also arise spontaneously. The diagnostic criteria for nevoid basal cell carcinoma syndrome include multiple basal cell carcinomas, palmoplantar pits, multiple odontogenic keratocysts, skeletal anomalies, positive family history, ectopic calcification and neurological anomalies. We report a brother and sister who were both diagnosed with nevoid basal cell carcinoma syndrome. (Ann Dermatol (Seoul) 20(4) 221∼225, 2008) Key Words: Basal cell carcinoma, Nevoid basal cell carcinoma syndrome, Odontogenic keratocyst INTRODUCTION cell carcinoma syndrome. The nevoid basal cell carcinoma syndrome (NBCCS), or Gorlin-Goltz syndrome, is an auto- CASE REPORT somal dominant multiple system disorder with high 1 penetrance and variable expressions . However, Case 1 60% of patients with NBCCS are sporadic cases. It An 11-year-old male was referred to our depart- has an estimated prevalence of 1 in 60,000 with ment for the evaluation of multiple miliary sized 2 equal distributions among males and females . The pigmented macules on the palm and sole that had well-defined diagnostic criteria include cutaneous increased in number over several years. He had an anomalies, dento-facial anomalies, skeletal ano- operation for inguinal hernia at 3 years of age, but malies, positive family history, neurological ano- no other medical problems. -
Acquired Bilateral Nevus of Ota–Like Macules (Hori's Nevus): a Case
Acquired Bilateral Nevus of Ota–like Macules (Hori’s Nevus): A Case Report and Treatment Update Jamie Hale, DO,* David Dorton, DO,** Kaisa van der Kooi, MD*** *Dermatology Resident, 2nd year, Largo Medical Center/NSUCOM, Largo, FL **Dermatologist, Teaching Faculty, Largo Medical Center/NSUCOM, Largo, FL ***Dermatopathologist, Teaching Faculty, Largo Medical Center/NSUCOM, Largo, FL Abstract This is a case of a 71-year-old African American female who presented with bilateral periorbital hyperpigmentation. After failing treatment with a topical retinoid and hydroquinone, a biopsy was performed and was consistent with acquired bilateral nevus of Ota-like macules, or Hori’s nevus. A review of histopathology, etiology, and treatment is discussed below. cream and tretinoin 0.05% gel. At this visit, a Introduction Figure 2 Acquired nevus of Ota-like macules (ABNOM), punch biopsy of her left zygoma was performed. or Hori’s nevus, clinically presents as bilateral, Histopathology reported sparse proliferation blue-gray to gray-brown macules of the zygomatic of irregularly shaped, haphazardly arranged melanocytes extending from the superficial area. It less often presents on the forehead, upper reticular dermis to mid-deep reticular dermis outer eyelids, and nose.1 It is most common in women of Asian descent and has been reported Figure 4 in ages 20 to 70. Classically, the eye and oral mucosa are uninvolved. This condition is commonly misdiagnosed as melasma.1 The etiology of this condition is not fully understood, and therefore no standardized treatment has been Figure 3 established. Case Report A 71-year-old African American female initially presented with a two week history of a pruritic, flaky rash with discoloration of her face. -
Co-Occurrence of Vitiligo and Becker's Nevus: a Case Report
Case Report Olgu Sunumu DOI: 10.4274/turkderm.71354 Turkderm - Arch Turk Dermatol Venerology 2016;50 Co-occurrence of vitiligo and Becker's nevus: A case report Vitiligo ve Becker nevüs birlikteliği: Olgu sunumu Ayşegül Yalçınkaya İyidal, Özge Çokbankir*, Arzu Kılıç** Ağrı State Hospital, Clinic of Dermatology, *Clinic of Pathology, Ağrı, Turkey **Balıkesir University Faculty of Medicine, Department of Dermatology, Balıkesir, Turkey Abstract Vitiligo is an acquired disorder with an unknown etiology in which genetic and non-genetic factors coexist. Melanocytes are destructed in the affected skin areas and clinically depigmented macules and patches appear on the skin. Becker's nevus (BN) appears as hyperpigmented macule, patch or verrucous plaques with sharp and irregular margins and often unilateral occurrence and with associated hypertrichosis in various degrees. Although its pathogenesis is unknown, it is suggested to represent a hamartomatous lesion harboring androgen receptors on the lesion. In this report, we present a 19-year-old male patient who developed vitiligo lesions and then BN adjacent to the vitiligo lesion in the right upper back portion of the body ten years after the initial vitiligo lesion. Keywords: Becker's nevus, vitiligo, co-occurrence Öz Vitiligo nedeni tam olarak bilinmeyen, genetik ve genetik olmayan faktörlerin birlikte rol oynadığı edinsel bir bozukluktur. Bu hastalıkta tutulan deride melanositler ortadan kalkar, klinik olarak depigmente makül ve yamalar belirir. Becker nevüs (BN) sıklıkla unilateral dağılım gösteren, keskin ama düzensiz sınırlı hiperpigmente makül, yama veya verrüköz plakların izlendiği, üzerinde değişik derecelerde hipertrikozun bulunduğu bir hastalıktır. Patogenezi belli olmamakla birlikte hamartamatöz bir lezyon olduğu ve üzerinde androjen reseptörlerinin arttığı ileri sürülmektedir. -
Dermoscopy on Nevus Comedonicus: a Case Report and Review of the Literature
Case report Dermoscopy on nevus comedonicus: a case report and review of the literature Grażyna Kamińska-Winciorek 1, Radosław Śpiewak 2 1The Center for Cancer Prevention and Treatment, Katowice, Poland Head: Beata Wydmańska 2Department of Experimental Dermatology and Cosmetology, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland Head: Prof. Radosław Śpiewak MD. PhD Postep Derm Alergol 2013; XXX, 4: 252 –254 DOI: 10.5114/pdia.2013.37036 Abstract Nevus comedonicus (NC) is a very rare, benign hamartoma characterised by the occurrence of dilated, comedo-like openings, typically on the face, neck, upper arms, chest or abdomen. In uncertain cases, histopathological exami - nation confirms the diagnosis. The authors suggest dermoscopy as a rapid and useful method of initial diagnosis of nevus comedonicus based upon its distinctive dermoscopic features. The dermoscopy reveals numerous light- and dark-brown, circular or barrel-shaped, homogenous areas with prominent keratin plugs. Key words: dermoscopy, dermatoscopy, nevus comedonicus, epidermal nevus, acne vulgaris. Introduction a hypopigmented, slightly hypotrophic, linear spot of Nevus comedonicus (NC) is a benign hamartoma cha - 2 cm × 8 cm (Figure 1). The plugs could not be extracted racterised by the occurrence of dilated comedo-like open - mechanically. The dermoscopic examination revealed ings, with black or brown keratin plugs, typically localised the distinctive pattern consisting of dark, sharply demar - on the face, neck, upper arms, chest or abdomen. The diag - cated keratin plugs of 1–3 mm diameter, numerous struc - nosis of nevus comedonicus is relatively easy. In uncertain tureless, circular- and barrel-shaped, homogenous areas cases, a typical histopathological picture confirms the diag - with hyperkeratotic plugs of various shades of brown nosis. -
The Role of Androgen Receptors in the Clinical Course of Nevus Sebaceus of Jadassohn Katherine S
The Role of Androgen Receptors in the Clinical Course of Nevus Sebaceus of Jadassohn Katherine S. Hamilton, M.D., Sandra Johnson, M.D., Bruce R. Smoller, M.D. Department of Pathology, Vanderbilt University Medical Center, Nashville, Tennessee (KSH); and Departments of Dermatology (SJ, BRS) and Pathology (SJ), University of Arkansas for Medical Services, Little Rock, Arkansas During puberty, they usually enlarge and become Nevus sebaceus of Jadassohn (NSJ) is a benign, con- elevated, verrucous, or nodular and may appear genital hamartoma that often presents at birth, ap- brown (1, 2). In late childhood and adulthood, there pears to regress in childhood, and grows during is a significant risk of developing a secondary tu- puberty, suggesting possible hormonal control. We mor, the most common of which are syringocysta- studied 18 cases of NSJ from children and adults for denoma papilliferum and basal cell carcinoma (1, immunohistochemical evidence of androgen recep- 3). Myriad other cutaneous appendageal neoplasms tor expression. The lesions were evaluated for loca- have also been reported to arise within NSJ. tion and pattern of immunostaining, and these Androgen receptors (AR) are nuclear ligand–de- findings were compared between age groups, sexes, pendent transcription factors of the steroid super- and to androgen receptor expression in normal family that bind testosterone and dihydroxytestos- skin. Androgen receptor positivity was seen in the terone (4). AR have been identified in normal sebaceous glands, in eccrine glands with and with- cutaneous structures and in some epithelial tu- out apocrine change, and rarely in keratinocytes in mors. In normal skin, AR have been localized to the sebaceous nevi. -
Case Report of Giant Congenital Melanocytic Nevus
PEDIATRIC DERMATOLOGY Series Editor: Camila K. Janniger, MD Bathing Trunks Nevus: Case Report of Giant Congenital Melanocytic Nevus Ronald Russ, DO; Lisa Light, MS-IV Bathing trunks nevi, a subtype of giant congeni- 34 years. All maternal and prenatal history was unre- tal melanocytic nevi (CMN), are skin tumors that markable. Upon initial physical examination as a new- present by 2 years of age and occur in a low born (1 hour following delivery), the infant had a large percentage of all births. We report a case of (≥5% body surface area), circumferentially pigmented bathing trunks nevus that was initially suspected area from the umbilicus to mid thigh bilaterally to be melanoma, and describe the history, patho- (Figure 1). Interposed darkened lesions were pres- physiology, and treatment options for CMN. We ent, with 3 distinct, raised, lipomatous-type nodules also discuss the risk for neurocutaneous melano- (2 cm, 1.3 cm, and 3 cm in diameter from left to right) sis (NCM), which is a rare syndrome in patients over the lower lumbar spine (Figure 2). There were no with giant CMN. signs of jaundice, hemolysis, meningomyelocele, or Cutis. 2009;83:69-72. abnormal hair growth. The rest of the physical exami- nation was unremarkable, including cardiovascular, pulmonary, and abdominal systems, and genitourinary athing trunks nevus is a specific subtype of functioning was normal. Cord blood testing revealed giant congenital melanocytic nevus (CMN) A Rh-positive blood type, and a direct Coombs test B with spread resembling bathing trunks. This was negative for antibodies. Complete blood cell rare variant is clinically significant because of the count was within reference range, with the excep- increased risk for progression to melanoma and its tion of a low platelet count of 2343103/µL (reference association with neurocutaneous melanosis (NCM).1 range, 250–4503103/µL). -
Acral Melanoma Toshiaki Saida, Hiroshi Koga, Yoriko Yamazaki, Masaru Tanaka IV.2
Chapter IV.2 Acral Melanoma Toshiaki Saida, Hiroshi Koga, Yoriko Yamazaki, Masaru Tanaka IV.2 Contents thickness, biological behavior is not different among the four histogenetic types [16]. More- IV.2.1 Definition . .196 over, cutaneous melanomas not infrequently IV.2 IV.2.2 Clinical Features . .197 show overlapping histopathological features of IV2.3 Dermoscopic Criteria. 198 the four types [36]. Ackerman repeatedly criti- cized the validity of the Clark’s classification IV.2.4 Relevant Clinical Differential and proposed the unifying concept of melano- Diagnosis. 198 ma [1]. IV.2.5 Histopathology. .199 Recently, Bastian and co-workers defined ac- ral melanoma as melanoma occurring on the IV.2.6 Management. .200 non-hair-bearing skin of the palms or soles or IV.2.7 Case Study. .200 under the nails and found that this type of mel- References. .202 anoma was unique in frequent amplifications of chromosomes 5p15, 5p13, 11q13, and 12q14 [4, 7]. Particularly, amplification of 11q13 was de- tected in ~50% of this type of melanoma. Cyclin D1 is the most important candidate gene located in this chromosome region. It is noteworthy IV.2.1 Definition that 5 of 36 acral melanomas defined by Bastian and co-workers were superficial spreading mel- Acral melanoma is a melanoma that affects ac- anoma according to Clark’s classification [7]. ral areas of the skin, which is the most prevalent Another characteristic of acral melanoma is site of melanoma in non-Caucasians [5, 10]. very low rate of mutation of the BRAF onco- Strictly speaking, acral lentiginous melanoma is gene, which is commonly found in superficial not a synonym for acral melanoma. -
Choroidal Nevus Transformation Into Melanoma: Analysis of 2514 Consecutive Cases
CLINICAL SCIENCES Choroidal Nevus Transformation Into Melanoma Analysis of 2514 Consecutive Cases Carol L. Shields, MD; Minoru Furuta, MD; Edwina L. Berman, BS; Jonathan D. Zahler, MD; Daniel M. Hoberman, BS; Diep H. Dinh, BS; Arman Mashayekhi, MD; Jerry A. Shields, MD Objective: To determine features that are predictive of halo absence (P=.009). A mnemonic device to recall risk growth of choroidal nevi into melanoma. factors of ocular melanoma is “To find small ocular mela- noma using helpful hints,” representing thickness, fluid, Methods: This was a retrospective medical record re- symptoms, orange pigment, margin, ultrasonographic hol- view of 2514 consecutive eyes; Kaplan-Meier estimates lowness, and halo absence. The median hazard ratio for and Cox regression analyses were used. those with 1 to 2 risk factors was 3; for 3 or 4 factors, 5; for 5 to 6 factors, 9; and for all 7 factors, 21. Results: The median tumor basal diameter was 5.0 mm and thickness was 1.5 mm. Nevus growth into mela- Conclusions: In an analysis of 2514 choroidal nevi, fac- noma occurred in 2%, 9%, and 13% of eyes at 1, 5, and tors predictive of growth into melanoma included greater 10 years, respectively. Factors predictive of growth into thickness, subretinal fluid, symptoms, orange pigment, melanoma by multivariable analysis included tumor thick- margin near disc, and 2 new features: ultrasonographic ness greater than 2 mm (PϽ.001), subretinal fluid hollowness and absence of halo. (P =.002), symptoms (P =.002), orange pigment (PϽ.001), tumor margin within 3 mm of the optic disc (P=.001), ultrasonographic hollowness (PϽ.001), and Arch Ophthalmol.