De novo intraepidermal epithelioid melanocytic dysplasia: a review of 263 cases.

Abstract:

BACKGROUND:De novo intraepidermal epithelioid melanocytic dysplasia (DNIEMD) is a newly characterized lesion that is associated with a personal and/or family history of malignant melanoma (MM) and/or dysplastic nevi (DN). However, the biological significance is still uncertain and the persons predisposed to this lesion have not been adequately described. METHODS:Clinicopathologic data of 258 patients, from 263 biopsies diagnosed with DNIEMD, was obtained. A brief voluntary questionnaire was used to obtain demographic, risk factor and disease history. RESULTS:There is an 82% (n=263) predominance of women with DNIEMDs. For men and women, the distributions of these lesions occur on the lower extremities (71%), the upper extremities (24%) and trunk (5%). Thirty-one percent of the 258 patients responded to the questionnaires. 48% of the 60 respondents had green or blue eyes. 26% of 62 respondents had a history of non-melanoma skin cancer (NMSC). Combined data revealed that 68% of 134 patients had a history of DN. As well, 24% of 89 patients had personal histories of melanoma, while 24% of 72 patients had a family history of melanoma. CONCLUSION:Most of these DNIEMD lesions are found on the lower extremities of women and men, and they have an increased association with MM, DN and NMSC.

journal_name

J Cutan Pathol

authors

Jessup CJ,Cohen LM

doi

10.1111/j.1600-0560.2009.01429.x

subject

Has Abstract

pub_date

2010-08-01 00:00:00

pages

852-9

issue

8

eissn

0303-6987

issn

1600-0560

pii

CUP1429

journal_volume

37

pub_type

杂志文章
  • Mucinous hidradenoma: a report of three cases.

    abstract::Mucinous cutaneous adnexal tumors are an uncommon occurrence. We describe three cases of mucinous hidradenoma characterized by diffuse and prominent mucinous cell proliferation and discuss the relevant literature. The patients (two men and one woman) ranged in age from 32 to 72 years. The lesions were completely excis...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2006.00645.x

    authors: Goh SG,Carr R,Dayrit JF,Calonje E

    更新日期:2007-06-01 00:00:00

  • Ultrastructural localization of gap junction protein connexin 43 in normal human skin, basal cell carcinoma, and squamous cell carcinoma.

    abstract::The expression and localization of connexin 43 (Cx43) were investigated in normal human epidermis, pilosebaceous apparatus, basal cell carcinoma, and squamous cell carcinoma by immunofluorescence as well as by immunoelectron microscopy. In the normal epidermis the immunofluorescence was weak in the basal layer, increa...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1997.tb01094.x

    authors: Tada J,Hashimoto K

    更新日期:1997-11-01 00:00:00

  • Elastophagocytosis in extragenital lichen sclerosus.

    abstract:BACKGROUND:Elastophagocytosis, or elastic fiber phagocytosis by multinucleate macrophages, has been observed in different skin conditions that may or may not occur on sun-exposed skin. Although loss of elastic fibers has been well documented in the homogenized papillary dermal zone in lichen sclerosus (LS), elastophago...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2010.01575.x

    authors: Abbas O,Chatrath V,Goldberg LJ

    更新日期:2010-10-01 00:00:00

  • A rare cutaneous adnexal neoplasm: cystic panfolliculoma.

    abstract::A cystic panfolliculoma is a benign follicular neoplasm which recapitulates several portions of the hair follicle. The patient was a 64-year-old Caucasian female who presented with a new growth on her right forearm. The lesion had slowly enlarged over the previous 11 months. She complained of it bleeding on several oc...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.12807

    authors: Neill B,Bingham C,Braudis K,Zurowski S

    更新日期:2016-12-01 00:00:00

  • White sponge nevus presenting as genital lesions in a 28-year-old female.

    abstract::A case is presented of white plaques occurring predominantly on the vulvar mucosa of a 28-year-old female diagnosed as white sponge nevus (WSN). WSN is a rare, autosomal dominant disorder involving mucous membranes. It predominantly affects the oral mucosa; however, it has been reported to rarely involve extraoral muc...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01294.x

    authors: Cutlan JE,Saunders N,Olsen SH,Fullen DR

    更新日期:2010-03-01 00:00:00

  • Cutaneous extranodal NK/T-cell lymphoma mimicking cellulitis an HIV positive patient without lymphopenia.

    abstract::We present the case of a 28-year-old male with a history of human immunodeficiency virus (HIV) with a 1-month history of a steadily enlarging, firm painful lesion on the right posterior shoulder. The patient was initially treated for cellulitis given his clinical picture. Histopathologic examination revealed an angioc...

    journal_title:Journal of cutaneous pathology

    pub_type:

    doi:10.1111/cup.12885

    authors: Malviya N,Rainwater YB,Vandergriff T,Mauskar MM

    更新日期:2017-03-01 00:00:00

  • Clinically unapparent melanocytic nevi on the prepuce.

    abstract:BACKGROUND:Melanocytic nevi from the genitalia are uncommon. Nevi on the vulva are much better described than nevi on male genitalia. To our knowledge, a systematic study of preputial melanocytic nevi has not been reported. OBJECTIVE:To investigate the frequency of clinically unapparent melanocytic nevi on a series of...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2008.01070.x

    authors: Val-Bernal JF,Val D,Garijo MF

    更新日期:2009-04-01 00:00:00

  • Expression of BMI-1 in normal skin and inflammatory and neoplastic skin lesions.

    abstract:BACKGROUND:BMI-1 is involved in the maintenance of stem cells and functions as an oncogene in both lymphomas and solid carcinomas, acting by downregulation of p16ink4a. We have investigated the expression profile of BMI-1 in normal and inflamed skin as well as in basal cell carcinomas (BCCs) and squamous cell carcinoma...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2006.00587.x

    authors: Reinisch CM,Uthman A,Erovic BM,Pammer J

    更新日期:2007-02-01 00:00:00

  • Pigmented neuroectodermal tumor of infancy. A light microscopic and immunohistochemical study.

    abstract::We studied two cases of pigmented neuroectodermal tumor of infancy (PNTI) by routine light microscopy and immunohistochemistry on formalin fixed, paraffin embedded tissues using antibodies to HMB-45 "melanoma associated" antigen, S-100 protein, neuron specific enolase (NSE), Leu-7 antigen, chromogranin, epithelial mem...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1991.tb00600.x

    authors: Argenyi ZB,Schelper RL,Balogh K

    更新日期:1991-02-01 00:00:00

  • Acral keratosis with eosinophilic dermal deposits: a distinctive clinicopatholgic entity or colloid milium redux?

    abstract:AIMS:The differential diagnosis of acral keratoses is broad. Encompassing a variety of infectious, heritable and degenerative disorders, emphasis upon the clinical setting and histologic subtlety are often required to arrive at the correct diagnosis. Herein, we report on a series of adult patients who presented with ag...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2006.00530.x

    authors: Saeed S,Sagatys E,Morgan MB

    更新日期:2006-10-01 00:00:00

  • Androgen receptor overexpression in Becker nevus: histopathologic and immunohistochemical analysis.

    abstract:BACKGROUND:Becker nevus (BN) is a unilateral, hairy, pigmented cutaneous hamartoma that frequently appears in adolescence. Several features of BN suggest that increased androgen sensitivity plays a role in its pathogenesis. There have been only a few studies of histopathologic and immunohistochemical characteristics of...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2008.00988.x

    authors: Kim YJ,Han JH,Kang HY,Lee ES,Kim YC

    更新日期:2008-12-01 00:00:00

  • Grading of atypia in genital skin lesions: routine microscopic evaluation and use of p16 immunostaining.

    abstract:BACKGROUND:p16 immunostaining has been used to aid and improve the histopathologic evaluation of equivocal cervical lesions with associated low-grade or high-grade dysplasia. However, the utility of p16 immunostaining in the diagnosis of atypical genital skin lesions remains debatable. METHODS:We conducted a cross-sec...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12525

    authors: Ezaldein H,Lott JP,McNiff JM,Hui P,Buza N,Ko CJ

    更新日期:2015-08-01 00:00:00

  • Juvenile elastoma (Weidman). An ultrastructural study.

    abstract::Two cases of juvenile elastoma (nevus elasticus in disseminated tumors) were histologically and ultrastructurally investigated. The predominant components of this disseminated dysembryoplasia are abnormal elastic fibers. Both cases showed numerous large elastic fibers with an abundant background matrix. The elastic mi...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1981.tb01001.x

    authors: Ledoux-Corbusier M,Achten G,De Dobbeleer G

    更新日期:1981-06-01 00:00:00

  • Pigmented follicular cysts.

    abstract::This report deals with seven examples of an epithelial cyst for which we have found no proper designation in the classification of epithelial skin cysts. Clinically, the lesion is often hyperpigmented, located in mid-dermis and shows epidermoid keratinization. The cyst contains laminated keratin, many pigmented hair s...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1982.tb01081.x

    authors: Mehregan AH,Medenica M

    更新日期:1982-12-01 00:00:00

  • Antibody to S100a6 protein is a sensitive immunohistochemical marker for neurothekeoma.

    abstract:BACKGROUND:Neurothekeoma is a benign tumor of putative peripheral nerve sheath origin. It occurs in a myxoid (classic) variant, cellular variant, and intermediate (mixed) variant. Cellular neurothekeoma (CNT) usually involves the head and neck or extremities of young patients. Histologically, CNT can be confused with m...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2002.00032.x

    authors: Fullen DR,Lowe L,Su LD

    更新日期:2003-02-01 00:00:00

  • A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12 approximately 12.3 in a Chinese family.

    abstract:BACKGROUND:Hereditary hypotrichosis simplex (MIM 146520, HHS) is a rare form of nonsyndromic alopecia. The locus for autosomal dominant HHS was mapped to 18p11.32-p11.23 and 6p21.3, respectively, suggestive of genetic heterogeneity. AIM:To identify the disease-causing gene for a four-generation Chinese family with dom...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01415.x

    authors: Xu C,Zhang L,Chen N,Su B,Pan CM,Li JY,Zhang GW,Liu Z,Sheng Y,Song HD

    更新日期:2010-07-01 00:00:00

  • Giant and "granular melanosomes" in Leopard syndrome: an ultrastructural study.

    abstract::Electron microscopy of lentigines was performed to study the pigmentation abnormality in two children with LEOPARD syndrome. Giant melanosomes similar to those seen in café-au-lait spots of neurofibromatosis and nevus spilus were found in a lentigine from one of our cases. Our results show that "spherical granular mel...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1976.tb00865.x

    authors: Bhawan J,Purtilo DT,Riordan JA,Saxena VK,Edelstein L

    更新日期:1976-01-01 00:00:00

  • Spindle cell angiosarcoma following irradiation therapy for cervical carcinoma.

    abstract:BACKGROUND:Angiosarcomas arise in the scalp and face in the elderly, in association with chronic lymphedema (Stewart-Treves syndrome), and in irradiated areas. Rarely in these settings, angiosarcomas exhibit pure spindle cell phenotype. METHODS:Herein, the clinicopathologic features of a 72-year-old-woman with spindle...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1034/j.1600-0560.2002.290206.x

    authors: Kiyohara T,Kumakiri M,Kobayashl H,Itoh K,Lao LM,Ohkawara A,Nakmura H

    更新日期:2002-02-01 00:00:00

  • Glomus-like bodies within a neurofibroma: a novel neoplasm arising in neurofibromatosis type 1 or a coincidence?

    abstract::Neurofibromatosis type 1 is a relatively common genetic disorder with variable phenotypes. Tumors with features of both glomus tumors and neurofibromas are exceedingly rare in literature. Herein, we report a not yet described neoplasm with features of both a glomangioma/glomus tumor and a neurofibroma arising in a pat...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12439

    authors: Thareja S,Honigbaum A,Jukic D

    更新日期:2015-04-01 00:00:00

  • Elastic fiber pattern in scleroderma/morphea.

    abstract:BACKGROUND:Scleroderma/morphea is characterized by expansion of the dermis with thickened collagen bundles and loss of CD34(+) dermal dendrocytes. Variable elastic fiber changes have been described, but to our knowledge, no systematic study of the elastic fiber pattern correlated with CD34 expression has been reported....

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01201.x

    authors: Walters R,Pulitzer M,Kamino H

    更新日期:2009-09-01 00:00:00

  • Broad range of adverse cutaneous eruptions in patients on TNF-alpha antagonists.

    abstract::Biologic therapies targeting tumor necrosis factor (TNF)-alpha have become a mainstay in the management of a number of autoimmune diseases. We report a series of adverse skin eruptions in six patients (four females, two males, age: 21-58 years, mean: 39) receiving 4 months to 10 years (mean 3.1 years) of anti-TNF-alph...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2012.01894.x

    authors: Hawryluk EB,Linskey KR,Duncan LM,Nazarian RM

    更新日期:2012-05-01 00:00:00

  • Early histopathology of the cutaneous capillary fragility test (Rumpel-Leede).

    abstract::The characteristic histologic change seen at 2 h in the Rumpel-Leede (Hess) test is, in addition to focal hemorrhage in the upper dermis, a perivascular lymphocyte infiltrate with focal areas of lymphocytic epidermal invasion. The histologic findings, even with the liquefaction degeneration, are similar to those of pu...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1979.tb00300.x

    authors: Duncan SC,Winkelmann RK

    更新日期:1979-02-01 00:00:00

  • Churg-Strauss syndrome with coexistence of eosinophilic vasculitis, granulomatous phlebitis and granulomatous dermatitis in bullous pemphigoid-like blisters.

    abstract::The main histopathological features in the cutaneous lesions of Churg-Strauss syndrome (CSS) are dermal leukocytoclastic vasculitis with a variable eosinophilic infiltrate and non-vasculitic tissue eosinophilia with granuloma formation. This wide histopathological spectrum may account for the various skin manifestatio...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2010.01513.x

    authors: Ishibashi M,Kudo S,Yamamoto K,Shimai N,Chen KR

    更新日期:2011-03-01 00:00:00

  • Sjögren-Larsson syndrome: a dermato-histopathological study.

    abstract::Thirty-six Swedish patients with the recessively inherited Sjögren-Larsson syndrome (SLS) were examined by histopathologic and, in some cases, morphometric techniques. Skin biopsy specimens were taken on the volar side of the right forearm below the cubital fossa. The histopathological picture was characterized by a m...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1982.tb01075.x

    authors: Hofer PA,Jagell S

    更新日期:1982-12-01 00:00:00

  • Unusual expression of S-100 protein in histiocytic neoplasms.

    abstract::Twenty-nine cases of histiocytic neoplasms, some resembling juvenile xanthogranuloma (JXG) and others resembling reticulohistiocytoma (RH), were evaluated. Immunohistochemical stains were performed. In this series, seven cases were identified that expressed S-100 protein positive cells. The S-100 positive cells were p...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1600-0560.1998.tb01704.x

    authors: Tomaszewski MM,Lupton GP

    更新日期:1998-03-01 00:00:00

  • Expression of WT-1 by the vascular component of acral pseudolymphomatous angiokeratoma of children.

    abstract::Acral pseudolymphomatous angiokeratoma of children (APACHE) is a disease comprised by a dense dermal infiltrate of B-lymphocytes and T-lymphocytes in which prominent blood vessels with plump endothelium are found. In the past, the lesion was interpreted as a variant of angiokeratoma, a vascular malformation, or a nevu...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12429

    authors: Fernandez-Flores A,Fierro S,Larralde M

    更新日期:2015-01-01 00:00:00

  • Syndecan-1 expression is diminished in acantholytic cutaneous squamous cell carcinoma.

    abstract::Syndecan-1 is a cell surface proteoglycan predominantly expressed on the surface of adult epithelial cells, and is normally present in all epidermal layers except for the most superficial terminally differentiated cells. Syndecan-1 mediates cell-cell and cell-extracellular matrix adhesion, thereby influencing cell mor...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.1999.tb01862.x

    authors: Bayer-Garner IB,Sanderson RD,Smoller BR

    更新日期:1999-09-01 00:00:00

  • Ulcerated dermatofibroma with osteoclast-like giant cells.

    abstract:BACKGROUND:Ulceration and osteoclast-like giant cells are two pathological features uncommonly seen in dermatofibromas. To our knowledge, the presence of these features has not been previously described within the same lesion. METHODS:We report the clinical, histopathological and immunohistochemical findings of a 38-y...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/j.1600-0560.2009.01195.x

    authors: González-Vilas D,García-Gavín J,Ginarte M,Rodríguez-Blanco I,Toribio J

    更新日期:2009-10-01 00:00:00

  • Follicular mycosis fungoides: a case report and review of the literature.

    abstract:BACKGROUND:Follicular mycosis fungoides is an unusual variant of mycosis fungoides (MF). Unlike classic MF where atypical lymphocytes show a predilection for the epidermis (epidermotropism), follicular MF displays a malignant lymphocytic infiltrate tropic for hair follicles (folliculotropism). This malignant lymphocyti...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章,评审

    doi:10.1034/j.1600-0560.2001.028006318.x

    authors: DeBloom J 2nd,Severson J,Gaspari A,Scott G

    更新日期:2001-07-01 00:00:00

  • Pigmented basal cell carcinoma: increased melanin or increased melanocytes?

    abstract:BACKGROUND:Studies on the precise cause of increased melanization in pigmented basal cell carcinomas (BCC) are limited. We aimed to determine whether the cause of melanization is from increased number of melanocytes or increased melanin pigment, and if there is a difference in the number of melanocytes on different sun...

    journal_title:Journal of cutaneous pathology

    pub_type: 杂志文章

    doi:10.1111/cup.12819

    authors: Brankov N,Prodanovic EM,Hurley MY

    更新日期:2016-12-01 00:00:00