344 results match your criteria Anetoderma


Optimal Timing of Surgical Excision in Pediatric Pilomatricoma: Association between Clinicopathological Features and Cosmetic Outcomes.

Ann Dermatol 2020 Apr 11;32(2):93-100. Epub 2020 Mar 11.

Department of Dermatology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Korea.

Background: The treatment of choice for pilomatricomas is surgical excision; however, data for the optimal timing of treatment and cosmetic outcomes are limited.

Objective: This study aimed to investigate the optimal timing of treatment in pilomatricomas by considering clinicopathological findings and cosmetic outcomes.

Methods: Seventy-three pilomatricomas patients aged ≤15 years were retrospectively reviewed. Read More

View Article and Full-Text PDF

Secondary Anetoderma.

JAMA Dermatol 2021 Apr 14. Epub 2021 Apr 14.

Department of Dermatology, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.

View Article and Full-Text PDF

Lupus erythematosus: Significance of dermatologic findings.

Ann Dermatol Venereol 2021 Mar 19;148(1):6-15. Epub 2021 Jan 19.

Faculty of medicine, University of Strasbourg, and Dermatology clinic, Strasbourg university hospital, Strasbourg, France. Electronic address:

Herein, the different skin manifestations in patients with lupus erythematosus are reviewed, and their diagnostic, pathogenic and prognostic relevance are discussed, as well as their impact on therapeutic choices. The so-called specific lesions of LE result from an autoimmune pathomechanism and they allow diagnosis of LE by simple clinicopathological correlation since the findings are characteristic. They include the classic acute, subacute and chronic variants, characterised microscopically by interface dermatitis; the dermal variants of lupus, such as tumid lupus, displaying dermal perivascular lymphocytic infiltrate with mucin deposition under the microscope, and lupus profundus, in which lymphocytic lobular panniculitis progressing to hyaline fibrosis is found. Read More

View Article and Full-Text PDF

Anetoderma in a patient with a history of primary syphilis.

Clin Case Rep 2020 Dec 7;8(12):3590-3591. Epub 2020 Sep 7.

Department of Dermatology West Los Angeles - Veterans Affairs Hospital (WLA-VA) Los Angeles CA USA.

Anetoderma is a rare cutaneous disorder presenting with atrophic skin lesions. It can be associated with several autoimmune and infectious diseases. With the current resurgence of syphilis, clinicians must be aware of its association with anetoderma. Read More

View Article and Full-Text PDF
December 2020

Anetoderma observed with reflectance confocal microscopy.

G Ital Dermatol Venereol 2020 Oct 9. Epub 2020 Oct 9.

Dermatology Section, Department of Medical, Surgical and Neurological Science, S. Maria alle Scotte Hospital, University of Siena, Siena, Italy.

View Article and Full-Text PDF
October 2020

Anetoderma secondary to cutaneous mastocytosis: a rare occurrence?

Ital J Dermatol Venerol 2021 Apr 17;156(2):252-254. Epub 2020 Sep 17.

Division of Dermatology and Venereology, Department of Surgery and Translational Medicine, University of Florence, Florence, Italy.

View Article and Full-Text PDF

Iatrogenic Anetoderma of Prematurity: A Series of 5 Clinical Cases and Literature Review.

Acta Dermatovenerol Croat 2020 Aug;28(2):70-74

Aleksandra Matić, MD, PhD, Pediatric clinic Institute for Child and Youth Health Care of Vojvodina, Hajduk Veljkova 10, Novi Sad, Serbia;

Iatrogenic anetoderma of prematurity (IAOP) represents a benign iatrogenic dermatosis characterized by focal, well-demarcated areas of atrophic skin in preterm infants. We present the cases of 5 infants diagnosed with IAOP during a 3-year period in a tertiary-care university hospital. Skin atrophy patches were absent at birth in all presented infants, and there was no family history of anetoderma. Read More

View Article and Full-Text PDF

Multibacillary Leprosy Presenting as Anetoderma in a Young Teenager.

Case Rep Dermatol Med 2020 29;2020:8847310. Epub 2020 Jul 29.

Department of Dermatology & Venereology, National Academy of Medical Sciences, Bir Hospital, Kathmandu, Nepal.

Anetoderma presents as a circumscribed area of slack skin. It can present as either primary or secondary, if associated with other conditions. Leprosy is one of the causes of secondary anetoderma, but it is not commonly reported, especially in multibacillary leprosy. Read More

View Article and Full-Text PDF

Disseminated anetoderma associated with antiphospholipid antibodies.

Clin Rheumatol 2020 12 10;39(12):3887-3888. Epub 2020 Aug 10.

Department of Rheumatology, Hospital Universitario "Dr. Jose Eleuterio Gonzalez", Universidad Autónoma de Nuevo León, Monterrey, Nuevo Leon, Mexico.

View Article and Full-Text PDF
December 2020

Use of dermal fat grafts for treating anetoderma with lipoatrophy following involution of hemangiomas.

Pediatr Dermatol 2020 Jul 22;37(4):776-779. Epub 2020 May 22.

Department of Plastic Surgery, Kobe University Graduate School of Medicine, Kobe, Japan.

Infantile hemangioma (IH) is a benign vascular tumor that gradually involutes over several years. Rapidly involuting congenital hemangioma (RICH) is the relatively rare congenital vascular tumor that is fully grown at birth and does not undergo postnatal growth and involutes during the first year. However, after involution of both IH and RICH, some have severe sequelae, such as redundant skin or conspicuous scarring, requiring additional treatment. Read More

View Article and Full-Text PDF

Primary anetoderma of Jadassohn-Pellizzari: A "saclike" skin.

Indian J Dermatol Venereol Leprol 2020 May 15. Epub 2020 May 15.

Department of Dermatology, Chang Gung Memorial Hospital, Linkou Branch; School of Medicine, College of Medicine, Chang Gung University; Graduate Institute of Clinical Medical Sciences, Chang Gung University, Taoyuan, Taiwan.

View Article and Full-Text PDF

Dermoscopic and Immunohistochemical Observations in Anetodermic Pilomatricoma: A Case Report.

Acta Derm Venereol 2020 Mar 18;100(6):adv00088. Epub 2020 Mar 18.

Department of Dermatology, Affiliated Hospital of Guangdong Medical University, 524001 Zhanjiang, China.

View Article and Full-Text PDF

Anetoderma: an alert for antiphospholipid antibody syndrome.

An Bras Dermatol 2020 Jan - Feb;95(1):123-125. Epub 2019 Dec 18.

Department of Pathology, Universidade do Oeste Paulista, Presidente Prudente, SP, Brazil.

View Article and Full-Text PDF

One case of anetoderma post-vitamin K injection in a newborn.

Int J Dermatol 2020 May 20;59(5):e168-e169. Epub 2020 Jan 20.

Institute of Dermatology, Catholic University and Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Rome, Italy.

View Article and Full-Text PDF

Anetoderma Schweninger-Buzzi: Two Case Reports.

Open Access Maced J Med Sci 2019 Sep 19;7(18):3093-3095. Epub 2019 Aug 19.

Military Medical Academy of Belgrade, Belgrade, Serbia.

Background: Anetodermas are rare disorders of connective tissue with a focal loss of elastic fibres in the upper and mid dermis. Two types are separated, inflammatory and non-inflammatory.

Case Reports: We report two cases of acquired anetoderma Schweniger-Buzzi type. Read More

View Article and Full-Text PDF
September 2019

[Pseudoxanthoma elasticum-like papillary dermal elastolysis: A case report].

Ann Dermatol Venereol 2020 Mar 12;147(3):194-197. Epub 2019 Dec 12.

Service de dermatologie, CHRU Besançon, 3, boulevard Alexandre-Fleming, 25000 Besançon, France.

Background: Pseudoxanthoma elasticum-like papillary dermal elastolysis (PXE-PDE) is a rare disease clinically resembling pseudoxanthoma elasticum (PXE). Herein we report a typical case.

Patients And Methods: A 77-year-old woman consulted for an acquired papular eruption present for 4 years. Read More

View Article and Full-Text PDF

Six cases of perforating pilomatricoma: Anetodermic changes with expression of matrix metalloproteinases.

J Dermatol 2020 Jan 1;47(1):82-85. Epub 2019 Nov 1.

Department of Dermatology, Iwate Medical University School of Medicine, Morioka, Japan.

Perforating pilomatricoma (PP) is a rare clinical variant of pilomatricoma presenting as a crusted or ulcerated nodule. Previous reports have suggested that the tumor cells perforate the epidermis through a process of transepithelial elimination. Here, we report six cases of PP and examine the mechanism of transepithelial elimination in PP. Read More

View Article and Full-Text PDF
January 2020

A Rare Case of Atrophic Dermatofibroma Featuring Linear Skin Dimple.

Case Rep Dermatol 2019 Sep-Dec;11(3):256-259. Epub 2019 Sep 30.

Department of Dermatology, Osaka University Graduate School of Medicine, Suita, Japan.

Dermatofibroma (DF) is a benign skin tumor that is well-known among dermatologists. We herein present a rare case of atrophic dermatofibroma presenting linear skin dimpling. The patient was a 25-year-old woman with a history of wild-type recessive dystrophic epidermolysis bullosa who had noticed linear concavity on her right lateral back 1 year before her initial presentation. Read More

View Article and Full-Text PDF
September 2019

Anetoderma associated with antiphospholipid syndrome.

Med Clin (Barc) 2020 04 28;154(7):288. Epub 2019 Jul 28.

Departamento de Dermatología, Hospital Regional Universitario de Málaga, Málaga, España.

View Article and Full-Text PDF

Lepromatous leprosy masquerading as anetoderma in a boy.

Indian J Dermatol Venereol Leprol 2020 Mar-Apr;86(2):176-177

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

View Article and Full-Text PDF
December 2020

Cutaneous Elastic Tissue Anomalies.

Am J Dermatopathol 2019 Feb;41(2):85-117

Department of Dermatology, Fundación Jiménez Díaz, Universidad Autónoma, Madrid, Spain.

After a review of the physiology in the formation and degradation of cutaneous elastic tissue, we describe the clinicopathologic disorders characterized by increased and decreased cutaneous elastic tissue. Cutaneous disorders characterized by increased and/or abnormal elastic tissue in the dermis include elastoma, also named nevus elasticus, dermatosis lenticularis disseminata, pseudoxanthoma elasticum, late-onset focal dermal elastosis, linear focal elastosis, elastoderma, elastofibroma dorsi, and elastosis perforans serpiginosa. In some of these conditions, the specific histopathologic diagnosis may be rendered with hematoxylin-eosin stain, whereas in other ones special elastic tissue stains are necessary to demonstrate the anomalies. Read More

View Article and Full-Text PDF
February 2019

Hypocellular medallion-like dermal dendrocyte hamartoma on the abdomen of a 25 year old male.

J Cutan Pathol 2019 Apr 10;46(4):297-300. Epub 2019 Feb 10.

Department of Dermatology, Philadelphia College of Osteopathic Medicine, Roswell, Georgia.

Medallion-like dermal dendrocyte hamartoma is a rare congenital lesion that is more commonly seen in females. It often presents at birth on the neck or upper trunk as a well-circumscribed, atrophic patch with wrinkling of the overlying skin. Clinically, the differential diagnosis includes atrophoderma, anetoderma, and congenital atrophic dermatofibrosarcoma protuberans. Read More

View Article and Full-Text PDF

Anetoderma and Systemic Lupus Erythematosus: Case Report and Literature Review.

Acta Derm Venereol 2019 Mar;99(3):335-336

Department of Dermatology, Pontevedra University Hospital, EOXI Pontevedra-Salnés, Centro de Especialidades Mollavao, c/ Simón Bolívar s/n., ES-36001 Pontevedra, Spain.

View Article and Full-Text PDF

Japanese familial anetoderma: A report of two cases and review of the published work.

J Dermatol 2018 Dec 15;45(12):1459-1462. Epub 2018 Oct 15.

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

Anetoderma is a rare cutaneous disorder characterized by focal loss of dermal elastic tissue, resulting in macular atrophy or herniated saclike skin. Some families with hereditary anetoderma have been described, but there have been no reports on Japanese familial anetoderma so far. We herein report two Japanese sibling cases of primary anetoderma. Read More

View Article and Full-Text PDF
December 2018

[Multifocal chalazodermic amyloidosis: The concept of immunoglobulinemic elastopathy].

Ann Dermatol Venereol 2018 Dec 9;145(12):777-784. Epub 2018 Oct 9.

Clinique dermatologique, université de Strasbourg, hôpitaux universitaires de Strasbourg, 1 place de l'hôpital, 67091, Strasbourg, France.

Introduction: Impairment of dermal elastic tissue occurs in different entities associated with immunoglobulins or immunoglobulin-derived protein-secreting clonal plasma cell proliferations, such as amyloid elastosis, anetodermic nodular amyloidosis or monoclonal gammopathy-associated cutis laxa. We report a case of cutaneous immunoglobulinemic amyloidosis revealed by a unique chalazodermic presentation and we review elastic tissue impairment in patients with monoclonal gammopathies.

Observation: A 67-year-old woman consulted for non-infiltrated anetodermic lesions on the upper left quadrant of her abdomen present for ten years. Read More

View Article and Full-Text PDF
December 2018

Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence.

J Dtsch Dermatol Ges 2018 Oct;16(10):1289-1295

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Endocrinology and Diabetology, Saarland University Medical Center, Homburg, Germany.

With an incidence of 1 in 700 births, Down syndrome (DS) is not an uncommon condition. It is associated with various disorders of different organ systems. Serious disorders include cardiac defects and leukemia. Read More

View Article and Full-Text PDF
October 2018