454 results match your criteria Erythema Elevatum Diutinum


Erythema elevatum diutinum: an unusual cutaneous vasculitis associated with rheumatoid arthritis.

Rheumatology (Oxford) 2020 Apr 15. Epub 2020 Apr 15.

Department of Dermatology, Peking University First Hospital, Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, National Clinical Research Center for Skin and Immune Disease, Beijing, China.

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http://dx.doi.org/10.1093/rheumatology/keaa177DOI Listing

Exuberant case of erythema elevatum diutinum in a patient infected with HIV and hepatitis B virus.

An Bras Dermatol 2020 Mar - Apr;95(2):200-202. Epub 2020 Feb 12.

Department of General Medicine, Teaching Hospital, Universidade Federal de Pelotas, Pelotas, RS, Brazil.

Erythema elevatum diutinum is a small vessel vasculitis which is benign, rare, and chronic. It is clinically characterized by violaceous, brown, or yellowish plaques, nodules, and papules. It has been associated with autoimmune, infectious, and neoplastic processes. Read More

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http://dx.doi.org/10.1016/j.abd.2019.02.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175035PMC

Erythema elevatum diutinum of the hand: a peculiar case, successfully treated with tetracyclines.

G Ital Dermatol Venereol 2020 Mar 4. Epub 2020 Mar 4.

Section of Dermatology, Department of Medical Sciences, University of Turin, Turin, Italy.

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http://dx.doi.org/10.23736/S0392-0488.20.06536-0DOI Listing

Erythema Elevatum Diutinum - Two Case Reports, Two Different Clinical Presentations, and a Short Literature Review.

Open Access Maced J Med Sci 2019 Sep 30;7(18):3039-3042. Epub 2019 Aug 30.

Department of Dermatology, University of Rome "G. Marconi", Rome, Italy.

Background: Erythema elevatum diutinum (EED) belongs to the spectrum of cutaneous leukocytoclastic vasculitides. EED is a very rare dermatosis presenting with reddish to browning papules and plaques. EED may be associated with infections, hematologic and autoimmune disorders. Read More

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http://dx.doi.org/10.3889/oamjms.2019.765DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910801PMC
September 2019

Concurrence of erythema elevatum diutinum and HIV infection: A case report and literature review.

JAAD Case Rep 2019 Dec 26;5(12):1093-1096. Epub 2019 Nov 26.

University of Utah School of Medicine, Salt Lake City, Utah.

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http://dx.doi.org/10.1016/j.jdcr.2019.10.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889235PMC
December 2019

Unusual presentation of erythema elevatum diutinum in an HIV-positive man with dramatic response to dapsone.

Int J STD AIDS 2019 11 15;30(13):1337-1339. Epub 2019 Nov 15.

Department of Dermatology and Venereology, All India Institute of Medical Sciences, New Delhi, India.

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http://dx.doi.org/10.1177/0956462419874985DOI Listing
November 2019
1.037 Impact Factor

Hyperpigmented nodule overlying the right Achilles tendon.

JAAD Case Rep 2019 Nov 28;5(11):985-987. Epub 2019 Oct 28.

Department of Dermatology University Hospitals Cleveland Medical Center, Cleveland, Ohio.

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http://dx.doi.org/10.1016/j.jdcr.2019.08.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834969PMC
November 2019

Neutrophil Extracellular Traps are Present in Immune-complex-mediated Cutaneous Small Vessel Vasculitis and Correlate with the Production of Reactive Oxygen Species and the Severity of Vessel Damage.

Acta Derm Venereol 2019 10 30. Epub 2019 Oct 30.

Department of Dermatology, American University of Beirut, PO Box 11-0236, Riad El Solh, Beirut, Lebanon.

Formation of neutrophil extracellular traps has been implicated in autoimmunity. However, the presence and clinical relevance of neutrophil extracellular traps in immune-complex-mediated cutaneous small and medium vessel vasculitides has not been investigated. This study retrospectively analysed 72 patients with histology-proven hypersensitivity vasculitis (n = 21), IgA vasculitis (n = 22), urticarial vasculitis (n = 22), erythema elevatum diutinum (n = 3) and polyarteritis nodosa (n = 4). Read More

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http://dx.doi.org/10.2340/00015555-3363DOI Listing
October 2019

Quetiapine-induced leukocytoclastic vasculitis.

Indian J Pharmacol 2019 Jul-Aug;51(4):282-283

Department of Psychiatry, JSS Medical College, JSS AHER, Mysuru, Karnataka, India.

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http://dx.doi.org/10.4103/ijp.IJP_680_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759529PMC
March 2020
1 Read
0.679 Impact Factor

The late stage of erythema elevatum diutinum mimicking cutaneous spindle-cell neoplasms: a case report and review of the literature.

J Cutan Pathol 2019 Aug;46(8):551-554

Skin Research Center, Shahid Beheshti University of Medical Sciences, Shohada-e Tajrish Hospital, Tehran, Iran.

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http://dx.doi.org/10.1111/cup.13448DOI Listing
August 2019
2 Reads

A rash in a hairy situation: Leukocytoclastic vasculitis at presentation of hairy cell Leukemia.

Am J Hematol 2019 12 23;94(12):1433-1434. Epub 2019 Aug 23.

Division of Hematology and Oncology, Department of Internal Medicine, Loma Linda University, Loma Linda, California.

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http://dx.doi.org/10.1002/ajh.25597DOI Listing
December 2019
3 Reads

A rare case of clomiphene-induced leukocytoclastic vasculitis.

J Basic Clin Physiol Pharmacol 2019 Jul 18;30(4). Epub 2019 Jul 18.

Vardhman Mahavir Medical College and Safdarjung Hospital, Department of Pharmacology, New Delhi, India.

Clomiphene citrate is a first-line drug for the induction of ovulation in infertility cases. Leukocytoclastic vasculitis (LCV) is an extremely rare serious adverse drug reaction to clomiphene. We report here the case of a 30-year-old Indian female patient who presented with generalized petechiae and palpable purpura without fever and sparing the mucosa, temporally related to clomiphene intake and consistent with LCV histologically. Read More

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http://dx.doi.org/10.1515/jbcpp-2018-0183DOI Listing
July 2019
3 Reads

Propylthiouracil-induced vasculitis in carbimazole-refractory Graves disease.

Med J Aust 2019 06 24;210(11):491-491.e1. Epub 2019 May 24.

Royal North Shore Hospital, Sydney, NSW.

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http://dx.doi.org/10.5694/mja2.50198DOI Listing
June 2019
9 Reads

Colloidal Silver Ingestion Associated with Leukocytoclastic Vasculitis in an Adolescent Female.

Am J Case Rep 2019 May 23;20:730-734. Epub 2019 May 23.

Department of Pediatrics, New York Presbyterian Brooklyn Methodist Hospital, Brooklyn, NY, USA.

BACKGROUND Leukocytoclastic vasculitis is a disease of the small vessels and is uncommon in children. In this case report, we present an adolescent case of leukocytoclastic vasculitis associated with the ingestion of colloidal silver, a naturopathic drug. This report highlights the rarity of the patient's presentation and inducing agent. Read More

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http://dx.doi.org/10.12659/AJCR.915499DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543947PMC
May 2019
23 Reads

Leukocytoclastic vasculitis after vaccination in a patient with inflammatory bowel disease.

Rev Esp Enferm Dig 2019 05;111(5):402-404

Unidad Enf. Inflam. Intest. Servicio de Digestivo., Hospital Universitario Central de Asturias.

Patients with inflammatory bowel disease are likely to receive immunomodulation treatment and therefore, should be properly vaccinated. Despite their proven safety, vaccines are not exempt from adverse reactions. The clinical case was a young female with ulcerative colitis under mesalazine treatment, who developed leukocytoclastic vasculitis following vaccination for pneumococci, varicella and hepatitis A. Read More

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http://dx.doi.org/10.17235/reed.2019.5963/2018DOI Listing
May 2019
11 Reads

Direct Immunofluorescence Results of the Skin Biopsy and Frequency of Systemic Involvement in Children with Henoch-Schonlein Purpura.

Fetal Pediatr Pathol 2019 Apr 2;38(2):121-126. Epub 2019 Jan 2.

b Department of Pathology , Tehran University of Medical Sciences , Tehran , Iran.

Objective: Henoch-Schonlein purpura (HSP) is a common vasculitis in children that can present with multi-organ involvement. The aim of this study is to investigate the correlation between direct immunofluorescence (DIF) results and the systemic involvements of the HSP in pediatric patients.

Material And Methods: Those HSP patients with leukocytoclastic vasculitis on their biopsies who also had documented immunoglobulin/complement deposition by DIF were included in our study. Read More

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http://dx.doi.org/10.1080/15513815.2018.1552733DOI Listing
April 2019
28 Reads

Leukocytoclastic Vasculitis After Influenza Vaccination: An Allergy Assessment.

J Investig Allergol Clin Immunol 2018 Dec;28(6):417-418

Servicio de Enfermedades del Sistema Inmune-Alergia, Hospital Universitario Príncipe de Asturias, Departamento de Medicina y Especialidades Médicas; Universidad de Alcalá, Alcalá de Henares, Madrid, Spain.

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http://dx.doi.org/10.18176/jiaci.0297DOI Listing
December 2018
10 Reads

Purpuric drug eruption without leukocytoclastic vasculitis associated with vancomycin.

Asian Pac J Allergy Immunol 2020 Mar;38(1):47-51

Department of Pediatrics, Yamaguchi University Graduate School of Medicine, 1-1-1 Minamikogushi, Ube, Yamaguchi 755-8505, Japan.

Vancomycin (VCM) has been reported to elicit adverse cutaneous drug reactions. However, VCM-associated purpuric drug eruption has not been reported yet, except leukocytoclastic vasculitis. A 16-year-old Japanese girl was admitted with a respiratory infection. Read More

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http://apjai-journal.org/wp-content/uploads/2018/10/AP-21051
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http://dx.doi.org/10.12932/AP-210518-0319DOI Listing
March 2020
37 Reads
1.255 Impact Factor

Erythema elevatum diutinum a rare and poorly understood cutaneous vasculitis: A single institution experience.

J Cutan Pathol 2019 Feb 3;46(2):97-101. Epub 2018 Dec 3.

Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, Ohio.

Background: Erythema elevatum diutinum (EED) is a rare vasculitis with variable clinical presentation which diagnosis can be challenging. Herein we want to describe the clinicopathological spectrum of findings in five cases of EED.

Methods: We retrospectively analyzed five cases in a single institution collected over a period of 27 years. Read More

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http://doi.wiley.com/10.1111/cup.13378
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http://dx.doi.org/10.1111/cup.13378DOI Listing
February 2019
29 Reads

[Erratum to: Monolocular erythema elevatum diutinum on the back of the hand].

Hautarzt 2018 10;69(10):878

Klinik und Poliklinik für Dermatologie und Allergologie, Ludwig-Maximilians-Universität München, Frauenlobstr. 9-11, 80337, München, Deutschland.

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http://dx.doi.org/10.1007/s00105-018-4242-2DOI Listing
October 2018
8 Reads

[Monolocular erythema elevatum diutinum on the back of the hand].

Hautarzt 2018 Oct;69(Suppl 1):31-33

Klinik und Poliklinik für Dermatologie und Allergologie der Ludwig-Maximilians-Universität München, Frauenlobstr. 9-11, 80337, München, Deutschland.

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http://dx.doi.org/10.1007/s00105-018-4217-3DOI Listing
October 2018
13 Reads

Primary Surgical Treatment of Erythema Elevatum Diutinum.

J Hand Surg Am 2019 Jun 18;44(6):522.e1-522.e5. Epub 2018 Sep 18.

Department of Orthopaedics, Louisiana State University Health Sciences Center, New Orleans, LA.

Erythema elevatum diutinum (EED) is a rare skin disease caused an Arthrus-type immunological reaction to antigen with immune complex deposition in the cutaneous microvasculature, which leads to tissue damage secondary to the effects of complement and leukocytes. It presents as brown or red cutaneous nodules, papules, or plaques, often on the extensor surfaces of the hands, knees, or elbows. Onset usually occurs in the fourth to sixth decades but possibly younger in patients with human immunodeficiency virus. Read More

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http://dx.doi.org/10.1016/j.jhsa.2018.07.018DOI Listing
June 2019
18 Reads

Rare presentation of erythema elevatum diutinum.

JAAD Case Rep 2018 Sep 18;4(8):824-826. Epub 2018 Sep 18.

Dermatology Department, Hôtel-Dieu University Hospital, Nantes, France.

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http://dx.doi.org/10.1016/j.jdcr.2018.05.025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143691PMC
September 2018
15 Reads

A case of Graves' disease associated with membranoproliferative glomerulonephritis and leukocytoclastic vasculitis.

J Pediatr Endocrinol Metab 2018 Oct;31(10):1165-1168

Ghent University, Department of Pediatrics and Medical Genetics, Ghent, Belgium.

Background The association of hyperthyroidism with renal disease is very rare and the importance of timely clinical recognition cannot be overemphasized. Case presentation An 11-year-old girl presented with gastrointestinal symptoms while hypertension, edema and abdominal pain were noticed on clinical examination. Laboratory investigation revealed: hemoglobin 9. Read More

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http://dx.doi.org/10.1515/jpem-2018-0186DOI Listing
October 2018
22 Reads

[Drug-induced vasculitis].

Therapie 2019 Jun 24;74(3):347-354. Epub 2018 Jul 24.

Département de pharmacologie, faculté de médecine de Sousse, université de Sousse, avenue Md Karoui, 4002 Sousse, Tunisie.

Introduction: Drug-induced vasculitis is reported in almost 10-20 % of vasculitis. Several drugs may be incriminated in their occurrence. Our study aimed to study the epidemiological, clinical, histopathological and evolutionary characteristics of drug-indced vasculitis from a series of cases and to specify the different drugs involved. Read More

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http://dx.doi.org/10.1016/j.therap.2018.07.005DOI Listing
June 2019
71 Reads

HIV-associated erythema elevatum diutinum: a case report and review of a clinically distinct variant.

Dermatol Online J 2018 05 15;24(5). Epub 2018 May 15.

Medstar Georgetown University Hospital, Washington, District of Columbia.

A 24-year-old man with untreated human immunodeficiency virus (HIV) infection consulted our outreach clinic owing to the development of numerous asymptomatic nodules on his palms and fingers. Histopathologic evaluation revealed leukocytoclastic vasculitis and prominent fibrosis with a neutrophilic infiltrate consistent with erythema elevatum diutinum (EED). We referred the patient for initiation of antiretroviral therapy and started him on dapsone. Read More

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May 2018
21 Reads

Cutaneous and Gastrointestinal Leukocytoclastic Vasculitis Induced by Palbociclib in a Metastatic Breast Cancer Patient: A Case Report.

Clin Breast Cancer 2018 10 16;18(5):e755-e758. Epub 2018 Aug 16.

Medical Oncology Department, Institut de Cancérologie de l'Ouest, Centre Paul Papin, Angers, France.

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https://linkinghub.elsevier.com/retrieve/pii/S15268209183031
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http://dx.doi.org/10.1016/j.clbc.2018.07.006DOI Listing
October 2018
44 Reads

Colon-Limited Leukocytoclastic Vasculitis.

Am J Gastroenterol 2018 08;113(8):1114

Department of Gastroenterology, Centro Hospitalar Vila Nova de Gaia Espinho, Vila Nova Gaia, Portugal. Department of Pathology, Centro Hospitalar Vila Nova de Gaia Espinho, Vila Nova Gaia, Portugal.

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http://dx.doi.org/10.1038/s41395-018-0081-0DOI Listing
August 2018
5 Reads

Erythema elevatum diutinum: a case report and review of literature.

Int J Dermatol 2019 Apr 3;58(4):408-415. Epub 2018 Aug 3.

The Kimberly and Eric J. Waldman Department of Dermatology and Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Erythema elevatum diutinum (EED) is a rare cutaneous leukocytoclastic vasculitis thought to be related to increased levels of circulating antibodies. It has been shown to be associated with HIV infection, tuberculosis, as well as various autoimmune diseases. A retrospective review of all cases of EED indexed in PubMed between 1990 and 2014 was performed. Read More

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http://dx.doi.org/10.1111/ijd.14169DOI Listing
April 2019
10 Reads

Case 2: Hemolacria, Hematochezia, and Hematuria in an 11-month-old Boy.

Pediatr Rev 2018 Aug;39(8):418-420

Department of Pediatrics, Cohen Children's Medical Center at Northwell Health, New Hyde Park, NY.

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http://dx.doi.org/10.1542/pir.2016-0155DOI Listing
August 2018
10 Reads

Erythema elevatum diutinum.

An Bras Dermatol 2018 Jul-Aug;93(4):614-615

Service of Dermatology, Hospital Guilherme Álvaro, Centro Universitário Lusíada, Santos (SP), Brazil.

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http://dx.doi.org/10.1590/abd1806-4841.20187470DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063113PMC
August 2018
14 Reads

Unusual presentation of erythema elevatum diutinum with underlying hepatitis B infection.

Cutis 2018 Jun;101(6):462-465

Ohio State University Medical Center, Columbus, USA.

Erythema elevatum diutinum (EED) is a rare, chronic, cutaneous small vessel vasculitis of unclear pathogenesis. Classically, lesions present as symmetric red to purple plaques, papules, and nodules overlying joints. First-line therapy is dapsone. Read More

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June 2018
10 Reads

Pyoderma gangrenosum and erythema elevatum diutinum associated with a high-risk myelodysplastic syndrome: case report.

Hematol Transfus Cell Ther 2018 Apr-Jun;40(2):192-195. Epub 2018 Feb 17.

Centro Hospitalar de São João EPE, Porto, Portugal.

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http://dx.doi.org/10.1016/j.htct.2017.11.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001934PMC
February 2018
8 Reads

Erythema elevatum diutinum associated with severe oropharyngeal ulceration and pyoderma gangrenosum.

J Dtsch Dermatol Ges 2018 May;16(5):617-620

Department of Dermatology, Venerology and Allergology, University Hospital Schleswig-Holstein, Campus Kiel, Germany.

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http://dx.doi.org/10.1111/ddg.13508DOI Listing
May 2018
9 Reads

Erythema elevatum diutinum verbunden mit schwerer oropharyngealer Ulzeration und Pyoderma gangraenosum.

J Dtsch Dermatol Ges 2018 May;16(5):616-619

Klinik für Dermatologie, Venerologie und Allergologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Deutschland.

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http://dx.doi.org/10.1111/ddg.13508_gDOI Listing
May 2018
9 Reads

A Case Report and Literature Review of Scrub Typhus With Acute Abdomen and Septic Shock in a Child-The Role of Leukocytoclastic Vasculitis and Granulysin.

Am J Dermatopathol 2018 Oct;40(10):767-771

Department of Dermatology, Chang Gung Memorial Hospital, Linko, Taipei, Taiwan.

Scrub typhus is becoming a clinically important cause of acute undifferentiated febrile illness in Taiwan. The incubation period is between 6 and 21 days after exposure. It is transmitted by chiggers (larva of trombiculid mite) in long grasses and in dirt-floor homes, with infection characterized by a flu-like illness of fever, headache, and myalgia lasting approximately 1 week. Read More

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http://dx.doi.org/10.1097/DAD.0000000000001167DOI Listing
October 2018
22 Reads

Leukocytoclastic Vasculitis and Desensitization to High-dose Methotrexate in Primary Central Nervous System Lymphoma.

Clin Lymphoma Myeloma Leuk 2018 05 19;18(5):e197-e200. Epub 2018 Mar 19.

Department of Hematology-Oncology, Faculty of Medicine, Saint Joseph University, Beirut, Lebanon. Electronic address:

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http://dx.doi.org/10.1016/j.clml.2018.03.008DOI Listing
May 2018
12 Reads

Carbamazepine-induced necrotizing leukocytoclastic vasculitis with a 20-year latency.

G Ital Dermatol Venereol 2018 Apr;153(2):285-286

Department of Dermatology, Faculty of Medicine, Umberto I Polyclinic Hospital, Sapienza University of Rome, Rome, Italy.

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https://www.minervamedica.it/index2.php?show=R23Y2018N02A028
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http://dx.doi.org/10.23736/S0392-0488.16.05490-0DOI Listing
April 2018
16 Reads

Erythema Elevatum Diutinum Treated With Mycophenolate Mofetil.

J Clin Rheumatol 2019 09;25(6):e93-e94

School of Medicine, University of Alabama at Birmingham, Birmingham, AL University of Central Florida, Orlando, FL

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http://dx.doi.org/10.1097/RHU.0000000000000752DOI Listing
September 2019
13 Reads

Complete resolution of erythema elevatum diutinum using oral sulfasalazine.

Dermatol Online J 2017 Oct 15;23(10). Epub 2017 Oct 15.

Harvard University, Cambridge, Massachusetts, Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts. michael_

Erythema elevatum diutinum (EED) is a rare, chronic small-vessel vasculitis that presents as firm, red, violaceous, or brown papules and nodules on the extensor surfaces of the limbs. Oral dapsone is considered first-line therapy for EED; in the current case report, a patient presenting with EED began dapsone treatment and symptoms subsided within two weeks. Seven months later, the patient became pregnant and stopped dapsone owing to her concerns with dapsone use during pregnancy, resulting in recurrence of EED symptoms. Read More

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October 2017
15 Reads

Leukocytoclastic vasculitis associated with rivaroxaban.

Int J Dermatol 2018 05 20;57(5):622-624. Epub 2018 Feb 20.

Department of Dermatology, University Hospital Complex, Santiago de Compostela, Spain.

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http://dx.doi.org/10.1111/ijd.13952DOI Listing
May 2018
16 Reads

Histologic Features of Gastrointestinal Tract Biopsies in IgA Vasculitis (Henoch-Schönlein Purpura).

Am J Surg Pathol 2018 04;42(4):529-533

Departments of Pathology.

Immunoglobulin A (IgA) vasculitis or Henoch-Schönlein purpura (HSP) typically occurs in the pediatric population, although rare cases also occur in adults. Gastrointestinal (GI) involvement is common. The "classic" histologic finding in IgA vasculitis (HSP) is leukocytoclastic vasculitis (LCV); other histologic features in biopsies of IgA vasculitis (HSP) have only been rarely described. Read More

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http://dx.doi.org/10.1097/PAS.0000000000001036DOI Listing
April 2018
30 Reads

Erythema elevatum diutinum-like vasculitis secondary to cocaine adulterated with levamisole.

Clin Exp Dermatol 2018 Jun 9;43(4):494-496. Epub 2018 Feb 9.

Department of Dermatology, Brigham and Women's Hospital, Boston, MA, USA.

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http://dx.doi.org/10.1111/ced.13392DOI Listing
June 2018
10 Reads

Apixaban Causing Leukocytoclastic Vasculitis.

J Allergy Clin Immunol Pract 2018 Sep - Oct;6(5):1744-1745. Epub 2018 Jan 19.

Department of Pathology, Hartford Hospital, East Hartford, Conn.

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http://dx.doi.org/10.1016/j.jaip.2017.12.007DOI Listing
November 2019
6 Reads

Neutrophilic dermatoses: a broad spectrum of disease.

G Ital Dermatol Venereol 2018 Apr 24;153(2):265-272. Epub 2018 Jan 24.

Unit of Dermatology, Carlo Urbai Hospital, AREA Vasta 2 ASUR Marche, Jesi, Ancona, Italy -

The neutrophilic dermatoses (NDs) comprise a group of heterogeneous disorders characterized by inflammatory skin lesions that histologically show an intense inflammatory infiltrate composed primarily by neutrophils, with no evidence of infection or vasculitis. Although there are distinct clinical differences in the classical lesions of these disorders, many patients have overlapping features. In this review, we describe the clinical aspects of the main NDs, including: Sweet Syndrome, ND of the dorsal hands, pyoderma gangrenosum, erythema elevatum diutinum, subcorneal pustular dermatosis, neutrophilic eccrine hidradenitis, rheumatoid neutrophilic dermatitis, neutrophilic panniculitis, and aseptic abscesses including their association with underlying diseases and the differential diagnoses. Read More

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http://dx.doi.org/10.23736/S0392-0488.18.05841-8DOI Listing
April 2018
11 Reads

Late-Stage Erythema Elevatum Diutinum Mimicking a Fibroblastic Tumor: A Potential Pitfall.

Am J Dermatopathol 2018 Jun;40(6):442-444

Dermatopathology Department, Friedrichshafen Dermatopathologie, Friedrichshafen, Germany.

Erythema elevatum diutinum (EED) is a rare dermatosis with evolving histopathological features that vary according to the age of the lesions, with a variable fibrosis and a fascicled proliferation of spindle cells in late phases. The authors present an otherwise healthy 57-year-old woman with multiple indurated nodules on the inner aspect of both feet. Skin biopsy showed storiform interlacing bundles of spindled cells with plump nuclei and some areas with neutrophils and leukocytoclasia. Read More

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http://dx.doi.org/10.1097/DAD.0000000000001088DOI Listing
June 2018
15 Reads

Erythema elevatum diutinum with pustule formation: An unusual finding.

J Cutan Pathol 2018 03 2;45(3):246-248. Epub 2018 Jan 2.

Department of Dermatology, Chinese PLA General Hospital & Medical School, Beijing, China.

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http://dx.doi.org/10.1111/cup.13095DOI Listing
March 2018
15 Reads