617 results match your criteria: "Erythema Elevatum Diutinum"
Erythema Elevatum diutinum - a long-term case series of 10 patients.
Arch Dermatol Res
December 2024
Department of Dermatology, Clinical Unit for Research Trials in Skin, Massachusetts General Hospital, 50 Staniford St, suite 240, Boston, MA, 02114, USA.
Erythema Elevatum Diutinum.
Actas Dermosifiliogr
November 2024
Department of Dermatology, Hospital Universitario y Politécnico La Fe, Valencia, España; Instituto de Investigación Sanitaria (IIS) La Fe, Valencia, España; Universitat de València, Valencia, España.
Erythema elevatum diutinum in a patient with well-controlled Crohn disease.
Dermatol Online J
April 2024
University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Article Synopsis
- Erythema elevatum diutinum is a rare skin condition characterized by long-lasting inflammation of blood vessels and significant scarring in its later stages.
- The article discusses a case involving a 23-year-old woman who has Crohn's disease but was in remission when she developed this skin condition, which is unusual as most cases are associated with active Crohn's.
- This report is important as it highlights a rare presentation of the condition, providing insights for diagnosing and managing similar cases in the future.
Nonbullous Leukocytoclastic Vasculitis in a Patient With Bedbugs.
Am J Dermatopathol
October 2024
Department of Pathology, Quillen College of Medicine, East Tennessee State University, Johnson City, TN; and.
Erythema elevatum diutinum associated with severe ocular complications and lung tuberculosis.
Indian J Dermatol Venereol Leprol
June 2024
Department of Dermatology, The First Hospital of Jilin University, Changchun, Jilin, China.
Erythema Elevatum Diutinum Masquerading as Tinea Imbricata!
Indian J Dermatol
April 2024
From the Department of Dermatology and Venereology, AIIMS, Habibganj, Saketnagar, Bhopal, Madhya Pradesh, India E-mail:
Silodosin-induced leukocytoclastic vasculitis: a first case report.
Eur J Dermatol
February 2024
Department of Pharmacology. Faculty of Medicine, University of Sousse, Tunisia.
Kikuchi-Fujimoto disease associated with a flare-up of a leukocytoclastic vasculitis: A rare case report and review of literature.
Medicine (Baltimore)
March 2024
Department of Internal Medicine, Lebanese Hospital Geitaoui University Medical Center, Beirut, Lebanon.
Article Synopsis
- - Kikuchi-Fujimoto disease (KFD) is a rare cause of cervical lymphadenopathy that often presents with systemic symptoms like fever and rash.
- - A 22-year-old female patient had a flare-up of leukocytoclastic vasculitis complicated by cervical lymphadenopathy, but tests for infections and autoimmune issues returned negative.
- - After an excisional lymph node biopsy confirmed KFD, the patient improved significantly on corticosteroids and showed complete resolution of symptoms after six months; highlighting the need to consider KFD in similar cases.
Cutaneous Leukocytoclastic Vasculitis Induced by the Iodinated Contrast Media Iohexol With Cross-Reactivity to Iodixanol.
J Allergy Clin Immunol Pract
May 2024
Hôpital Maisonneuve-Rosemont, Department of Medicine, Division of Clinical Immunology and Allergy, Université de Montreal, Montreal, Canada. Electronic address:
Ustekinumab-induced leukocytoclastic vasculitis in a young male with Crohn's disease.
Dig Liver Dis
June 2024
Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. Electronic address:
Erythema elevatum diutinum in a patient with rheumatoid arthritis.
Dermatol Online J
October 2023
Centro Universitário do Estado do Pará, Belém, Pará, Brazil.
Article Synopsis
- - Erythema elevatum diutinum (EED) is a rare skin condition characterized by painful, itchy nodular lesions, often associated with other diseases.
- - A case study highlights a 65-year-old woman who experienced such lesions on her elbows, hands, knees, and foot for a year, and a biopsy confirmed the diagnosis of EED.
- - Treatment with dapsone led to significant improvement in her symptoms, emphasizing the importance of recognizing this rare condition to prevent misdiagnosis and ensure timely treatment.
Secondary syphilis presenting as leukocytoclastic vasculitis in a 61-year-old man.
Dermatol Online J
October 2023
Department of Dermatology, Texas A&M College of Medicine-Baylor Scott & White Health, Temple, Texas, USA.
Article Synopsis
- Cutaneous lesions of secondary syphilis are highly infectious and can closely resemble other skin disorders, complicating diagnosis, with rashes typically appearing as non-itchy red to copper-colored spots on various body parts, including palms and soles.
- In a unique case, a 61-year-old man developed a rapidly progressive purpuric rash, accompanied by fatigue and other systemic symptoms, which was initially mistaken for small-vessel vasculitis.
- A detailed examination and skin biopsy ultimately revealed features consistent with secondary syphilis, including the presence of spirochetes and signs of kidney damage linked to IgA nephropathy.
Recurrent Localized Erythema Scarlatiniforme Desquamativum Recidivans Induced by Iodinated Contrast Media.
J Allergy Clin Immunol Pract
May 2024
Service de Pneumologie A, APHP Hôpital Bichat, Paris, France; Université de Paris Cité, Inserm 1152, Paris, France.
Leukocytoclastic Vasculitis Localized to the Uterine Cervix.
Hawaii J Health Soc Welf
March 2024
Department of Obstetrics and Gynecology, Madigan Army Medical Center, Tacoma, WA (SEL, KLL).
Article Synopsis
- - Patients with gynecologic vasculitis need to be assessed for potential systemic diseases, as the treatment and prognosis can change significantly depending on whether the disease is localized or systemic.
- - A case study features a 25-year-old woman who had abnormal cervical screening results and was found to have both cervical dysplasia and leukocytoclastic vasculitis during a colposcopy, alongside a past skin rash that might indicate systemic involvement.
- - The occurrence of leukocytoclastic vasculitis in the uterine cervix may be linked to factors like hormonal contraception and infections (e.g., HPV), emphasizing the importance of monitoring any resulting cervical dysplasia for progression and proper treatment.
Neutrophilic Dermatosis of the Hands: A Case Report.
Acta Dermatovenerol Croat
December 2023
Nooshin Bagherani, MD, PhD, Tehran University of Medical Sciences, Italy Street, Tehran, Iran;
Article Synopsis
- - Neutrophilic dermatosis of the hands (NDDH) is a recently identified localized variant of Sweet's syndrome, characterized by violaceous papulonodules on the hands, lacking true vasculitis findings, as outlined by Strutton et al. (1996) and Galaria et al. (2000).
- - A 46-year-old man presented with a painful, ulcerative lesion on his left hand, which started as a small papule and progressively worsened despite various treatments for suspected bacterial or fungal infections.
- - Upon examination, the lesion measured 4×7 cm and was associated with atrophic scars from previous similar lesions; laboratory tests indicated leukocytosis and altered liver function
Intramedullary leukocytoclastic vasculitis and neutrophil extracellular trap (NET) formation in POEMS syndrome.
Ann Hematol
April 2024
Institute of Pathology, University Hospital Bonn, Bonn, Germany.
Ibrutinib-Associated Leukocytoclastic Vasculitis in a Patient with Chronic Lymphocytic Leukemia.
Turk J Haematol
March 2024
Van Yüzüncü Yıl University Faculty of Medicine, Department of Medical Oncology, Van, Türkiye.
Autophagy during Severe Acute Respiratory Syndrome Coronavirus 2 Induced Leukocytoclastic Vasculitis: New Insights.
J Invest Dermatol
March 2024
Temerty Faculty of Medicine, University of Toronto, Toronto, Canada; Division of Dermatology, Department of Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada; Division of Dermatology, Women's College Hospital, Toronto, Canada. Electronic address:
Acute neutrophilic vasculitis (leukocytoclasia) in 36 COVID-19 autopsy brains.
Diagn Pathol
February 2024
Department of Pathology, Louisiana State University Health Sciences Center, 7th Floor, 2021 Perdido Street, New Orleans, Louisiana, 70112, USA.
Article Synopsis
- COVID-19 is associated with brain morbidity due to factors like hypercytokinemia and immune dysregulation, but there's limited evidence of direct brain infection by the virus itself.
- A study analyzed autopsy data from 36 patients with confirmed SARS-CoV-2 infection, comparing their brain histopathology to control groups, focusing on microcirculatory changes and complement activation.
- Findings revealed that COVID-19 patients exhibited significantly higher levels of acute neutrophilic vasculitis in the brain's microcirculation compared to historical controls, indicating that COVID-19 has distinct pathological effects on the brain’s blood vessels.
Persistent Papules in Erythema Elevatum Diutinum Treated With Dapsone: Challenge.
Am J Dermatopathol
March 2024
Department of Dermatology, SSM Health/Saint Louis University School of Medicine, St. Louis, MO; and.
Persistent Papules in Erythema Elevatum Diutinum Treated With Dapsone: Answer.
Am J Dermatopathol
March 2024
Department of Dermatology, SSM Health/Saint Louis University School of Medicine, St. Louis, MO; and.
Lesional Infiltration of Eosinophils, Basophils, and M2 Macrophages Expressing Eotaxin-1 and Eotaxin-3 in Granuloma Faciale, but not in Erythema Elevatum Diutinum.
Acta Derm Venereol
February 2024
Department of Dermatology, National Defense Medical College, Tokorozawa, Japan.
Accelerating Healing and Relieving Pain: High-Intensity Laser Therapy for Paraneoplastic Cutaneous Vasculitis Associated with Multiple Myeloma.
Am J Case Rep
February 2024
Medical School, Brasília University - Campus Darcy Ribeiro, Brasília, DF, Brazil.
Article Synopsis
- Leukocytoclastic vasculitis (LCV) can be an uncommon skin condition linked to multiple myeloma (MM), which generally leads to a poor prognosis and short survival; different treatments are required for effective management.
- A case involving a 76-year-old woman revealed that LCV was the initial sign of MM, characterized by pain and skin lesions, which were not responsive to standard treatments.
- High-intensity laser therapy (Nd: YAG laser) was implemented, resulting in significant pain relief and complete healing of the patient's lesions after five weeks, highlighting its potential as a non-invasive treatment option.
Erythema Elevatum Diutinum.
Actas Dermosifiliogr
February 2024
Department of Dermatology, Hospital Universitario y Politécnico La Fe, Valencia, Spain; Instituto de Investigación Sanitaria (IIS) La Fe, Valencia, Spain; Universitat de València, Valencia, Spain.
[Immunoglobulin A vasculitis].
Inn Med (Heidelb)
February 2024
Rheumatologie und Immunologie, Kantonsspital Aarau, Tellstraße 25, 5001, Aarau, Schweiz.
Article Synopsis
- Schoenlein-Henoch purpura is a type of immune-mediated small vessel vasculitis that is more common in children, often occurring after upper respiratory infections, while in adults, it presents more severely with a classic set of symptoms including skin, joint, and gastrointestinal issues, as well as kidney involvement.
- The underlying cause of this vasculitis is believed to be changes in the glycosylation of immunoglobulin A (IgA), leading to the formation of immune complexes that trigger inflammation and damage to blood vessels.
- Diagnosis typically involves detecting histological signs of vasculitis and may require kidney biopsies, and treatment focuses on managing symptoms and protecting kidney function, with a need for ongoing medical supervision due