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Atypical Presentation of Adult-Onset Hydroa Vacciniforme with Direct Immunofluorescence Positivity-A Case Report.
Indian Dermatol Online J
October 2024
Department of Dermatology Venereology and Leprosy, Kalinga Institute of Medical Sciences (KIMS), KIIT Deemed to be University, Bhubaneswar, Odisha, India.
Two cases of hydroa vacciniforme lymphoproliferative disorder in elderly patients: Excellent response to narrow-band ultraviolet B phototherapy.
JAAD Case Rep
January 2025
Department of Dermatology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Systemic hydroa vacciniforme lymphoproliferative disorder in a patient with chronic active EBV infection.
BMJ Case Rep
December 2024
Dermatology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA
Hydroa vacciniforme lymphoproliferative disorders (HVLPD) fall within the clinical spectrum of chronic active epstein barr virus (EBV) disease (CAEBVD), ranging from localised and/or indolent forms (classic HVLPD) to systemic disease with fever, hepatosplenomegaly and lymphadenopathy (systemic HVLPD). A preadolescent male with 47XYY, multicystic dysplastic kidney, autism spectrum disorder and Attention-deficit/hyperactivity disorder (ADHD) presented with photodistributed non-pruritic, non-painful necrotic papulovesicles accompanied by non-febrile intermittent fatigue and lymphadenopathy. The patient had a history of EBV pneumonia in infancy confirmed by CT scan and was later diagnosed with CAEBV.
View Article and Find Full Text PDFA Fatal Case of Severe Leg Edema and Necrotic Ulcers in a 14-Year-Old Boy.
Cureus
September 2024
Service of Dermatology, General Hospital of Mexico "Dr. Eduardo Liceaga", Mexico City, MEX.
Article Synopsis
- A 14-year-old boy was initially diagnosed with Henoch-Schonlein vasculitis due to symptoms like swelling and leg ulcers, but further testing revealed a different condition.
- After undergoing multiple biopsies, he was diagnosed with hydroa vacciniforme-like lymphoproliferative disorder, characterized by Epstein-Barr virus involvement.
- Unfortunately, his parents refused treatment, and he died a few months later, highlighting a rare case where the disease's symptoms first appeared in the legs instead of the face, complicating diagnosis.
[Late-onset hydroa vacciniforme-like lymphoproliferative disorder].
Dermatologie (Heidelb)
October 2024
Klinik und Poliklinik für Dermatologie und Allergologie, Klinikum der Universität München, LMU München, Frauenlobstr. 9-11, 80337, München, Deutschland.
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