Results 131 to 140 of about 157,469 (244)
Early Acitretin Therapy in a Patient With Harlequin Ichthyosis
ABSTRACT Harlequin ichthyosis (HI) is a rare, severe congenital disorder of keratinization caused by pathogenic variants in the ABCA12 gene resulting in thick, hyperkeratotic plates, deep fissures, and characteristic facial and limb abnormalities.
Orasa Sukmark +2 more
wiley +1 more source
Apoptosis in oral erythema multiforme
Objective. Cell death was evaluated in oral erythema multiforme to test the hypothesis that apoptosis may be a mechanism by which keratinocytes die in this condition. Study design.
Dekker, N.P. +4 more
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A Case of Cutaneous B Lymphoblastic Lymphoma With Multiple Cutaneous Tumors
ABSTRACT A 17‐year‐old Japanese male patient was referred to our hospital due to an erythematous tumor on part of the right mandible that had developed 3 months earlier, and similar tumors had appeared on the trunk and lower extremities. A complete blood count showed no specific abnormalities.
Tomomichi Shimizu +4 more
wiley +1 more source
ABSTRACT Differentiation syndrome (DS) and Sweet syndrome (SS) are inflammatory complications mediated by cytokine dysregulation, classically associated with therapies that promote myeloid differentiation or cytokine release. While DS has been primarily linked to all‐trans retinoic acid (ATRA) and IDH inhibitors, recent evidence suggests that ...
Katerina Grafanaki +6 more
wiley +1 more source
Palmar erythema [Palmar eritem]
Palmar erythema is a clinical sign presenting with symetrical erythema of both palms. It is usually asymptomatic and may seldom be seen in healthy individuals. Systemic diseases, drugs, chemicals, neoplasms and infections may play a role in the etiology.
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Eruptive Xanthomas in a Patient With Severe Dyslipidemia
JEADV Clinical Practice, EarlyView.
Michał Niedźwiedź +3 more
wiley +1 more source
Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency
ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz +2 more
wiley +1 more source
(The) clinical and histopathological study of erythema induratum and erythema nodosum
의학과/석사[한글] 경결홍반과 결절홍반은 하지에 염증성 결절이 나타나는 질환으로 임상소견이 각기 다른 특징을 갖는다. 그러나 병변이 두질환 모두 주로 하지에 결절로 나타나고 임상적 변형이 있으며, 병리조직학적 소견상 두 질환 모두 급성, 아급성 흑은 만성 지방층염의 양상을 나타내고, 병의 진행 정도와 조직생검 부위에 따라 각 질환의 병리학적 변화도 다양하게 나타나므로 감별진단이 어려운 경우가 많다.
최은선
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Alopecic Patches on the Extremities of a Young Man
JEADV Clinical Practice, EarlyView.
Hamad El Hajj +3 more
wiley +1 more source
Practice Patterns in Extramammary Paget's Disease
ABSTRACT Background In patients with Extramammary Paget's Disease (EMPD), a rare intraepithelial adenocarcinoma, wide local excision (WLE) has historically been the standard of treatment despite high rates of positive margins and recurrence. Mohs micrographic surgery (MMS) has demonstrated superior outcomes, yet practice patterns vary due to limited ...
Yasmine Mohseni +4 more
wiley +1 more source

