Results 41 to 50 of about 13,834 (202)

Erythema nodosum migrans successfully treated with indomethacin: A rare entity

open access: yesAdvanced Biomedical Research, 2014
Erythema nodosum migrans (subacute nodular migratory panniculitis) is a panniculitis characterized by migrating subcutaneous nodules or plaque on the lower extremity.
Fatemeh Mokhtari   +2 more
doaj   +1 more source

Sarcoidosis in children is an extremely rare disease. The artSarcoidosis in children: rare but possible. A clinical case of 5 years observation of a child having generalized sarcoidosis

open access: yesКлинический разбор в общей медицине, 2022
Sarcoidoicle presents a clinical case of 5 years observation of a child with generalized sarcoidosis from 11 to 16 years old. The disease debuted with erythema nodosum of the legs, weakness.
Alexandra Yu. Simonova   +5 more
doaj   +1 more source

Bispecific Dual‐Immune Checkpoint Inhibitor Associated Cutaneous Toxicity: A Report of Lorigerlimab Adverse Skin Reaction in Two Cancer Patients

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Lorigerlimab is a dual bispecific antibody (BsAb) targeting cytotoxic T‐lymphocyte‐associated protein 4 and programmed cell death protein 1 that is used for treatment of advanced solid cancers such as metastatic castration‐resistant prostate carcinoma.
Niloofar Sina   +5 more
wiley   +1 more source

A retrospective study of the severe and uncommon variants of erythema nodosum leprosum at a tertiary health center in central India

open access: yesInternational Journal of Mycobacteriology, 2019
Background: Erythema nodosum leprosum (ENL) classically presents with tender, coppery, evanescent nodules along with constitutional features and visceral involvement.
Vaishali H Wankhade   +4 more
doaj   +1 more source

Erythema nodosum as Leprosy reaction

open access: yesVestnik Dermatologii i Venerologii, 2020
Purpose.To present a clinical case of leprosy exacerbation on the background of ongoing therapy. Materials and methods.A 52-year-old patient with a diagnosis of "lepromatous (cutaneous) leprosy, leprosy LL" (multi-bacterial leprosy, lepromatous form ...
Viktoria G. Semenova   +2 more
doaj   +1 more source

S1‐Guideline for diagnosis and therapy of necrobiosis lipoidica

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Necrobiosis lipoidica (NL) is a rare granulomatous skin disease of unknown etiology that occurs frequently in association with diabetes mellitus and other comorbidities. The predilection site is the lower leg, particularly the pretibial areas. The exact pathogenesis remains unclear.
Cornelia Erfurt‐Berge   +6 more
wiley   +1 more source

Epidemiology and Genetics of Rheumatic Diseases Suggest a Constant Rate of DNA Damage as Underlying Cause

open access: yesImmunology, EarlyView.
A constant rate of DNA damage that is not perfectly repaired will cause a constant rate of DNA mutations. The chance of mutation will increase if DNA is prone to damage, such as occurs in somatic hypermutation (SHM) hotspots and GC‐rich DNA. Thus, if one mutation‐prone DNA site drives disease, the age of onset of disease and degree of penetrance should
Piet C. de Groen
wiley   +1 more source

Highly suspected valsartan-induced chronic erythema nodosum migrans in a patient with hypertension: a case report

open access: yesJournal of International Medical Research, 2022
Erythema nodosum migrans (ENM) is usually considered as a rare clinical variant of erythema nodosum and is characterized by unilateral, migratory, relatively painless, nodular lesions.
Yong Liu   +3 more
doaj   +1 more source

TNF Inhibitor‐Induced Sarcoidosis‐Like Lesions in Inflammatory Bowel Disease

open access: yesUnited European Gastroenterology Journal, Volume 14, Issue 1, February 2026.
ABSTRACT Background While tumor necrosis factor (TNF) inhibitors can induce paradoxical reactions, sarcoidosis‐like disease has hardly been reported so far. This study aimed to describe the epidemiological, diagnostic and therapeutic features of TNF inhibitor‐induced sarcoidosis‐like lesions in patients with inflammatory bowel disease.
Zlata Chkolnaia   +12 more
wiley   +1 more source

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