Results 41 to 50 of about 11,390 (180)

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

Clinicopathological Features of Lupus Erythematosus Panniculitis (LEP): A Retrospective Analysis of 54 Cases

open access: yesHealth Science Reports, Volume 9, Issue 8, August 2026.
ABSTRACT Background Lupus Erythematosus Panniculitis (LEP) is a rare subtype of Cutaneous Lupus Erythematosus. It is a challenging disease to diagnose and treat due to limited understanding of its clinical and histopathological characteristics. Methods We conducted a retrospective review of 54 biopsy‐proven LEP cases evaluated at a dermatology referral
Maryam Nasimi   +7 more
wiley   +1 more source

Targeting fibrosis in the treatment of lower urinary tract dysfunction

open access: yesThe Journal of Pathology, Volume 269, Issue 4-5, Page 493-503, August 2026.
Abstract Benign prostatic hyperplasia (BPH) is a widely prevalent age‐associated disease that is the main contributor to lower urinary tract dysfunction (LUTD) in aging men. Although prostate fibrosis has been recognized as a contributor to BPH pathophysiology, there are not any clinically available therapeutics that target this aspect of disease ...
Ajinkya R Limkar   +6 more
wiley   +1 more source

Etanercept in erythema nodosum leprosum [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2017
: One of the biggest challenges in treating leprosy is the control of reaction events. Patients with lepromatous leprosy may present reaction type II, or erythema nodosum leprosum, during treatment, and this reaction can remain in a recurrent form after ...
Julia Rocha Silva Santos   +3 more
doaj   +2 more sources

Carotid Artery Dissection as Initial Manifestation of Overlapping Sarcoidosis and Antiphospholipid Syndrome in a Young Woman

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
Brain MRI demonstrating left hemispheric watershed infarctions and CTA showing high‐grade left internal carotid artery dissection with complete radiological resolution on follow‐up imaging.
Mohammad Ahmad Al‐Jazi   +2 more
wiley   +1 more source

Acute pancreatitis as the first manifestation of duodenal MALT lymphoma

open access: yesBiomedical Papers, 2015
Background: Possibly any tumor that can cause mechanical obstruction of the distal bile duct can induce acute pancreatitis. However, acute pancreatitis as the first clinical manifestation of duodenal lymphoma is extremely rare.
Ivona Simkova   +7 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

Finger Allergic Contact Dermatitis by Proxy Induced by Feline Thiamazole Cream

open access: yes
Contact Dermatitis, EarlyView.
Gabriela Blanchard   +4 more
wiley   +1 more source

Mucocutaneous‐Predominant Pediatric Behçet's Disease With Recurrent Oral and Genital Ulceration: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT A 12‐year‐old boy presented with recurrent oral and scrotal ulcers, papulopustular lesions, arthralgia, and a positive pathergy test. Autoimmune tests were negative; ophthalmologic and gastrointestinal assessments were reassuring. Topical therapy and colchicine produced sustained improvement.
Fares Basel Abu Taha   +8 more
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

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