Results 121 to 130 of about 27,354 (241)

Evaluation of Hsp70 and Apoptotic Markers in Canine Cutaneous Lupus Erythematosus. [PDF]

Vet Sci
Magi GE, La Gamba G, Mariotti F, Biagini L, Rossi G, Di Cerbo A.   +5 more
europepmc   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1850-1855, August 2026.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi, Michael Kutsche, Helena Lichtenfeld, Fanny Kortüm, Angela Abicht, Laura Herrmann, Theresia Herget   +6 more
wiley   +1 more source

Chilblain lupus: A rare form of cutaneous lupus erythematosus - A case report. [PDF]

SAGE Open Med Case Rep
Perazzolli G, Banchetti E, Melis E, Carletto A, Girolomoni G, Gisondi P.   +5 more
europepmc   +1 more source

An Overview of the Pathogenesis of Cutaneous Lupus Erythematosus. [PDF]

J Clin Med
Verdelli A, Barletta E, Mariotti EB, Landini S, Magnatta A, Ruffo di Calabria V, Corrà A, Quintarelli L, Bonanni I, Sanna L, Corti V, Caproni M.   +11 more
europepmc   +1 more source

Linear cutaneous lupus erythematosus/discoid lupus erythematosus in an adult [PDF]

Advances in Dermatology and Allergology, 2017
Mao, Qiu-Xia, Zhang, Wan-Lu, Wang, Qiang, Xiao, Xue-Min, Chen, Hao, Shao, Xue-Bao, Jia, Hong, Feng, Su-Ying, Wu, Jian-Bing, Li, Cheng-Rang   +9 more
openaire   +2 more sources

Overlap of Primary Biliary Cholangitis and Systemic Sclerosis: A Case of Reynolds Syndrome

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Reynolds Syndrome should be suspected in CREST patients with persistent cholestatic liver enzymes, since delayed diagnosis allows portal hypertension and variceal bleeding to develop. Early anti‐mitochondrial antibody screening and prompt ursodeoxycholic acid therapy improve outcomes, and these patients need multidisciplinary follow‐up for ...
Ali Gohar, Ira Abid, Syeda Eman Fatima, Abdum Muneeb Sandhu, Zain Fatima, Humayun Nasir, Fatima Arshad, Abdul Rehman Shahid Khan, Muhammad Husnain Ahmad, Masab Ali   +9 more
wiley   +1 more source

Cutaneous lupus erythematosus - from pathogenesis to targeted therapy. [PDF]

Nat Rev Rheumatol
Klein B, Billi AC, Abernathy-Close L, Kahlenberg JM.   +3 more
europepmc   +1 more source

Hand Lesions as a Diagnostic Clue in Unexplained SIADH

Clinical Case Reports, Volume 14, Issue 8, August 2026.
Chilblain‐like hand lesions in a patient with otherwise unexplained SIADH prompted evaluation for autoimmune connective tissue disease. (A) Hand lesions before treatment. (B) Marked improvement after topical difluprednate therapy. (C) Skin biopsy showing basal liquefaction/interface change with superficial perivascular lymphocytic infiltration.
Nobuko Watanabe, Takuya Omura, Takahiro Kamihara, Taiki Sugimoto, Jun Matsumoto, Tomomi Omura, Masaki Hasegawa, Mariko Shimono, Zenzo Isogai   +8 more
wiley   +1 more source

Upregulated GLUT1 expression correlates with type I interferon activity and disease severity in cutaneous lupus erythematosus. [PDF]

J Transl Autoimmun
Bokor LA, Szabolcs BL, Király Z, Mohos A, Szepesi Á, Varga V, Sebestyén A, Kemény LV, Holló P, Hidvégi B.   +9 more
europepmc   +1 more source

Ciprofloxacin‐Induced Near‐Total Toxic Epidermal Necrolysis Complicated by Upper Gastrointestinal Bleeding: A Case Report With ALDEN‐Based Causality Assessment

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Toxic epidermal necrolysis (TEN) is a rare but life‐threatening mucocutaneous adverse drug reaction characterized by widespread epidermal necrosis and detachment with significant mucosal involvement. We report a case of near total (80%–90%) body surface area TEN in a previously healthy 30‐year‐old man that developed approximately 5 days after ...
Amanuel D. Wakoya, Alemu B. Mesekere, Seid A. abdullahi, Misale B. Tesfaye, Zeynu H. Endris, Zelalem G. Demissie, Tibebu G. Haile   +6 more
wiley   +1 more source