Results 41 to 50 of about 2,001 (196)

Severe cutaneous scleromyxedema treated by lenalidomide

JEADV Clinical Practice, 2023
Scleromyxedema is a rare clinical variant of primary cutaneous mucinosis. It is defined by a generalized papular and sclerodermoid eruption associated with monoclonal gammopathy. No specific definitive treatment is known and those tried have inconsistent
Théo Brochet, Ali Dadban, Quentin Beauvillain, Clemence Boucher, Fanny Dessirier, Christophe Attencourt, Catherine Lok, Pierre Morel, Aurélie Halle, Guillaume Chaby   +9 more
doaj   +1 more source

Oral Focal Mucinosis. [PDF]

Arch Iran Med
Kumar VV, Jangal Krishanappa S, Hemdal Channabasaviah G, Sharad Kamat M, Gowdara Prakash S.   +4 more
europepmc   +3 more sources

Cutaneous mucinosis of infancy

JAAD Case Reports, 2016
We present a case of a 4-year-old fair-skinned girl, with no significant medical history, who presented to the outpatient clinic of an academic medical center with an asymptomatic, flesh-colored, cobblestoned plaque on her lateral left thigh (Fig 1).
Reddy, Swapna C., Baman, Jayson R., Morrison, Clinton S., Scott, Glynis A.   +3 more
openaire   +2 more sources

Skin-Colored Papules on the Face and Chest of a Female Patient. [PDF]

Clin Case Rep
ABSTRACT Scleromyxedema is an unpredictable but progressive disease and can be lethal due to systemic involvement if not diagnosed timely. Hence, we require a keen observational clinical eye to diagnose the condition from its differentials, along with further research into treatment modalities to treat this condition.
Ghahartars M, Azimi SZ, Akbarzadeh Jahromi M, Namazi MR.   +3 more
europepmc   +2 more sources

S3 guideline diagnostics and therapy of alopecia areata – Part 1: Diagnostics and epidemiology

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary In the project funded by the Innovation Committee at the G‐BA, the S3 guideline for the diagnosis and treatment of AA was developed between 2023 and 2025. The interdisciplinary expert panel consisted of representatives from the German Dermatological Society, in particular from the Pediatric Dermatology Working Group, the Professional ...
Ulrike Blume‐Peytavi, Andria Constantinou, Tsenka Tomova‐Simitchieva, Adrian Tanew, Michael Sticherling, Hermann Girschick, Annika Vogt, Uwe Schwichtenberg, Uwe Gieler, André Märtens, Kerstin Zienert, Claudia Stenders, Ricardo Niklas Werner, Doris Wilborn   +13 more
wiley   +1 more source

Scleroderma with Acro-Osteolysis and Papular Mucinosis Resembling [PDF]

, 2020
Objectives: We describe a case of systemic sclerosis (SS) with acro-osteolysis associated with cutaneous mucinosis, usually characterized by mucin deposition in the skin.
Silva de Oliveira, Isabela, Pimenta da Fonseca, Emanuela, Dantas, João, Santiago, Mittermayer B   +3 more
core   +1 more source

#70. Follicular Mucinosis and Cutaneous T-Cell Lymphoma Association: A Clinicopathologic and Molecular Analysis of 19 Cases

Graduate Medical Education Research Journal
Mentor: Safina Hafeez Program: Pathology Type: Original Research Background: Follicular mucinosis is a rare dermatologic disorder characterized by the accumulation of mucin within hair follicles, resulting in distinct skin lesions.
Ahmad Alshomrani, Ketav Desai, Allison Vokoun, Ab Rauf Shah, Ann Crowley, Dinesh Pradhan, Joseph D. Khoury, Safina Hafeez   +7 more
doaj   +1 more source

Clinicopathological features, therapeutic options, and significance of CD103 expression in 15 patients with follicular mucinosis

Frontiers in Medicine, 2023
BackgroundFollicular mucinosis (FM) is generally divided into a primary benign idiopathic form and a secondary form associated with mycosis fungoides.ObjectiveTo analyze the clinical and pathological features of FM and explore the pathological ...
Jiaqi Wang, Yanqing Wang, Hongyu Zhou, Ping Wang, Mengyan Zhu, Liuyu Li, Hong Shen   +6 more
doaj   +1 more source

Anogenital Papular Mucinosis in Chronic Anal Fissures: A Review of a Reactive Mucinous Pattern

Dermatological Reviews, Volume 7, Issue 3, June 2026.
ABSTRACT Background Anogenital papular mucinosis (APM) is a rare localized cutaneous mucinosis characterized by dermal mucin deposition presenting as flesh‐colored papules in the anogenital region. Its rarity and clinical resemblance to common infectious and inflammatory dermatoses contribute to frequent misdiagnosis.
Douglas Jaxon Vadner, Maria Anna Guirguis, Alicia Fields, Felix Bui, Justin Ikara, Stephanie Jackson   +5 more
wiley   +1 more source

Large Oral Focal Mucinosis: A Case Report

, 2015
The aim of this article is to report the case of a 23-year-old female patient that sought dental service for examination of an asymptomatic slow-growing large lump in the mandibular gingiva causing displacement of the right first molar. Excisional biopsy,
Noroes T.S.A., Da Costa Miguel M.C., De Brito Monteiro B.V., Godoy G.P., Da Silva K.R.   +4 more
core   +1 more source