Results 21 to 30 of about 30,682 (118)
A Rare Case of Prurigo Pigmentosa in Iranian Sibling Couple. [PDF]
ABSTRACT Prurigo Pigmentosa is a rare inflammatory skin disease of unknown origin, characterized by pruritic, erythematous papules on the chest, back, neck, and anterior abdomen. The eruption resolves with reticular hyperpigmentation that cosmetically affects the patient's quality of life.
Al-Zahawi S +4 more
europepmc +2 more sources
Lupus Erythematosus Tumidus Misdiagnosed as Erythema Nodosum from Coccidioidomycosis [PDF]
Introduction: Lupus erythematosus tumidus (LET) is a rare photosensitive dermatosis that is categorized as intermittent cutaneous lupus erythematosus.
Brianae Garcia +2 more
doaj +2 more sources
Reticular erythematous mucinosis successfully treated with laser in a male patient with systemic lupus erythematosus [PDF]
Takako Miura, Toshiyuki Yamamoto
doaj +2 more sources
Sclerosing diseases of the skin. [PDF]
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Kalantari Y +4 more
europepmc +2 more sources
Cutaneous mucinosis in mixed connective tissue disease* [PDF]
Cutaneous mucinosis is a group of conditions involving an accumulation of mucin or glycosaminoglycan in the skin and its annexes. It is described in some connective tissue diseases but never in association with mixed connective tissue disease.
Maria Helena Sampaio Favarato +5 more
doaj +1 more source
Severe cutaneous scleromyxedema treated by lenalidomide
Abstract 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 results.
Théo Brochet +9 more
wiley +1 more source
Abstract Background Primary cutaneous mucinoses (PCM) are rare diseases characterized by dermal or follicular mucin deposits. Objectives A retrospective study characterizing PCM to compare dermal with follicular mucin to identify its potential origin on a single‐cell level.
S. Steinmann +6 more
wiley +1 more source
Hypersensitivity reactions are common in CLL/SLL patients with CD4+ folliculocentric infiltrates being a potential specific clinicopathologic entity. These hypersensitivity reactions do not appear to be increased in the commonly tested genetic studies for CLL/SLL. Treatment of the underlying lymphoma may alleviate hypersensitivity reactions.
James Abbott +6 more
wiley +1 more source
Trichoepithelioma presenting as leonine facies in a young female
Leonine facies are rare manifestations of Trichoepithelioma where skin‐toned papules are resulting in grooves and fissures on the face. This paper describes a 27‐year‐old woman presented with a painless firm erythematous plaques. The patient presented with leonine facies and was diagnosed with Trichoepithelioma.
Mehdi Ghahartars +3 more
wiley +1 more source
Granulomatous rosacea: Like leukemid in a patient with acute myeloid leukemia [PDF]
Introduction. Skin findings in leukemias may be divided into specific lesions (leukemia cutis) and non-specific lesions (leukemids) which may be found in up to 80% of all patients with leukemias.
Škiljević Dušan +4 more
doaj +1 more source

