Results 1 to 10 of about 57,398 (258)
Idiopathic Penile Calcinosis Cutis: A Histopathological Case Report [PDF]
Background and Clinical Significance: Calcinosis cutis is a rare condition that can develop through several mechanisms. These include dystrophic, calciphylaxis (classical, metastatic, and iatrogenic), and idiopathic mechanisms.
George Stoyanov +2 more
doaj +2 more sources
Calcinosis cutis, characterized by the deposition of calcium in the skin or subcutaneous tissue, presents in 5 subtypes: dystrophic calcification, idiopathic calcification, iatrogenic calcification, metastatic calcification, and calciphylaxis.
James F. Howick V +1 more
doaj +2 more sources
Congenital leukemia cutis in an infant
Background: The infiltration of neoplastic leukocytes or their progenitors into the epidermis, dermis, or subcutis, resulting in clinically evident cutaneous lesions, is known as leukemia cutis.
Carol Lobo, J P Prathibha
doaj +1 more source
Cutis Marmorata Telangiectatica Congenita: Case Series and Literature Review [PDF]
Boia M +8 more
europepmc +2 more sources
Cutaneous side effects caused by treatment for inflammatory bowel disease [PDF]
nema
Dino Tarabar +6 more
doaj +1 more source
Context.— Myelodysplasia cutis is an emerging concept in cutaneous neoplasia. Many of these cases were previously included under the umbrella of histiocytoid Sweet syndrome. However, with the advent of next-generation sequencing, cutaneous involvement by myelodysplastic syndrome is being increasingly recognized.
Carli P, Whittington +5 more
openaire +2 more sources
Dystrophic calcinosis cutis in a patient with cutaneous sarcoidosis in remission
A 65‐year‐old Japanese woman was referred to our department because of a 5‐month history of asymptomatic papules on the face. She was diagnosed with cutaneous sarcoidosis on the face 20 years ago.
Miyuki Yoshikawa +3 more
doaj +1 more source
Cutis laxa is an inherited or acquired disease characterized by redundant, sagging and inelastic skin. In inherited cutis laxa an abnormal synthesis of extracellular matrix proteins occurs due to genetic defects coding for diverse extracellular matrix components.
Mohamed, M. +6 more
openaire +2 more sources
Association of amyloidosis cutis dyschromica and familial Mediterranean fever [PDF]
: Amyloidosis cutis dyschromica is a rare type of primary cutaneous amyloidosis characterized by reticulate hyper-pigmentation with discrete hypopigmented macules.
Asli Akin Belli +3 more
doaj +2 more sources
Recognizable neonatal clinical features of aplasia cutis congenita [PDF]
Background: Aplasia cutis congenita (ACC), classified in nine groups, is likely to be underreported, since milder isolated lesions in wellbeing newborns could often be undetected, and solitary lesions in the context of polymalformative syndromes could ...
Antona V. +5 more
core +1 more source

