Results 171 to 180 of about 12,161 (224)
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Familial Cutaneous Mastocytosis

Pediatric Dermatology, 2001
Cutaneous mastocytosis appears to occur sporadically; however, familial inheritance has been reported in 50 families since the mid‐1880s. We report four cases of telangiectasia macularis eruptiva perstans (TMEP) occurring in three generations of a family. Whereas most patients with TMEP manifest in adulthood, all of the members of this family developed
A, Chang   +5 more
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Equine Cutaneous Mastocytosis

Pathologia veterinaria, 1970
A description of equine cutaneous mastocytosis is given. The lesion was characterized by focal aggregates of mast cells, and by eosinophils, fibrinoid necrosis of collagen, and focal necrosis with dystrophic mineralization of necrotic debris. This is an uncommon, previously undescribed lesion in horses.
K, Altera, L, Clark
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Atypical Diffuse Cutaneous Mastocytosis

Archives of Pediatrics & Adolescent Medicine, 1972
A 19-month-old boy was found to have atypical diffuse cutaneous mastocytosis. Although severe dermographism and pressure urticaria were present from early infancy, his disease remained undiagnosed because he lacked the characteristic bullous and pigmented lesions of urticaria pigmentosa and the pebbly skin texture usually found in diffuse cutaneous ...
T, Sahihi, N B, Esterly
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Cutaneous mastocytosis: A dermatological perspective

Australasian Journal of Dermatology, 2020
AbstractMastocytosis is a rare disease characterised by expansion and collection of clonal mast cells in various organs including the skin, bone marrow, spleen, lymph nodes and gastrointestinal tract. The prevalence of mastocytosis has been estimated to be one in 10 000, while the estimated incidence is one per 100 000 people per year.
Di Raimondo, Cosimo   +9 more
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Cutaneous mastocytosis complicating pregnancy

Obstetrics & Gynecology, 1995
Telangiectasia macularis eruptiva perstans, a rare form of cutaneous mastocytosis associated with elevated histamine excretion, has not previously been reported to complicate pregnancy.A woman presented in the late second trimester with an anaphylactoid reaction, rash, uterine contractions, and vaginal bleeding.
J G, Donahue   +2 more
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Cutaneous Mastocytosis – Clinical Heterogeneity

International Archives of Allergy and Immunology, 2002
Cutaneous mastocytosis (CM) encompasses several distinct patterns of disease which can be distinguished by the type of skin lesions, age of onset, familial occurrence, noncutaneous involvement, associated c-kit mutations, and prognosis. A clear distinction of the type of CM in individual patients has important implications regarding patient management ...
Hartmann, Karin, Henz, Beate M.
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Treatment of Cutaneous Mastocytosis

International Archives of Allergy and Immunology, 2002
Therapy of cutaneous mastocytosis is directed towards skin and systemic symptoms due to mediator release and targeted on skin lesions. Symptomatic therapy of cutaneous mastocytosis involves agents that inhibit the release of mediators or antagonize H1 and H2 receptors such as antihistamines ketodifen and Aspirin.
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[Cutaneous mastocytosis].

Annales de dermatologie et de venereologie, 2007
Cutaneous mastocytosis represent the most frequent form of mastocytosis, rare diseases, defined by an abnormal accumulation and proliferation of mastocytes in one or more organs. Cutaneous mastocytosis more often appear early in childhood and usually resolve spontaneously by the time of puberty.
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