Int J Low Extrem Wounds 2020 Jan 29
Livedo Racemosa: Clinical, Laboratory, and Histopathological Findings in 33 Patients.
Pincelli MS, Echavarria AMJ, Criado PR, Marques GF, Morita TCAB, Valente NYS, de Carvalho JF
Livedo racemosa is a cutaneous finding characterized by a persistent, erythematous, or violaceous discoloration of the skin, in a broken, branched, di ...
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Source: PubMed
Semin. Arthritis Rheum. 2019 Dec 28
Polyarteritis nodosa isolated to muscles-A case series with a review of the literature.
Ganeshanandan LR, Brusch AM, Dyke JM, McLean-Tooke APC
Muscular polyarteritis nodosa where disease is isolated to skeletal muscle is a rare and often poorly recognised clinical entity. Patients typically p ...
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Source: PubMed
Turk. J. Pediatr.
Atypical phenotype of an old disease or typical phenotype of a new disease: deficiency of adenosine deaminase 2.
Çakan M, Aktay-Ayaz N, Karadag SG, Tahir-Turanli E, Stafstrom K, Bainter W, Geha RS, Chou J
Çakan M, Aktay-Ayaz N, Karadag SG, Tahir-Turanli E, Stafstrom K, Bainter W, Geha RS, Chou J. Atypical phenotype of an old disease or typical phenotype ...
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Source: PubMed
An Bras Dermatol 2019 Nov 22
Is macular lymphocytic arteritis limited to the skin? Long-term follow-up of seven patients.
Morita TCAB, Trés GFS, Criado PR
Macular lymphocytic arteritis most commonly presents as hyperpigmented macules on the lower limbs. The pathogenesis of this disease is still unclear a ...
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Source: PubMed
Reumatologia
Cutaneous polyarteritis nodosa in a 7-year-old boy: difficulties in diagnosis.
Dybowska-Golota I, Krajewska-Wlodarczyk M, Zuber Z
Vasculitides are a diverse group of diseases. The potential diversity of their clinical symptoms requires the exclusion of other systemic connective t ...
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Source: PubMed
