2020
DOI: 10.1016/j.ad.2019.02.013
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Dermatosis purpúricas pigmentadas. Revisión de la literatura científica

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Cited by 22 publications
(8 citation statements)
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“… 3 Additional laboratories are recommended to exclude thrombocytopenia, and purpura from other possible causes and autoimmune diseases. 1 , 2 In this case, by clinical presentation, some rashes mimic palpable purpura, and some do not. Together with the patient's vitiligo background, there is a possibility that she might develop another cutaneous autoimmune disease.…”
Section: Discussionmentioning
confidence: 72%
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“… 3 Additional laboratories are recommended to exclude thrombocytopenia, and purpura from other possible causes and autoimmune diseases. 1 , 2 In this case, by clinical presentation, some rashes mimic palpable purpura, and some do not. Together with the patient's vitiligo background, there is a possibility that she might develop another cutaneous autoimmune disease.…”
Section: Discussionmentioning
confidence: 72%
“… 1 Venous hypertension, capillary fragility, and physical activity have been reported as pathogenes of PPD. 1 , 2 Patients can be asymptomatic or have mild itchiness. This patient's cutaneous manifestation is consistent with purpura annularis telangiectodes of Majocchi in which it appears as in reddish‐brown annular patterns, extending peripherally and centrally fading.…”
Section: Discussionmentioning
confidence: 99%
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“…11. Capilaritis congénita (capilaritis de Schamberg), ya que esta entidad es hereditaria con patrón autosómico recesivo, afectando mayormente a hombres y con presentación precoz (2,8).…”
Section: Fuente: Autorunclassified