نتایج جستجو برای: pigmented purpuric dermatoses

تعداد نتایج: 10267  

Journal: :Archives of Pediatrics & Adolescent Medicine 1915

2016
Alexander KC Leung Amy AM Leung Benjamin Barankin

Schamberg disease, also known as Schamberg purpura or progressive pigmentary purpura, is characterized by orange-brown or reddish-brown macules/patches with overlaying purpuric spots simulating “cayenne pepper”. We report a 54-year-old Chinese woman with Schamberg disease presenting with purpuric macules and patches of varying sizes on the ankles, legs, and knees. The lesions were nonblanchable...

Journal: :Journal of clinical microbiology 1988
K Irino F Grimont I Casin P A Grimont

The rRNA gene restriction patterns of 92 isolates of Haemophilus influenzae biogroup aegyptius, associated with conjunctivitis or Brazilian purpuric fever in the State of São Paulo, Brazil, were studied with 16 + 23S rRNA from Escherichia coli as a probe. All strains were classified into 15 patterns. Isolates from Brazilian purpuric fever cases were seen only in patterns 3 (most frequently) and...

2015
Tueboon Sriphojanart Vasanop Vachiramon

Diffuse dermal angiomatosis (DDA) is a benign, acquired, reactive vascular proliferation. DDA is clinically characterized by painful purpuric plaque with central ulceration. The histopathologic hallmark is diffuse proliferation of endothelial cells that are arranged interstitially between collagen bundles of the reticular dermis. DDA has been reported in association with peripheral atherosclero...

Journal: :BioMed Research International 2013

Journal: :The Southeast Asian journal of tropical medicine and public health 2006
Susheera Chatproedprai Pitirat Boonsuk Siriwan Wananukul Yong Poovorawan Usa Thisyakorn

An 8-month-old girl presented with fever, rash, and diarrhea. Physical examination revealed multiple well-circumscribed, brownish-black, purpuric-like rashes on the face, arms, and legs with cervical and suboccipital lymphadenopathy. Laboratory findings showed mild anemia with thrombocytopenia and positive polymerase chain reaction for parvovirus 819 DNA in the serum. The patient recovered unev...

Journal: :The Netherlands journal of medicine 2003
E M G Jacobs A Hartkamp H A H Kaasjager

A 36-year-old woman presented at our clinic with symmetrical, tender, palpable purpuric lesions on her lower legs and buttocks after restarting PTU therapy for relapsing Graves' disease. PTU-induced vasculitis was diagnosed with remarkable ANCA anti-MPO and anti-PR3 antibody positivity. The purpuric skin lesions resolved immediately after discontinuation of the drug and the ANCA titres lowered....

Journal: :Occupational Medicine 2004

Journal: :Journal of the Portuguese Society of Dermatology and Venereology 2011

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