Zobrazeno 1 - 10
of 156
pro vyhledávání: '"W.P. Daniel Su"'
Publikováno v:
New England Journal of Medicine. 347:1412-1418
Pyoderma gangrenosum is a diagnosis of exclusion, and the misdiagnosis of pyoderma gangrenosum can result in substantial complications in patients who have other causes of severe cutaneous ulceration.We reviewed the charts of 240 patients with a diag
Publikováno v:
The Journal of Dermatology. 27:425-433
Two cases of non-familial, late onset (50 and 62-years-old) hyalinosis cutis et mucosae were studied and compared with classical early onset cases. Late onset cases showed essentially the same histological and ultrastructural features described for e
Publikováno v:
Mayo Clinic Proceedings. 74:481-484
Scleromyxedema is a disorder characterized by a typical rash due to the accumulation of mucin in the dermis. It is always associated with a monoclonal protein in the serum and can have a wide variety of systemic manifestations. We describe a 40-year-
Autor:
Roger H. Weenig, W.P. Daniel Su
Publikováno v:
International Journal of Dermatology. 45:1083-1085
Case Report A 68-year-old woman presented with extensive lower-extremity ulceration that had been ongoing and progressivefor 5 months. This process had been attributed to venousinsufficiency with secondary bacterial cellulitis. A biopsyspecimen obtai
Publikováno v:
Journal of the American Academy of Dermatology. 36:970-982
The antiphospholipid syndrome is an acquired multisystem disorder of hypercoagulation, which may be primary or secondary to underlying diseases. Serologic markers for the syndrome are the lupus anticoagulant and anticardiolipin antibodies. Clinical f
Autor:
Arnold L. Schroeter, W.P. Daniel Su, Robert T. Abraham, Katherine K. Lim, Candace J. Sabers, Mark R. Pittelkow
Publikováno v:
Mayo Clinic Proceedings. 71:1182-1191
Treatment with cyclosporine is beneficial for many dermatologic diseases such as psoriasis, lichen planus, Behcet disease, atopic dermatitis, pyoderma gangrenosum, and epidermolysis bullosa acquisita. The selective action of cyclosporine on helper T
Autor:
Mark R. Pittelkow, Doyt L. Conn, W.P. Daniel Su, Ko-Ron Chen, Kristin M. Leiferman, Terry J. George
Publikováno v:
Journal of the American Academy of Dermatology. 35:173-182
Background: Neutrophilic and lymphocytic vascular inflammation is common in vasculitis associated with connective tissue disease (CTD). We recently identified eight patients with CTD and eosinophilic vasculitis. Objective: The purpose of this study w
Autor:
Mark D.P. Davis, W.P. Daniel Su
Publikováno v:
International Journal of Dermatology. 35:240-248
Autor:
W.P. Daniel Su, John L. Snow
Publikováno v:
The American Journal of Dermatopathology. 18:151-155
Clinicopathologic correlation of cutaneous biopsy specimens demonstrating typical lipomembranous fat necrosis was performed. Material from 732 biopsies of various subcutaneous inflammatory disorders seen at our institution in the past 5 years was scr
Publikováno v:
Journal of the American Academy of Dermatology. 34:395-409
Pyoderma gangrenosum (PG) has four distinctive clinical and histologic variants. Some have morphologic and histologic overlapping features with other reactive neutrophilic skin conditions. PG often occurs in association with a systemic disease, and t