Bullous Pyoderma Gangrenosum

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منابع مشابه

Fatal bullous pyoderma gangrenosum in a patient with Klinefelter's syndrome.

Sir, Pyoderma gangrenosum (PG) is an idiopathic neutrophilic dermatosis may occur in association with a wide variety of disorders, including inflammatory bowel disease, haematological and rheumatological conditions, and states of perturbed immune function. In addition to the classical ulcerative form of PG, less common variants exist. Among these, bullous PG was first described in 1972 as a pai...

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Bullous pyoderma gangrenosum associated with pancytopenia of unknown origin

Pyoderma gangrenosum (PG) is a neutrophilic dermatosis of unknown origin. Clinically it starts with a pustule, nodule or bulla that rapidly progresses and turns into a painful ulcer with raised, undermined borders. The etiopathogenesis of PG remains unknown. However it is frequently associated with systemic diseases such as inflammatory bowel disease (IBD), haematological disorders or arthritis...

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Bullous pyoderma gangrenosum as a predictor of hematological malignancies*

Pyoderma gangrenosum may precede, coexist or follow diverse systemic diseases. The bullous variety is usually associated with hematologic disorders. From 31 patients with pyoderma gangrenosum diagnosed in our hospital during 10 years, only 2 presented with the bullous type. One patient had previous diagnosis of chronic myeloid leukemia. Both had fast-progressive, painful lesions, and both showe...

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Pyoderma gangrenosum.

Pyoderma gangrenosum (PG) is an idiopathic, ulcerative, noninfective chronic inflammatory skin disorder of unknown etiology. It is associated with systemic medical illness in 50% of cases like inflammatory bowel disease, systemic arthritis, haematological diseases and malignancies. Characteristic lesions begin as pustule or vesiculopustule and progresses to an ulcer or deep erosion with violace...

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Ibrutinib-induced pyoderma gangrenosum.

710 started an oral ibrutinib therapy (3 × 140 mg/d), due to B-CLL. An ulcer biopsy revealed lymphocyte and neutrophil infiltration. No histopathologic signs of carcinoma or vasculitis were observed. After consultation with a hematologist, a tentative diagnosis of ibrutinib-induced pyoderma gangrenosum (PG) was established. In addition to ibrutinib discontinuation, daily prednisone dose was inc...

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ژورنال

عنوان ژورنال: Biomedicine

سال: 2021

ISSN: 0970-2067

DOI: 10.51248/.v41i1.553