Results 151 to 160 of about 1,637 (201)

Febrile neutrophilic dermatosis in acute myelogenous leukemia

Cancer, 1976
Three patients with acute myelogenous leukemia and adequate granulocyte reserves developed fever and painful indurated erythematous plaques on their extremities and faces. The plaques became studded with vesicles or bullae and occasionally became necrotic.
J C, Klock, R L, Oken
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Acute febrile neutrophilic dermatosis.

American family physician, 1989
Acute febrile neutrophilic dermatosis, or Sweet's syndrome, usually occurs in middle-aged women with a preceding upper respiratory tract infection. In about 20 percent of reported cases, the syndrome is associated with an underlying malignancy, most frequently acute myelogenous leukemia.
P R, Cohen, L, Almeida, R, Kurzrock
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Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome)

Archives of Dermatology, 1971
A second case of Sweet's syndrome occurred in a male; it is the 20th to appear in the literature. Tender, red plaques in centrifugal distribution appeared in association with fever, leukocytosis, and an elevated erythrocyte sedimentation rate. The process represents an inflammatory vascular reaction pattern of unknown etiology with pathologic changes ...
G C, Goldman, S L, Moschella
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FURTHER OBSERVATIONS ON ACUTE FEBRILE NEUTROPHILIC DERMATOSIS

British Journal of Dermatology, 1968
SUMMARY.— Some points of interest are discussed from studies of 4 more cases of acute febrile neutrophilic dermatosis, including the histology of a very early lesion. The belated recognition of similar microscopical appearances in a striking, localized lesion on a lady's face led to her successful treatment.
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Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome)

Archives of Dermatology, 1984
A 33-year-old woman had many tender, erythematous and pustular plaques on her face, neck, and extremities. Biopsy findings were consistent with a diagnosis of Sweet's syndrome. A chemotaxis test disclosed increased chemotactic activity of the peripheral blood polymorphonuclear neutrophil leukocytes. The patient was successfully treated with dapsone. To
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Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome)

Archives of Dermatology, 1989
• A 58-year-old woman suffering from rheumatoid arthritis complicated by a leukocytoclastic vasculitis had an acute febrile neutrophilic dermatosis (Sweet's syndrome) develop immediately after worsening of her arthritic condition. This association supports the hypothesis that immunologic abnormality is involved in the pathogenesis of Sweet's syndrome ...
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Sweet's Syndrome (Acute Febrile Neutrophilic Dermatosis)

Archives of Dermatology, 1971
The second male patient with classical Sweet's syndrome (acute febrile neutrophilic dermatosis) is reported and the 17 previously published cases are reviewed. All of the present patient's signs and symptoms were dramatically controlled with orally administered prednisone, but temporarily recurred when treatment was discontinued prematurely.
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Acute Febrile Neutrophilic Dermatosis (Sweet Syndrome)

Archives of Dermatology, 1975
• We describe the third reported case of acute febrile neutrophilic dermatosis (Sweet syndrome) in the United States. In the majority of reported cases, the patients were female. However, in our case and in the two cases reported previously in the United States, the patients were male.
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[Acute febrile neutrophilic dermatosis - Sweet's syndrome].

Acta reumatologica portuguesa, 2009
In Rheumatology there are several diseases that frequently develop cutaneous manifestations creating diagnostic difficulties. The Sweet's syndrome appears as archetype of the neutrophilic dermatosis,which is a group of not infectious illnesses, characterized for a dermic neutrophilic and angiocentric infiltrated. The four main features that define this
Ana, Ribeiro, José, Costa, Mónica, Bogas, Lúcia, Costa, Domingos, Araújo   +4 more
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[Acute febrile neutrophilic dermatosis (Sweet syndrome)].

Zeitschrift fur Hautkrankheiten, 1988
6 own patients including atypical cases of Sweet's syndrome are presented; iodide and colchicine were an effective treatment.
L, Török, K, Seres
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