Vasculitis and Neutrophilic Vascular Reactions

Barham, Kelly L.; Jorizzo, Joseph L.; Grattan, B.; Cox, N.H.

doi:10.1002/9780470750520.ch49

Cited by 24 publications

(26 citation statements)

References 409 publications

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“…[1–5] It has been described mainly under three headings. Idiopathic or classical SS, SS associated with a malignancy and SS associated with drug intake.…”

Section: Discussionmentioning

confidence: 99%

Recurrent bilaterally symmetrical bullous sweet′s syndrome: A rare and confusing entity

Verma

2012

Indian J Dermatol

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A rare presentation of Sweet's syndrome (SS) (acute febrile neutrophilic dermatosis) is being reported in a 28-year-old man from India. I report a rare presentation of SS that consisted of bilaterally symmetrical, bullous lesions on both forearms with a seasonal recurrence. A thorough work-up for the usual conditions predisposing to or leading to SS did not throw any light on the etiology. After failing treatment with prednisolone alone we added indomethacin, and he responded to the combination in a matter of days with complete clearance of lesions.

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“…[1–5] It has been described mainly under three headings. Idiopathic or classical SS, SS associated with a malignancy and SS associated with drug intake.…”

Section: Discussionmentioning

confidence: 99%

Recurrent bilaterally symmetrical bullous sweet′s syndrome: A rare and confusing entity

Verma

2012

Indian J Dermatol

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“…Based on the clinical presentation, an attempt was made to classify vasculitis as per updated Gilliam's classification. [7] The patients with thrombocytopenia (<50, 000/mm 3 ) and disorders of coagulation; and patients on warfarin/heparin and patients with age of last appeared lesion more than 48 h were excluded from the study.…”

Section: Methods Methodsmentioning

confidence: 99%

Cutaneous vasculitides: Clinico-pathological correlation

Gupta

Handa

Kanwar

et al. 2009

Indian J Dermatol Venereol Leprol

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Leukocytoclastic vasculitis was the commonest type of vaculitis presenting to the dermatology outpatient department. The workup of patients with cutaneous vasculitis includes detailed history, clinical examination and investigations to rule out multisystem involvement followed by skin biopsy and DIF at appropriate stage of evolution of lesions. Follow up of these patients is very essential as cutaneous manifestations may be the forme fruste of serious systemic involvement.

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“…Noteworthy, in Sweet syndrome associated with hematologic malignant neoplasms, the infiltrate may also consist of immature myeloid or leukemic cells. 16,17 In our review of the English-language literature, including major textbooks, 14,15 we were unable to find a description of Sweet syndrome of similar extent as in our patients. The severe widespread, relapsing eruption made us consider the possibility of an as-yet unrecognized novel variant of Sweet syndrome associated with giant cellulitislike plaques.…”

Section: Casementioning

confidence: 60%