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granulomatosis with polyangiitis/ubi jalar

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Strawberry gingivitis: Challenges in the diagnosis of granulomatosis with polyangiitis on gingival specimens.

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Strawberry gingivitis is a rare oral manifestation of granulomatosis with polyangiitis (GPA, formerly known as Wegener's granulomatosis). It manifests as a red-purple hyperplastic gingivitis that frequently goes unrecognized as a disease-specific symptom, especially if it is the primary and only
Reports of oral manifestations of granulomatosis with polyangiitis usually refer to single-case reports; "strawberry gingivitis" has been increasingly reported.To study the clinicopathological findings of four patients in which the diagnosis of

Strawberry Gingivitis in Granulomatosis with Polyangiitis.

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Strawberry gingival enlargement as only manifestation of Wegeners granulomatosis.

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Strawberry gingivitis as a manifestation of granulomatosis with polyangiitis.

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Strawberry Gingivitis: A rare manifestation of granulomatosis with polyangiitis.

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"Strawberry" gingival hyperplasia: a pathognomonic mucocutaneous finding in Wegener granulomatosis.

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Strawberry gingivitis as the first manifestation of granulomatosis with polyangiitis.

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Image Gallery: Strawberry gingivitis as first sign of granulomatosis with polyangiitis.

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Strawberry gums as an initial presentation of severe granulomatosis with polyangiitis

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Two cases of granulomatosis polyangiitis presenting with Strawberry gingivitis and a review of the literature.

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Hyperplastic gingivitis is a rare manifestation of granulomatosis with polyangiitis (GPA). This gingivitis has a very distinctive clinical appearance (so-called Strawberry gingivitis) and when seen is virtually pathognomic for GPA. Gingivitis often precedes other organ involvement therefore making

Role of gingival manifestation in diagnosis of granulomatosis with polyangiitis (Wegener's granulomatosis).

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OBJECTIVE This report describes a case of granulomatosis with polyangiitis (GPA) in which the gingival manifestation was crucial in both making an early diagnosis and possibly in deciding the approach to treatment. METHODS A 57-year-old sailor presented to the Department of Dentistry at Ulsan
BACKGROUND Granulomatosis with polyangiitis (GPA), formerly referred to as Wegener's granulomatosis, is a rare systemic disease of unknown etiology which can affect all areas of the body, including the oral cavity. The typical oral manifestations occur as nonspecific erosive/ulcerative lesions of

Oral manifestations of granulomatosis with polyangiitis - Clinical and radiological assessment.

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Granulomatosis with polyangiitis (GPA) is a type of primary systemic vasculitis associated with the presence of anti-neutrophil cytoplasmic antibodies (ANCA). GPA mainly affects medium and small vessels and may manifest in different organs, most commonly upper respiratory tract. Oral

Unilateral eyelid edema and mucosal involvement as the first presentations of Wegener granulomatosis.

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Wegener granulomatosis or granulomatosis with polyangiitis is a pauci-immune small vessel vasculitis which is usually associated with anti-neutrophil cytoplasmic antibodies (ANCA) mainly in old men. This small vessel vasculitis is usually characterized by necrotizing granulomatous
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