A young woman with episodic angioedema, papilledema, and eosinophilia

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منابع مشابه

Episodic angioedema associated with eosinophilia*

We report a 12-year-old girl who presented with recurrent angioedema on the face, trunk, and extremities, and concomitant marked weight gain for 5 years. During the episode, her white blood cell count increased to 47.7×109/L with 89.9% eosinophils, followed by elevated serum level of IL-5, IgE, IgM, and LDH. Histopathology showed perivascular eosinophilic infiltration and diffuse eosinophilic i...

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Non-episodic angioedema associated with eosinophilia.

To cite: Shikino K, Hirose Y, Nakagawa S, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2016217428 DESCRIPTION A 26-year-old woman presented with a 1-week history of peripheral oedema, fever and polyarthralgia. Physical examination revealed symmetrical nonpitting oedema of her hands and legs (figure 1). Her medical history was unremarkable. Laboratory fin...

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A dramatic case of non-episodic angioedema with eosinophilia

Gleich Syndrome, also known as episodic angioedema with eosinophilia, was first described in 1984 by Gleich et al as a rare cause of hypereosinophilia. Angioedema with eosinophilia can be classified into 2 types: episodic or non-episodic. We present a dramatic case of non-episodic angioedema with eosinophilia in a young male. A 34 year old construction worker, presented to the emergency departm...

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A young woman with multiple hypopigmented patches

A 33–year-old woman was visited at the dermatological clinic of Loghman-e-Hakim Hospital with multiple hypopigmented patches on her right arm, buttocks and flanks. Her lesions developed over the past year with no regression. Lesions were resistant to multiple antifungal therapies. Clinical examination revealed multiple circular or oval patches on the right arm, flank and sacral area. There was ...

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Episodic angioedema with eosinophilia (Gleich’s syndrome) is a multilineage cell cycling disorder

Episodic Angioedema with Eosinophilia (Gleich’s Syndrome) is a rare disorder characterized by episodes of angioedema and eosinophilia that occur at monthly intervals and resolve spontaneously without therapy. Despite the striking periodicity of this disorder, its similarity to other cyclic hematopoietic disorders with multilineage involvement has not been assessed. To characterize the involveme...

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ژورنال

عنوان ژورنال: American Journal of Hematology

سال: 2009

ISSN: 0361-8609,1096-8652

DOI: 10.1002/ajh.21584